Canonical Allele Identifier: CA1619080269
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271053C= , CM000668.2:g.31271053C= GRCh38
NC_000006.11:g.31238830C= , CM000668.1:g.31238830C= GRCh37
NC_000006.10:g.31346809C= NCBI36
NG_029422.2:g.6079G=

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.619+20G= MANE Select ENSP00000365402.5:n.619+20G=
ENST00000376228.9:c.619+20G= ENSP00000365402.5:n.619+20G=
ENST00000376237.8:c.*206+20G= ENSP00000365412.4:n.*206+20G=
ENST00000383329.7:c.619+20G= ENSP00000372819.3:n.619+20G=
ENST00000415537.1:c.617+20G=
ENST00000487245.5:n.978+20G=
ENST00000495835.1:n.808+20G=
NM_002117.5:c.619+20G= NP_002108.4:n.619+20G=
NM_002117.6:c.619+20G= MANE Select NP_002108.4:n.619+20G=