Linked Data
ClinVar Variation Id:
127831
dbSNP Id:
rs587780078
ExAC:
1:45797186 T / TCC
gnomAD v2:
1-45797186-T-TCC
gnomAD v3:
1-45331514-T-TCC
gnomAD v4:
1-45331514-T-TCC
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.45331516_45331517dup , CM000663.2:g.45331516_45331517dup | GRCh38 |
| NC_000001.10:g.45797188_45797189dup , CM000663.1:g.45797188_45797189dup | GRCh37 |
| NC_000001.9:g.45569775_45569776dup | NCBI36 |
| NG_008189.1:g.13955_13956dup , LRG_220:g.13955_13956dup |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000412971.6:c.759_760dup | ENSP00000410263.2:p.Glu254GlyfsTer? | |
| ENST00000435155.2:c.1176_1177dup | ENSP00000403655.2:p.Glu393GlyfsTer? | |
| ENST00000467459.6:c.*5_*6dup | ENSP00000435889.2:n.*5_*6dup | |
| ENST00000483127.2:c.1161_1162dup | ENSP00000436469.2:p.Glu388GlyfsTer? | |
| ENST00000485271.6:c.1143_1144dup | ENSP00000431264.2:p.Glu382GlyfsTer? | |
| ENST00000529892.6:c.996_997dup | ENSP00000432528.2:p.Glu333GlyfsTer? | |
| ENST00000533178.6:c.*472_*473dup | ENSP00000436430.2:n.*472_*473dup | |
| ENST00000672314.2:c.1143_1144dup | ENSP00000500828.2:p.Glu382GlyfsTer? | |
| ENST00000710952.2:c.1227_1228dup MANE Plus Clinical | ENSP00000518552.2:p.Glu410GlyfsTer? | |
| ENST00000672818.3:c.1218_1219dup | ENSP00000500891.1:p.Glu407GlyfsTer? | |
| ENST00000456914.7:c.1143_1144dup MANE Select | ENSP00000407590.2:p.Glu382GlyfsTer? | |
| ENST00000671898.1:c.1731_1732dup | ENSP00000499896.1:p.Glu578GlyfsTer? | |
| ENST00000672011.1:c.*472_*473dup | ENSP00000500418.1:n.*472_*473dup | |
| ENST00000672314.1:c.1143_1144dup | ENSP00000500828.1:p.Glu382GlyfsTer? | |
| ENST00000672593.1:c.*1369_*1370dup | ENSP00000500455.1:n.*1369_*1370dup | |
| ENST00000672818.2:c.1218_1219dup | ENSP00000500891.1:p.Glu407GlyfsTer? | |
| ENST00000673134.1:c.*840_*841dup | ENSP00000500526.1:n.*840_*841dup | |
| ENST00000354383.10:c.1146_1147dup | ENSP00000346354.6:p.Glu383GlyfsTer? | |
| ENST00000355498.6:c.1143_1144dup | ENSP00000347685.2:p.Glu382GlyfsTer? | |
| ENST00000372098.7:c.1218_1219dup | ENSP00000361170.3:p.Glu407GlyfsTer? | |
| ENST00000372104.5:c.1143_1144dup | ENSP00000361176.1:p.Glu382GlyfsTer? | |
| ENST00000372110.7:c.1188_1189dup | ENSP00000361182.3:p.Glu397GlyfsTer? | |
| ENST00000372115.7:c.1185_1186dup | ENSP00000361187.3:p.Glu396GlyfsTer? | |
| ENST00000448481.5:c.1176_1177dup | ENSP00000409718.1:p.Glu393GlyfsTer? | |
| ENST00000450313.5:c.1227_1228dup | ENSP00000408176.1:p.Glu410GlyfsTer? | |
| ENST00000456914.6:c.1143_1144dup | ENSP00000407590.2:p.Glu382GlyfsTer? | |
| ENST00000467459.5:c.560_561dup | ENSP00000435889.1:n.560_561dup | |
