Canonical Allele Identifier: CA1619078416

Gene: HLA-C

Linked Data

• dbSNP Id: rs1761149257

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269802_31269803del , CM000668.2:g.31269802_31269803del	GRCh38
NC_000006.11:g.31237579_31237580del , CM000668.1:g.31237579_31237580del	GRCh37
NC_000006.10:g.31345558_31345559del	NCBI36
NG_029422.2:g.7329_7330del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1015+163_1015+164del MANE Select	ENSP00000365402.5:n.1015+163_1015+164del
ENST00000376228.9:c.1015+163_1015+164del	ENSP00000365402.5:n.1015+163_1015+164del
ENST00000376237.8:c.*602+163_*602+164del	ENSP00000365412.4:n.*602+163_*602+164del
ENST00000383329.7:c.1015+163_1015+164del	ENSP00000372819.3:n.1015+163_1015+164del
ENST00000470363.5:n.496_497del
ENST00000487245.5:n.1374+163_1374+164del
NM_002117.5:c.1015+163_1015+164del	NP_002108.4:n.1015+163_1015+164del
NM_002117.6:c.1015+163_1015+164del MANE Select	NP_002108.4:n.1015+163_1015+164del