Canonical Allele Identifier: CA2770490942

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269886_31269887insTT , CM000668.2:g.31269886_31269887insTT	GRCh38
NC_000006.11:g.31237663_31237664insTT , CM000668.1:g.31237663_31237664insTT	GRCh37
NC_000006.10:g.31345642_31345643insTT	NCBI36
NG_029422.2:g.7245_7246insAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1015+79_1015+80insAA MANE Select	ENSP00000365402.5:n.1015+79_1015+80insAA
ENST00000376228.9:c.1015+79_1015+80insAA	ENSP00000365402.5:n.1015+79_1015+80insAA
ENST00000376237.8:c.*602+79_*602+80insAA	ENSP00000365412.4:n.*602+79_*602+80insAA
ENST00000383329.7:c.1015+79_1015+80insAA	ENSP00000372819.3:n.1015+79_1015+80insAA
ENST00000470363.5:n.412_413insAA
ENST00000487245.5:n.1374+79_1374+80insAA
NM_002117.5:c.1015+79_1015+80insAA	NP_002108.4:n.1015+79_1015+80insAA
NM_002117.6:c.1015+79_1015+80insAA MANE Select	NP_002108.4:n.1015+79_1015+80insAA