Canonical Allele Identifier: CA1619080338
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271129_31271130delinsCA , CM000668.2:g.31271129_31271130delinsCA GRCh38
NC_000006.11:g.31238906_31238907delinsCA , CM000668.1:g.31238906_31238907delinsCA GRCh37
NC_000006.10:g.31346885_31346886delinsCA NCBI36
NG_029422.2:g.6002_6003delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.562_563delinsTG MANE Select ENSP00000365402.5:p.Cys188=
ENST00000376228.9:c.562_563delinsTG ENSP00000365402.5:p.Cys188=
ENST00000376237.8:c.*149_*150delinsTG ENSP00000365412.4:n.*149_*150delinsTG
ENST00000383329.7:c.562_563delinsTG ENSP00000372819.3:p.Cys188=
ENST00000415537.1:c.560_561delinsTG
ENST00000484378.1:n.831_832delinsTG
ENST00000487245.5:n.921_922delinsTG
ENST00000495835.1:n.751_752delinsTG
NM_002117.5:c.562_563delinsTG NP_002108.4:p.Cys188=
NM_002117.6:c.562_563delinsTG MANE Select NP_002108.4:p.Cys188=