Canonical Allele Identifier: CA1619077232
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269026T= , CM000668.2:g.31269026T= GRCh38
NC_000006.11:g.31236803T= , CM000668.1:g.31236803T= GRCh37
NC_000006.10:g.31344782T= NCBI36
NG_029422.2:g.8106A=

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.*143A= MANE Select ENSP00000365402.5:n.*143A=
ENST00000376228.9:c.*143A= ENSP00000365402.5:n.*143A=
ENST00000376237.8:c.*831A= ENSP00000365412.4:n.*831A=
ENST00000383329.7:c.*143A= ENSP00000372819.3:n.*143A=
ENST00000466892.5:n.477A=
ENST00000470363.5:n.1002A=
ENST00000487245.5:n.1603A=
NM_002117.5:c.*143A= NP_002108.4:n.*143A=
NM_002117.6:c.*143A= MANE Select NP_002108.4:n.*143A=