| ENST00000475516.5:c.*956_*957dup | ENSP00000433843.1:n.*956_*957dup | |
| ENST00000481571.5:c.*956_*957dup | ENSP00000436597.1:n.*956_*957dup | |
| ENST00000482094.5:n.464_465dup | ||
| ENST00000488731.6:c.228_229dup | ENSP00000432330.1:p.Glu77GlyfsTer? | |
| ENST00000528013.6:c.1185_1186dup | ENSP00000433130.2:p.Glu396GlyfsTer? | |
| ENST00000529892.5:c.218_219dup | ||
| ENST00000529984.5:c.228_229dup | ENSP00000437093.1:p.Glu77GlyfsTer? | |
| ENST00000531105.5:c.116-2079_116-2078dup | ENSP00000431292.1:n.116-2079_116-2078dup | |
| ENST00000533178.5:c.772_773dup | ENSP00000436430.1:n.772_773dup | |
| NM_001048171.1:c.1185_1186dup | NP_001041636.1:p.Glu396GlyfsTer? | |
| NM_001048172.1:c.1146_1147dup | NP_001041637.1:p.Glu383GlyfsTer? | |
| NM_001048173.1:c.1143_1144dup | NP_001041638.1:p.Glu382GlyfsTer? | |
| NM_001048174.1:c.1143_1144dup | NP_001041639.1:p.Glu382GlyfsTer? | |
| NM_001128425.1:c.1227_1228dup , LRG_220t1:c.1227_1228dup | NP_001121897.1:p.Glu410GlyfsTer? | |
| NM_001293190.1:c.1188_1189dup | NP_001280119.1:p.Glu397GlyfsTer? | |
| NM_001293191.1:c.1176_1177dup | NP_001280120.1:p.Glu393GlyfsTer? | |
| NM_001293192.1:c.867_868dup | NP_001280121.1:p.Glu290GlyfsTer? | |
| NM_001293195.1:c.1143_1144dup | NP_001280124.1:p.Glu382GlyfsTer? | |
| NM_001293196.1:c.867_868dup | NP_001280125.1:p.Glu290GlyfsTer? | |
| NM_012222.2:c.1218_1219dup | NP_036354.1:p.Glu407GlyfsTer? | |
| XM_011541497.1:c.1203_1204dup | XP_011539799.1:p.Glu402GlyfsTer? | |
| XM_011541498.1:c.1185_1186dup | XP_011539800.1:p.Glu396GlyfsTer? | |
| XM_011541499.1:c.1185_1186dup | XP_011539801.1:p.Glu396GlyfsTer? | |
| XM_011541500.1:c.1185_1186dup | XP_011539802.1:p.Glu396GlyfsTer? | |
| XM_011541501.1:c.1185_1186dup | XP_011539803.1:p.Glu396GlyfsTer? | |
| XM_011541502.1:c.1185_1186dup | XP_011539804.1:p.Glu396GlyfsTer? | |
| XM_011541503.1:c.1185_1186dup | XP_011539805.1:p.Glu396GlyfsTer? | |
| XM_011541504.1:c.1176_1177dup | XP_011539806.1:p.Glu393GlyfsTer? | |
| XM_011541505.1:c.765_766dup | XP_011539807.1:p.Glu256GlyfsTer? | |
| XM_011541506.1:c.765_766dup | XP_011539808.1:p.Glu256GlyfsTer? | |
| XM_011541507.1:c.756_757dup | XP_011539809.1:p.Glu253GlyfsTer? | |
| XM_011541508.1:c.771_772dup | XP_011539810.1:p.Glu258GlyfsTer? | |
| XR_946658.1:n.1274_1275dup | ||
| NM_001350650.1:c.798_799dup | NP_001337579.1:p.Glu267GlyfsTer? | |
| NM_001350651.1:c.798_799dup | NP_001337580.1:p.Glu267GlyfsTer? | |
| NR_146882.1:n.1401_1402dup | ||
| NR_146883.1:n.1215_1216dup | ||
| XM_011541497.3:c.1203_1204dup | XP_011539799.1:p.Glu402GlyfsTer? | |
