Canonical Allele Identifier: CA1619078028
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269518T= , CM000668.2:g.31269518T= GRCh38
NC_000006.11:g.31237295T= , CM000668.1:g.31237295T= GRCh37
NC_000006.10:g.31345274T= NCBI36
NG_029422.2:g.7614A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1023A= MANE Select ENSP00000365402.5:p.Lys341=
ENST00000376228.9:c.1023A= ENSP00000365402.5:p.Lys341=
ENST00000376237.8:c.*610A= ENSP00000365412.4:n.*610A=
ENST00000383329.7:c.1041A= ENSP00000372819.3:p.Lys347=
ENST00000466892.5:n.149A=
ENST00000470363.5:n.781A=
ENST00000487245.5:n.1382A=
NM_002117.5:c.1023A= NP_002108.4:p.Lys341=
NM_002117.6:c.1023A= MANE Select NP_002108.4:p.Lys341=