Canonical Allele Identifier: CA2832547562

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31270190_31270191insA , CM000668.2:g.31270190_31270191insA	GRCh38
NC_000006.11:g.31237967_31237968insA , CM000668.1:g.31237967_31237968insA	GRCh37
NC_000006.10:g.31345946_31345947insA	NCBI36
NG_029422.2:g.6941_6942insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.895+19_895+20insT MANE Select	ENSP00000365402.5:n.895+19_895+20insT
ENST00000376228.9:c.895+19_895+20insT	ENSP00000365402.5:n.895+19_895+20insT
ENST00000376237.8:c.*482+19_*482+20insT	ENSP00000365412.4:n.*482+19_*482+20insT
ENST00000383329.7:c.895+19_895+20insT	ENSP00000372819.3:n.895+19_895+20insT
ENST00000470363.5:n.213+19_213+20insT
ENST00000487245.5:n.1254+19_1254+20insT
NM_002117.5:c.895+19_895+20insT	NP_002108.4:n.895+19_895+20insT
NM_002117.6:c.895+19_895+20insT MANE Select	NP_002108.4:n.895+19_895+20insT