Linked Data
ClinVar Variation Id:
376012
ClinVar RCV Id:
RCV000437921
dbSNP Id:
rs1057519744
MyVariant Identifiers:
chr5:g.170837546_170837547insTCTG (hg19)
chr5:g.171410542_171410543insTCTG (hg38)
PubMed:
PMID:19657110
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.171410542_171410543insTCTG , CM000667.2:g.171410542_171410543insTCTG | GRCh38 |
| NC_000005.9:g.170837546_170837547insTCTG , CM000667.1:g.170837546_170837547insTCTG | GRCh37 |
| NC_000005.8:g.170770151_170770152insTCTG | NCBI36 |
| NG_016018.1:g.27839_27840insTCTG , LRG_458:g.27839_27840insTCTG |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000296930.10:c.862_863insTCTG MANE Select | ENSP00000296930.5:p.Trp288PhefsTer12 | |
| ENST00000518587.2:n.1056_1057insTCTG | ||
| ENST00000521260.2:n.1240_1241insTCTG | ||
| ENST00000521672.6:c.670_671insTCTG | ENSP00000429485.2:p.Trp224PhefsTer12 | |
| ENST00000676504.1:n.1608_1609insTCTG | ||
| ENST00000676589.1:c.949_950insTCTG | ENSP00000503283.1:p.Trp317PhefsTer12 | |
| ENST00000676613.1:c.*1609_*1610insTCTG | ENSP00000503767.1:n.*1609_*1610insTCTG | |
| ENST00000676625.1:n.3279_3280insTCTG | ||
| ENST00000677297.1:c.349_350insTCTG | ENSP00000504016.1:p.Trp117PhefsTer12 | |
| ENST00000677325.1:c.670_671insTCTG | ENSP00000503781.1:p.Trp224PhefsTer12 | |
| ENST00000677357.1:c.895_896insTCTG | ENSP00000504740.1:p.Trp299PhefsTer12 | |
| ENST00000677467.1:n.2287_2288insTCTG | ||
| ENST00000677600.1:n.2180_2181insTCTG | ||
| ENST00000677672.1:n.2285_2286insTCTG | ||
| ENST00000677682.1:n.2192_2193insTCTG | ||
| ENST00000677741.1:n.2128_2129insTCTG | ||
| ENST00000677904.1:n.1138_1139insTCTG | ||
| ENST00000677907.1:c.583_584insTCTG | ENSP00000504308.1:p.Trp195PhefsTer12 | |
| ENST00000678186.1:n.2332_2333insTCTG | ||
| ENST00000678267.1:c.*1963_*1964insTCTG | ENSP00000504107.1:n.*1963_*1964insTCTG | |
| ENST00000678280.1:c.*847_*848insTCTG | ENSP00000503235.1:n.*847_*848insTCTG | |
| ENST00000678774.1:c.*338_*339insTCTG | ENSP00000503150.1:n.*338_*339insTCTG | |
| ENST00000679190.1:c.*45_*46insTCTG | ENSP00000503408.1:n.*45_*46insTCTG | |
| ENST00000296930.9:c.862_863insTCTG | ENSP00000296930.5:p.Trp288PhefsTer12 | |
| ENST00000351986.10:c.775_776insTCTG | ENSP00000341168.6:p.Trp259PhefsTer12 | |
| ENST00000517671.5:c.862_863insTCTG | ENSP00000428755.1:p.Trp288PhefsTer12 | |
| ENST00000524204.1:n.298_299insTCTG | ||
| NM_002520.6:c.862_863insTCTG , LRG_458t1:c.862_863insTCTG | NP_002511.1:p.Trp288PhefsTer12 | |
| NM_199185.3:c.775_776insTCTG | NP_954654.1:p.Trp259PhefsTer12 | |
| XM_011534564.1:c.670_671insTCTG | XP_011532866.1:p.Trp224PhefsTer12 | |
| NM_001355006.1:c.862_863insTCTG | NP_001341935.1:p.Trp288PhefsTer12 | |
| NM_001355007.1:c.670_671insTCTG | NP_001341936.1:p.Trp224PhefsTer12 | |
| NM_001355010.1:c.481_482insTCTG | NP_001341939.1:p.Trp161PhefsTer12 | |
| NR_149149.1:n.979_980insTCTG | ||
| NM_001355006.2:c.862_863insTCTG | NP_001341935.1:p.Trp288PhefsTer12 | |
| NM_001355007.2:c.670_671insTCTG | NP_001341936.1:p.Trp224PhefsTer12 | |
| NM_001355010.2:c.481_482insTCTG | NP_001341939.1:p.Trp161PhefsTer12 | |
| NM_002520.7:c.862_863insTCTG MANE Select | NP_002511.1:p.Trp288PhefsTer12 | |
| NM_199185.4:c.775_776insTCTG | NP_954654.1:p.Trp259PhefsTer12 | |
| NR_149149.2:n.834_835insTCTG |