Canonical Allele Identifier: CA2770491532

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271278_31271279insGT , CM000668.2:g.31271278_31271279insGT	GRCh38
NC_000006.11:g.31239055_31239056insGT , CM000668.1:g.31239055_31239056insGT	GRCh37
NC_000006.10:g.31347034_31347035insGT	NCBI36
NG_029422.2:g.5853_5854insAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.413_414insAC MANE Select	ENSP00000365402.5:p.Asp138GlufsTer14
ENST00000376228.9:c.413_414insAC	ENSP00000365402.5:p.Asp138GlufsTer14
ENST00000376237.8:c.396_*1insAC	ENSP00000365412.4:n.396_*1insAC
ENST00000383329.7:c.413_414insAC	ENSP00000372819.3:p.Asp138GlufsTer14
ENST00000415537.1:c.411_412insAC
ENST00000484378.1:n.682_683insAC
ENST00000487245.5:n.772_773insAC
ENST00000495835.1:n.602_603insAC
NM_002117.5:c.413_414insAC	NP_002108.4:p.Asp138GlufsTer14
NM_002117.6:c.413_414insAC MANE Select	NP_002108.4:p.Asp138GlufsTer14