Canonical Allele Identifier: CA2677950302

Gene: HLA-C

Linked Data - Sequence & Population

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31270002_31270003insCAT , CM000668.2:g.31270002_31270003insCAT	GRCh38
NC_000006.11:g.31237779_31237780insCAT , CM000668.1:g.31237779_31237780insCAT	GRCh37
NC_000006.10:g.31345758_31345759insCAT	NCBI36
NG_029422.2:g.7129_7130insATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.978_979insATG MANE Select	ENSP00000365402.5:p.Ala326_Val327insMet
ENST00000376228.9:c.978_979insATG	ENSP00000365402.5:p.Ala326_Val327insMet
ENST00000376237.8:c.*565_*566insATG	ENSP00000365412.4:n.*565_*566insATG
ENST00000383329.7:c.978_979insATG	ENSP00000372819.3:p.Ala326_Val327insMet
ENST00000470363.5:n.296_297insATG
ENST00000487245.5:n.1337_1338insATG
NM_002117.5:c.978_979insATG	NP_002108.4:p.Ala326_Val327insMet
NM_002117.6:c.978_979insATG MANE Select	NP_002108.4:p.Ala326_Val327insMet