Linked Data
ClinVar Variation Id:
476870
dbSNP Id:
rs377006678
ExAC:
11:95657103 T / A
gnomAD v2:
11-95657103-T-A
gnomAD v3:
11-95923939-T-A
gnomAD v4:
11-95923939-T-A
MyVariant Identifiers:
chr11:g.95657103T>A (hg19)
chr11:g.95657103_95657110delinsACGAGCTC (hg19)
chr11:g.95923939T>A (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.95923939T>A , CM000673.2:g.95923939T>A | GRCh38 |
| NC_000011.9:g.95657103T>A , CM000673.1:g.95657103T>A | GRCh37 |
| NC_000011.8:g.95296751T>A | NCBI36 |
| NG_008333.1:g.5269A>T , LRG_257:g.5269A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000346299.10:c.16A>T MANE Select | ENSP00000345752.6:p.Ser6Cys | |
| ENST00000393223.8:c.-293A>T | ENSP00000376915.3:n.-293A>T | |
| ENST00000481642.6:c.-429A>T | ENSP00000502505.1:n.-429A>T | |
| ENST00000674950.1:c.16A>T | ENSP00000502425.1:p.Ser6Cys | |
| ENST00000674974.1:c.16A>T | ENSP00000502337.1:p.Ser6Cys | |
| ENST00000674989.1:c.-269A>T | ENSP00000502829.1:n.-269A>T | |
| ENST00000675022.1:c.16A>T | ENSP00000502722.1:p.Ser6Cys | |
| ENST00000675024.1:n.169A>T | ||
| ENST00000675030.1:c.16A>T | ENSP00000502386.1:p.Ser6Cys | |
| ENST00000675174.1:c.-322A>T | ENSP00000502032.1:n.-322A>T | |
| ENST00000675320.1:c.16A>T | ENSP00000502076.1:p.Ser6Cys | |
| ENST00000675362.1:c.-366A>T | ENSP00000501989.1:n.-366A>T | |
| ENST00000675489.1:c.-468A>T | ENSP00000501702.1:n.-468A>T | |
| ENST00000675495.1:n.193A>T | ||
| ENST00000675652.1:c.-166A>T | ENSP00000502694.1:n.-166A>T | |
| ENST00000675767.1:n.163A>T | ||
| ENST00000675848.1:c.-565A>T | ENSP00000502057.1:n.-565A>T | |
| ENST00000675896.1:c.16A>T | ENSP00000502487.1:p.Ser6Cys | |
| ENST00000675910.1:c.16A>T | ENSP00000502622.1:p.Ser6Cys | |
| ENST00000675922.1:c.16A>T | ENSP00000502168.1:p.Ser6Cys | |
| ENST00000676027.1:c.-638A>T | ENSP00000502405.1:n.-638A>T | |
| ENST00000676146.1:c.16A>T | ENSP00000502583.1:p.Ser6Cys | |
| ENST00000676177.1:c.16A>T | ENSP00000501635.1:p.Ser6Cys | |
| ENST00000676261.1:c.-395A>T | ENSP00000501675.1:n.-395A>T | |
| ENST00000676268.1:c.16A>T | ENSP00000502444.1:p.Ser6Cys | |
| ENST00000676272.1:c.-95A>T | ENSP00000501601.1:n.-95A>T | |
| ENST00000676388.1:c.16A>T | ENSP00000501866.1:p.Ser6Cys | |
| ENST00000676432.1:n.162A>T | ||
| ENST00000346299.9:c.16A>T | ENSP00000345752.5:p.Ser6Cys | |
| ENST00000352297.11:c.-272A>T | ENSP00000343737.7:n.-272A>T | |
| ENST00000393223.7:c.-201A>T | ENSP00000376915.3:n.-201A>T | |
| ENST00000409459.5:c.-345A>T | ENSP00000386882.1:n.-345A>T | |
| ENST00000470011.5:n.252A>T | ||
| ENST00000481642.5:n.169A>T | ||
| NM_001243571.1:c.-468A>T | NP_001230500.1:n.-468A>T | |
| NM_016156.5:c.16A>T , LRG_257t1:c.16A>T | NP_057240.3:p.Ser6Cys | |
| NM_201278.2:c.-395A>T | NP_958435.1:n.-395A>T | |
| NM_201281.2:c.-272A>T | NP_958438.1:n.-272A>T | |
| XM_005274375.1:c.-324A>T | XP_005274432.1:n.-324A>T | |
| XM_006718934.1:c.-345A>T | XP_006718997.1:n.-345A>T | |
| XM_006718936.2:c.-274A>T | XP_006718999.1:n.-274A>T | |
| XM_011543058.1:c.-354A>T | XP_011541360.1:n.-354A>T | |
| XM_005274375.3:c.-324A>T | XP_005274432.1:n.-324A>T | |
| NM_001243571.2:c.-468A>T | NP_001230500.1:n.-468A>T | |
| NM_016156.6:c.16A>T MANE Select | NP_057240.3:p.Ser6Cys | |
| NM_201278.3:c.-395A>T | NP_958435.1:n.-395A>T | |
| NM_201281.3:c.-272A>T | NP_958438.1:n.-272A>T |