Canonical Allele Identifier: CA1619080396
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271189_31271190delinsTG , CM000668.2:g.31271189_31271190delinsTG GRCh38
NC_000006.11:g.31238966_31238967delinsTG , CM000668.1:g.31238966_31238967delinsTG GRCh37
NC_000006.10:g.31346945_31346946delinsTG NCBI36
NG_029422.2:g.5942_5943delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.502_503delinsCA MANE Select ENSP00000365402.5:p.Gln168=
ENST00000376228.9:c.502_503delinsCA ENSP00000365402.5:p.Gln168=
ENST00000376237.8:c.*89_*90delinsCA ENSP00000365412.4:n.*89_*90delinsCA
ENST00000383329.7:c.502_503delinsCA ENSP00000372819.3:p.Gln168=
ENST00000415537.1:c.500_501delinsCA
ENST00000484378.1:n.771_772delinsCA
ENST00000487245.5:n.861_862delinsCA
ENST00000495835.1:n.691_692delinsCA
NM_002117.5:c.502_503delinsCA NP_002108.4:p.Gln168=
NM_002117.6:c.502_503delinsCA MANE Select NP_002108.4:p.Gln168=