Canonical Allele Identifier: CA2677950210

Gene: HLA-C

Linked Data - Sequence & Population

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269907_31269908del , CM000668.2:g.31269907_31269908del	GRCh38
NC_000006.11:g.31237684_31237685del , CM000668.1:g.31237684_31237685del	GRCh37
NC_000006.10:g.31345663_31345664del	NCBI36
NG_029422.2:g.7226_7227del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1015+60_1015+61del MANE Select	ENSP00000365402.5:n.1015+60_1015+61del
ENST00000376228.9:c.1015+60_1015+61del	ENSP00000365402.5:n.1015+60_1015+61del
ENST00000376237.8:c.*602+60_*602+61del	ENSP00000365412.4:n.*602+60_*602+61del
ENST00000383329.7:c.1015+60_1015+61del	ENSP00000372819.3:n.1015+60_1015+61del
ENST00000470363.5:n.393_394del
ENST00000487245.5:n.1374+60_1374+61del
NM_002117.5:c.1015+60_1015+61del	NP_002108.4:n.1015+60_1015+61del
NM_002117.6:c.1015+60_1015+61del MANE Select	NP_002108.4:n.1015+60_1015+61del