Canonical Allele Identifier: CA1619078419

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269807_31269808delinsCT , CM000668.2:g.31269807_31269808delinsCT	GRCh38
NC_000006.11:g.31237584_31237585delinsCT , CM000668.1:g.31237584_31237585delinsCT	GRCh37
NC_000006.10:g.31345563_31345564delinsCT	NCBI36
NG_029422.2:g.7324_7325delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1015+158_1015+159delinsAG MANE Select	ENSP00000365402.5:n.1015+158_1015+159delinsAG
ENST00000376228.9:c.1015+158_1015+159delinsAG	ENSP00000365402.5:n.1015+158_1015+159delinsAG
ENST00000376237.8:c.*602+158_*602+159delinsAG	ENSP00000365412.4:n.*602+158_*602+159delinsAG
ENST00000383329.7:c.1015+158_1015+159delinsAG	ENSP00000372819.3:n.1015+158_1015+159delinsAG
ENST00000470363.5:n.491_492delinsAG
ENST00000487245.5:n.1374+158_1374+159delinsAG
NM_002117.5:c.1015+158_1015+159delinsAG	NP_002108.4:n.1015+158_1015+159delinsAG
NM_002117.6:c.1015+158_1015+159delinsAG MANE Select	NP_002108.4:n.1015+158_1015+159delinsAG