Canonical Allele Identifier: CA2677950190

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31269871-GCTTCCA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269872_31269877del , CM000668.2:g.31269872_31269877del	GRCh38
NC_000006.11:g.31237649_31237654del , CM000668.1:g.31237649_31237654del	GRCh37
NC_000006.10:g.31345628_31345633del	NCBI36
NG_029422.2:g.7255_7260del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1015+89_1015+94del MANE Select	ENSP00000365402.5:n.1015+89_1015+94del
ENST00000376228.9:c.1015+89_1015+94del	ENSP00000365402.5:n.1015+89_1015+94del
ENST00000376237.8:c.*602+89_*602+94del	ENSP00000365412.4:n.*602+89_*602+94del
ENST00000383329.7:c.1015+89_1015+94del	ENSP00000372819.3:n.1015+89_1015+94del
ENST00000470363.5:n.422_427del
ENST00000487245.5:n.1374+89_1374+94del
NM_002117.5:c.1015+89_1015+94del	NP_002108.4:n.1015+89_1015+94del
NM_002117.6:c.1015+89_1015+94del MANE Select	NP_002108.4:n.1015+89_1015+94del