Canonical Allele Identifier: CA2677951346
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271324_31271325insCAT , CM000668.2:g.31271324_31271325insCAT GRCh38
NC_000006.11:g.31239101_31239102insCAT , CM000668.1:g.31239101_31239102insCAT GRCh37
NC_000006.10:g.31347080_31347081insCAT NCBI36
NG_029422.2:g.5807_5808insATG

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.367_368insATG MANE Select ENSP00000365402.5:p.Ser123delinsTyrAla
ENST00000376228.9:c.367_368insATG ENSP00000365402.5:p.Ser123delinsTyrAla
ENST00000376237.8:c.350_351insATG ENSP00000365412.4:p.Val117_Trp118insCys
ENST00000383329.7:c.367_368insATG ENSP00000372819.3:p.Ser123delinsTyrAla
ENST00000415537.1:c.365_366insATG
ENST00000484378.1:n.636_637insATG
ENST00000487245.5:n.726_727insATG
ENST00000495835.1:n.556_557insATG
NM_002117.5:c.367_368insATG NP_002108.4:p.Ser123delinsTyrAla
NM_002117.6:c.367_368insATG MANE Select NP_002108.4:p.Ser123delinsTyrAla