Canonical Allele Identifier: CA1619080593
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271394G= , CM000668.2:g.31271394G= GRCh38
NC_000006.11:g.31239171G= , CM000668.1:g.31239171G= GRCh37
NC_000006.10:g.31347150G= NCBI36
NG_029422.2:g.5738C=

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.344-46C= MANE Select ENSP00000365402.5:n.344-46C=
ENST00000376228.9:c.344-46C= ENSP00000365402.5:n.344-46C=
ENST00000376237.8:c.344-63C= ENSP00000365412.4:n.344-63C=
ENST00000383329.7:c.344-46C= ENSP00000372819.3:n.344-46C=
ENST00000415537.1:c.342-46C=
ENST00000484378.1:n.567C=
ENST00000487245.5:n.657C=
ENST00000495835.1:n.533-46C=
NM_002117.5:c.344-46C= NP_002108.4:n.344-46C=
NM_002117.6:c.344-46C= MANE Select NP_002108.4:n.344-46C=