Canonical Allele Identifier: CA1619078036
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269522C= , CM000668.2:g.31269522C= GRCh38
NC_000006.11:g.31237299C= , CM000668.1:g.31237299C= GRCh37
NC_000006.10:g.31345278C= NCBI36
NG_029422.2:g.7610G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1019G= MANE Select ENSP00000365402.5:p.Gly340=
ENST00000376228.9:c.1019G= ENSP00000365402.5:p.Gly340=
ENST00000376237.8:c.*606G= ENSP00000365412.4:n.*606G=
ENST00000383329.7:c.1037G= ENSP00000372819.3:p.Gly346=
ENST00000466892.5:n.145G=
ENST00000470363.5:n.777G=
ENST00000487245.5:n.1378G=
NM_002117.5:c.1019G= NP_002108.4:p.Gly340=
NM_002117.6:c.1019G= MANE Select NP_002108.4:p.Gly340=