Canonical Allele Identifier: CA2677950046

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31269750-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269750_31269751insT , CM000668.2:g.31269750_31269751insT	GRCh38
NC_000006.11:g.31237527_31237528insT , CM000668.1:g.31237527_31237528insT	GRCh37
NC_000006.10:g.31345506_31345507insT	NCBI36
NG_029422.2:g.7381_7382insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1015+215_1015+216insA MANE Select	ENSP00000365402.5:n.1015+215_1015+216insA
ENST00000376228.9:c.1015+215_1015+216insA	ENSP00000365402.5:n.1015+215_1015+216insA
ENST00000376237.8:c.*602+215_*602+216insA	ENSP00000365412.4:n.*602+215_*602+216insA
ENST00000383329.7:c.1016-208_1016-207insA	ENSP00000372819.3:n.1016-208_1016-207insA
ENST00000470363.5:n.548_549insA
ENST00000487245.5:n.1374+215_1374+216insA
NM_002117.5:c.1015+215_1015+216insA	NP_002108.4:n.1015+215_1015+216insA
NM_002117.6:c.1015+215_1015+216insA MANE Select	NP_002108.4:n.1015+215_1015+216insA