Canonical Allele Identifier: CA1619079272

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31270189_31270198delinsACCCCCCATT , CM000668.2:g.31270189_31270198delinsACCCCCCATT	GRCh38
NC_000006.11:g.31237966_31237975delinsACCCCCCATT , CM000668.1:g.31237966_31237975delinsACCCCCCATT	GRCh37
NC_000006.10:g.31345945_31345954delinsACCCCCCATT	NCBI36
NG_029422.2:g.6934_6943delinsAATGGGGGGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.895+12_895+21delinsAATGGGGGGT MANE Select	ENSP00000365402.5:n.895+12_895+21delinsAATGGGGGGT
ENST00000376228.9:c.895+12_895+21delinsAATGGGGGGT	ENSP00000365402.5:n.895+12_895+21delinsAATGGGGGGT
ENST00000376237.8:c.*482+12_*482+21delinsAATGGGGGGT	ENSP00000365412.4:n.*482+12_*482+21delinsAATGGGGGGT
ENST00000383329.7:c.895+12_895+21delinsAATGGGGGGT	ENSP00000372819.3:n.895+12_895+21delinsAATGGGGGGT
ENST00000470363.5:n.213+12_213+21delinsAATGGGGGGT
ENST00000487245.5:n.1254+12_1254+21delinsAATGGGGGGT
NM_002117.5:c.895+12_895+21delinsAATGGGGGGT	NP_002108.4:n.895+12_895+21delinsAATGGGGGGT
NM_002117.6:c.895+12_895+21delinsAATGGGGGGT MANE Select	NP_002108.4:n.895+12_895+21delinsAATGGGGGGT