Linked Data
ClinVar Variation Id:
143587
ClinVar RCV Id:
RCV000133125
dbSNP Id:
rs267608483
PubMed:
PMID:11738864
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154031357_154031358del , CM000685.2:g.154031357_154031358del | GRCh38 |
| NC_000023.10:g.153296808_153296809del , CM000685.1:g.153296808_153296809del | GRCh37 |
| NC_000023.9:g.152950002_152950003del | NCBI36 |
| NG_007107.2:g.110770_110771del | |
| NG_007107.3:g.110746_110747del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000303391.11:c.470_471del MANE Plus Clinical | ENSP00000301948.6:p.Phe157TyrfsTer17 | |
| ENST00000453960.7:c.506_507del MANE Select | ENSP00000395535.2:p.Phe169TyrfsTer17 | |
| ENST00000637917.1:c.65+38_65+39del | ||
| ENST00000303391.10:c.470_471del | ENSP00000301948.6:p.Phe157TyrfsTer17 | |
| ENST00000407218.5:c.468+38_468+39del | ENSP00000384865.2:n.468+38_468+39del | |
| ENST00000453960.6:c.506_507del | ENSP00000395535.2:p.Phe169TyrfsTer17 | |
| ENST00000486506.5:n.2818_2819del | ||
| ENST00000611468.1:c.458_459del | ENSP00000479736.1:p.Phe153TyrfsTer? | |
| ENST00000619732.4:c.470_471del | ENSP00000480973.1:p.Phe157TyrfsTer17 | |
| ENST00000622433.4:c.458_459del | ENSP00000484470.1:p.Phe153TyrfsTer17 | |
| ENST00000628176.2:c.432+38_432+39del | ENSP00000486978.1:n.432+38_432+39del | |
| NM_001110792.1:c.506_507del | NP_001104262.1:p.Phe169TyrfsTer17 | |
| NM_001316337.1:c.191_192del | NP_001303266.1:p.Phe64TyrfsTer17 | |
| NM_004992.3:c.470_471del | NP_004983.1:p.Phe157TyrfsTer17 | |
| XM_005274681.3:c.470_471del | XP_005274738.1:p.Phe157TyrfsTer17 | |
| XM_005274682.3:c.191_192del | XP_005274739.1:p.Phe64TyrfsTer17 | |
| XM_005274683.3:c.191_192del | XP_005274740.1:p.Phe64TyrfsTer17 | |
| XM_006724819.2:c.-129+38_-129+39del | XP_006724882.1:n.-129+38_-129+39del | |
| XM_011531166.1:c.191_192del | XP_011529468.1:p.Phe64TyrfsTer17 | |
| XM_006724819.3:c.-129+38_-129+39del | XP_006724882.1:n.-129+38_-129+39del | |
| XM_011531166.2:c.191_192del | XP_011529468.1:p.Phe64TyrfsTer17 | |
| XM_024452383.1:c.191_192del | XP_024308151.1:p.Phe64TyrfsTer17 | |
| XM_024452384.1:c.191_192del | XP_024308152.1:p.Phe64TyrfsTer17 | |
| NM_001110792.2:c.506_507del MANE Select | NP_001104262.1:p.Phe169TyrfsTer17 | |
| NM_001316337.2:c.191_192del | NP_001303266.1:p.Phe64TyrfsTer17 | |
| NM_001369391.2:c.191_192del | NP_001356320.1:p.Phe64TyrfsTer17 | |
| NM_001369392.2:c.191_192del | NP_001356321.1:p.Phe64TyrfsTer17 | |
| NM_001369393.2:c.191_192del | NP_001356322.1:p.Phe64TyrfsTer17 | |
| NM_001369394.1:c.191_192del | NP_001356323.1:p.Phe64TyrfsTer17 | |
| NM_001369394.2:c.191_192del | NP_001356323.1:p.Phe64TyrfsTer17 | |
| NM_001386137.1:c.-129+38_-129+39del | NP_001373066.1:n.-129+38_-129+39del | |
| NM_001386138.1:c.-129+38_-129+39del | NP_001373067.1:n.-129+38_-129+39del | |
| NM_001386139.1:c.-129+38_-129+39del | NP_001373068.1:n.-129+38_-129+39del | |
| NM_004992.4:c.470_471del MANE Plus Clinical | NP_004983.1:p.Phe157TyrfsTer17 |