Canonical Allele Identifier: CA1619080093

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31270694_31270695delinsTC , CM000668.2:g.31270694_31270695delinsTC	GRCh38
NC_000006.11:g.31238471_31238472delinsTC , CM000668.1:g.31238471_31238472delinsTC	GRCh37
NC_000006.10:g.31346450_31346451delinsTC	NCBI36
NG_029422.2:g.6437_6438delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.620-210_620-209delinsGA MANE Select	ENSP00000365402.5:n.620-210_620-209delinsGA
ENST00000376228.9:c.620-210_620-209delinsGA	ENSP00000365402.5:n.620-210_620-209delinsGA
ENST00000376237.8:c.*207-210_*207-209delinsGA	ENSP00000365412.4:n.*207-210_*207-209delinsGA
ENST00000383329.7:c.620-210_620-209delinsGA	ENSP00000372819.3:n.620-210_620-209delinsGA
ENST00000415537.1:c.618-210_618-209delinsGA
ENST00000487245.5:n.979-210_979-209delinsGA
ENST00000495835.1:n.809-210_809-209delinsGA
NM_002117.5:c.620-210_620-209delinsGA	NP_002108.4:n.620-210_620-209delinsGA
NM_002117.6:c.620-210_620-209delinsGA MANE Select	NP_002108.4:n.620-210_620-209delinsGA