Canonical Allele Identifier: CA2677951707
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271635del , CM000668.2:g.31271635del GRCh38
NC_000006.11:g.31239412del , CM000668.1:g.31239412del GRCh37
NC_000006.10:g.31347391del NCBI36
NG_029422.2:g.5497del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.307del MANE Select ENSP00000365402.5:p.Arg103GlyfsTer?
ENST00000376228.9:c.307del ENSP00000365402.5:p.Arg103GlyfsTer?
ENST00000376237.8:c.307del ENSP00000365412.4:p.Arg103GlyfsTer?
ENST00000383329.7:c.307del ENSP00000372819.3:p.Arg103GlyfsTer?
ENST00000415537.1:c.305del
ENST00000484378.1:n.326del
ENST00000487245.5:n.416del
ENST00000495835.1:n.496del
NM_002117.5:c.307del NP_002108.4:p.Arg103GlyfsTer?
NM_002117.6:c.307del MANE Select NP_002108.4:p.Arg103GlyfsTer?