| XM_011541500.3:c.1185_1186dup | XP_011539802.1:p.Glu396GlyfsTer? | |
| XM_011541501.2:c.1185_1186dup | XP_011539803.1:p.Glu396GlyfsTer? | |
| XM_011541502.2:c.1185_1186dup | XP_011539804.1:p.Glu396GlyfsTer? | |
| XM_011541503.2:c.1185_1186dup | XP_011539805.1:p.Glu396GlyfsTer? | |
| XM_011541504.2:c.1176_1177dup | XP_011539806.1:p.Glu393GlyfsTer? | |
| XM_011541505.2:c.765_766dup | XP_011539807.1:p.Glu256GlyfsTer? | |
| XM_011541506.2:c.765_766dup | XP_011539808.1:p.Glu256GlyfsTer? | |
| XM_017001331.1:c.1185_1186dup | XP_016856820.1:p.Glu396GlyfsTer? | |
| XM_017001332.1:c.1185_1186dup | XP_016856821.1:p.Glu396GlyfsTer? | |
| XM_017001333.1:c.1185_1186dup | XP_016856822.1:p.Glu396GlyfsTer? | |
| XM_017001334.1:c.1146_1147dup | XP_016856823.1:p.Glu383GlyfsTer? | |
| XM_017001335.1:c.867_868dup | XP_016856824.1:p.Glu290GlyfsTer? | |
| XM_017001336.1:c.798_799dup | XP_016856825.1:p.Glu267GlyfsTer? | |
| XM_017001337.1:c.798_799dup | XP_016856826.1:p.Glu267GlyfsTer? | |
| XM_024447244.1:c.798_799dup | XP_024303012.1:p.Glu267GlyfsTer? | |
| XM_024447245.1:c.798_799dup | XP_024303013.1:p.Glu267GlyfsTer? | |
| XM_024447248.1:c.756_757dup | XP_024303016.1:p.Glu253GlyfsTer? | |
| XM_024447249.1:c.627_628dup | XP_024303017.1:p.Glu210GlyfsTer? | |
| XM_024447250.1:c.627_628dup | XP_024303018.1:p.Glu210GlyfsTer? | |
| XM_024447251.1:c.627_628dup | XP_024303019.1:p.Glu210GlyfsTer? | |
| XR_001737190.1:n.1188_1189dup | ||
| XR_001737192.1:n.1000_1001dup | ||
| XR_002956643.1:n.1180_1181dup | ||
| XR_002956644.1:n.1715_1716dup | ||
| XR_946658.2:n.1288_1289dup | ||
| NM_001048171.2:c.1143_1144dup | NP_001041636.2:p.Glu382GlyfsTer? | |
| NM_001128425.2:c.1227_1228dup MANE Plus Clinical | NP_001121897.1:p.Glu410GlyfsTer? | |
| NM_001048172.2:c.1146_1147dup | NP_001041637.1:p.Glu383GlyfsTer? | |
| NM_001048173.2:c.1143_1144dup | NP_001041638.1:p.Glu382GlyfsTer? | |
| NM_001048174.2:c.1143_1144dup MANE Select | NP_001041639.1:p.Glu382GlyfsTer? | |
| NM_001293190.2:c.1188_1189dup | NP_001280119.1:p.Glu397GlyfsTer? | |
| NM_001293191.2:c.1176_1177dup | NP_001280120.1:p.Glu393GlyfsTer? | |
| NM_001293192.2:c.867_868dup | NP_001280121.1:p.Glu290GlyfsTer? | |
| NM_001293195.2:c.1143_1144dup | NP_001280124.1:p.Glu382GlyfsTer? | |
| NM_001293196.2:c.867_868dup | NP_001280125.1:p.Glu290GlyfsTer? | |
| NM_001350650.2:c.798_799dup | NP_001337579.1:p.Glu267GlyfsTer? | |
| NM_001350651.2:c.798_799dup | NP_001337580.1:p.Glu267GlyfsTer? | |
| NM_012222.3:c.1218_1219dup | NP_036354.1:p.Glu407GlyfsTer? | |
| NR_146882.2:n.1371_1372dup | ||
| NR_146883.2:n.1220_1221dup |