Canonical Allele Identifier: CA1619080256
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271030A= , CM000668.2:g.31271030A= GRCh38
NC_000006.11:g.31238807A= , CM000668.1:g.31238807A= GRCh37
NC_000006.10:g.31346786A= NCBI36
NG_029422.2:g.6102T=

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.619+43T= MANE Select ENSP00000365402.5:n.619+43T=
ENST00000376228.9:c.619+43T= ENSP00000365402.5:n.619+43T=
ENST00000376237.8:c.*206+43T= ENSP00000365412.4:n.*206+43T=
ENST00000383329.7:c.619+43T= ENSP00000372819.3:n.619+43T=
ENST00000415537.1:c.617+43T=
ENST00000487245.5:n.978+43T=
ENST00000495835.1:n.808+43T=
NM_002117.5:c.619+43T= NP_002108.4:n.619+43T=
NM_002117.6:c.619+43T= MANE Select NP_002108.4:n.619+43T=