Canonical Allele Identifier: CA1619079959
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270481G= , CM000668.2:g.31270481G= GRCh38
NC_000006.11:g.31238258G= , CM000668.1:g.31238258G= GRCh37
NC_000006.10:g.31346237G= NCBI36
NG_029422.2:g.6651C=

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.624C= MANE Select ENSP00000365402.5:p.Pro208=
ENST00000376228.9:c.624C= ENSP00000365402.5:p.Pro208=
ENST00000376237.8:c.*211C= ENSP00000365412.4:n.*211C=
ENST00000383329.7:c.624C= ENSP00000372819.3:p.Pro208=
ENST00000415537.1:c.622C=
ENST00000487245.5:n.983C=
ENST00000495835.1:n.813C=
NM_002117.5:c.624C= NP_002108.4:p.Pro208=
NM_002117.6:c.624C= MANE Select NP_002108.4:p.Pro208=