Canonical Allele Identifier: CA1619080532
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271335G= , CM000668.2:g.31271335G= GRCh38
NC_000006.11:g.31239112G= , CM000668.1:g.31239112G= GRCh37
NC_000006.10:g.31347091G= NCBI36
NG_029422.2:g.5797C=

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.357C= MANE Select ENSP00000365402.5:p.Leu119=
ENST00000376228.9:c.357C= ENSP00000365402.5:p.Leu119=
ENST00000376237.8:c.344-4C= ENSP00000365412.4:n.344-4C=
ENST00000383329.7:c.357C= ENSP00000372819.3:p.Leu119=
ENST00000415537.1:c.355C=
ENST00000484378.1:n.626C=
ENST00000487245.5:n.716C=
ENST00000495835.1:n.546C=
NM_002117.5:c.357C= NP_002108.4:p.Leu119=
NM_002117.6:c.357C= MANE Select NP_002108.4:p.Leu119=