Canonical Allele Identifier: CA1619078598

Gene: HLA-C

Linked Data

• dbSNP Id: rs1761159714

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269960_31269961insAC , CM000668.2:g.31269960_31269961insAC	GRCh38
NC_000006.11:g.31237737_31237738insAC , CM000668.1:g.31237737_31237738insAC	GRCh37
NC_000006.10:g.31345716_31345717insAC	NCBI36
NG_029422.2:g.7172_7173insTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.1015+6_1015+7insTG MANE Select	ENSP00000365402.5:n.1015+6_1015+7insTG
ENST00000376228.9:c.1015+6_1015+7insTG	ENSP00000365402.5:n.1015+6_1015+7insTG
ENST00000376237.8:c.*602+6_*602+7insTG	ENSP00000365412.4:n.*602+6_*602+7insTG
ENST00000383329.7:c.1015+6_1015+7insTG	ENSP00000372819.3:n.1015+6_1015+7insTG
ENST00000470363.5:n.339_340insTG
ENST00000487245.5:n.1374+6_1374+7insTG
NM_002117.5:c.1015+6_1015+7insTG	NP_002108.4:n.1015+6_1015+7insTG
NM_002117.6:c.1015+6_1015+7insTG MANE Select	NP_002108.4:n.1015+6_1015+7insTG