Canonical Allele Identifier: CA566688939

Gene: HLA-C

Linked Data

• dbSNP Id: rs1280754318
• gnomAD v2: 6-31237801-A-AGCC
• gnomAD v4: 6-31270024-A-AGCC
• MyVariant Identifiers: chr6:g.31237801_31237802insGCC (hg19) ; chr6:g.31270024_31270025insGCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31270024_31270025insGCC , CM000668.2:g.31270024_31270025insGCC	GRCh38
NC_000006.11:g.31237801_31237802insGCC , CM000668.1:g.31237801_31237802insGCC	GRCh37
NC_000006.10:g.31345780_31345781insGCC	NCBI36
NG_029422.2:g.7107_7108insGGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.956_957insGGC MANE Select	ENSP00000365402.5:p.Val319_Val320insAla
ENST00000376228.9:c.956_957insGGC	ENSP00000365402.5:p.Val319_Val320insAla
ENST00000376237.8:c.*543_*544insGGC	ENSP00000365412.4:n.*543_*544insGGC
ENST00000383329.7:c.956_957insGGC	ENSP00000372819.3:p.Val319_Val320insAla
ENST00000470363.5:n.274_275insGGC
ENST00000487245.5:n.1315_1316insGGC
NM_002117.5:c.956_957insGGC	NP_002108.4:p.Val319_Val320insAla
NM_002117.6:c.956_957insGGC MANE Select	NP_002108.4:p.Val319_Val320insAla