Canonical Allele Identifier: CA1619077737
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269364G= , CM000668.2:g.31269364G= GRCh38
NC_000006.11:g.31237141G= , CM000668.1:g.31237141G= GRCh37
NC_000006.10:g.31345120G= NCBI36
NG_029422.2:g.7768C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1070C= MANE Select ENSP00000365402.5:p.Ser357=
ENST00000376228.9:c.1070C= ENSP00000365402.5:p.Ser357=
ENST00000376237.8:c.*657C= ENSP00000365412.4:n.*657C=
ENST00000383329.7:c.1088C= ENSP00000372819.3:p.Ser363=
ENST00000466892.5:n.303C=
ENST00000470363.5:n.828C=
ENST00000487245.5:n.1429C=
NM_002117.5:c.1070C= NP_002108.4:p.Ser357=
NM_002117.6:c.1070C= MANE Select NP_002108.4:p.Ser357=