Canonical Allele Identifier: CA1619079009
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270085T= , CM000668.2:g.31270085T= GRCh38
NC_000006.11:g.31237862T= , CM000668.1:g.31237862T= GRCh37
NC_000006.10:g.31345841T= NCBI36
NG_029422.2:g.7047A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.896A= MANE Select ENSP00000365402.5:p.Glu299=
ENST00000376228.9:c.896A= ENSP00000365402.5:p.Glu299=
ENST00000376237.8:c.*483A= ENSP00000365412.4:n.*483A=
ENST00000383329.7:c.896A= ENSP00000372819.3:p.Glu299=
ENST00000470363.5:n.214A=
ENST00000487245.5:n.1255A=
NM_002117.5:c.896A= NP_002108.4:p.Glu299=
NM_002117.6:c.896A= MANE Select NP_002108.4:p.Glu299=