Canonical Allele Identifier: CA136865794

Gene: HLA-C

Linked Data

• dbSNP Id: rs867627342
• MyVariant Identifiers: chr6:g.31238142_31238147del (hg19) ; chr6:g.31270365_31270370del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31270365_31270370del , CM000668.2:g.31270365_31270370del	GRCh38
NC_000006.11:g.31238142_31238147del , CM000668.1:g.31238142_31238147del	GRCh37
NC_000006.10:g.31346121_31346126del	NCBI36
NG_029422.2:g.6762_6767del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.735_740del MANE Select	ENSP00000365402.5:p.Glu246_Asp247del
ENST00000376228.9:c.735_740del	ENSP00000365402.5:p.Glu246_Asp247del
ENST00000376237.8:c.*322_*327del	ENSP00000365412.4:n.*322_*327del
ENST00000383329.7:c.735_740del	ENSP00000372819.3:p.Glu246_Asp247del
ENST00000415537.1:c.665-39_665-34del
ENST00000470363.5:n.53_58del
ENST00000487245.5:n.1094_1099del
ENST00000495835.1:n.924_929del
NM_002117.5:c.735_740del	NP_002108.4:p.Glu246_Asp247del
NM_002117.6:c.735_740del MANE Select	NP_002108.4:p.Glu246_Asp247del