Canonical Allele Identifier: CA1619080298
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271091C= , CM000668.2:g.31271091C= GRCh38
NC_000006.11:g.31238868C= , CM000668.1:g.31238868C= GRCh37
NC_000006.10:g.31346847C= NCBI36
NG_029422.2:g.6041G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.601G= MANE Select ENSP00000365402.5:p.Glu201=
ENST00000376228.9:c.601G= ENSP00000365402.5:p.Glu201=
ENST00000376237.8:c.*188G= ENSP00000365412.4:n.*188G=
ENST00000383329.7:c.601G= ENSP00000372819.3:p.Glu201=
ENST00000415537.1:c.599G=
ENST00000487245.5:n.960G=
ENST00000495835.1:n.790G=
NM_002117.5:c.601G= NP_002108.4:p.Glu201=
NM_002117.6:c.601G= MANE Select NP_002108.4:p.Glu201=