Canonical Allele Identifier: CA1619079837
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270377C= , CM000668.2:g.31270377C= GRCh38
NC_000006.11:g.31238154C= , CM000668.1:g.31238154C= GRCh37
NC_000006.10:g.31346133C= NCBI36
NG_029422.2:g.6755G=

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.728G= MANE Select ENSP00000365402.5:p.Arg243=
ENST00000376228.9:c.728G= ENSP00000365402.5:p.Arg243=
ENST00000376237.8:c.*315G= ENSP00000365412.4:n.*315G=
ENST00000383329.7:c.728G= ENSP00000372819.3:p.Arg243=
ENST00000415537.1:c.665-46G=
ENST00000470363.5:n.46G=
ENST00000487245.5:n.1087G=
ENST00000495835.1:n.917G=
NM_002117.5:c.728G= NP_002108.4:p.Arg243=
NM_002117.6:c.728G= MANE Select NP_002108.4:p.Arg243=