Canonical Allele Identifier: CA1619079945
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270453G= , CM000668.2:g.31270453G= GRCh38
NC_000006.11:g.31238230G= , CM000668.1:g.31238230G= GRCh37
NC_000006.10:g.31346209G= NCBI36
NG_029422.2:g.6679C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.652C= MANE Select ENSP00000365402.5:p.Leu218=
ENST00000376228.9:c.652C= ENSP00000365402.5:p.Leu218=
ENST00000376237.8:c.*239C= ENSP00000365412.4:n.*239C=
ENST00000383329.7:c.652C= ENSP00000372819.3:p.Leu218=
ENST00000415537.1:c.650C=
ENST00000487245.5:n.1011C=
ENST00000495835.1:n.841C=
NM_002117.5:c.652C= NP_002108.4:p.Leu218=
NM_002117.6:c.652C= MANE Select NP_002108.4:p.Leu218=