Canonical Allele Identifier: CA1619080696

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271556_31271559delinsTGGG , CM000668.2:g.31271556_31271559delinsTGGG	GRCh38
NC_000006.11:g.31239333_31239336delinsTGGG , CM000668.1:g.31239333_31239336delinsTGGG	GRCh37
NC_000006.10:g.31347312_31347315delinsTGGG	NCBI36
NG_029422.2:g.5573_5576delinsCCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.343+40_343+43delinsCCCA MANE Select	ENSP00000365402.5:n.343+40_343+43delinsCCCA
ENST00000376228.9:c.343+40_343+43delinsCCCA	ENSP00000365402.5:n.343+40_343+43delinsCCCA
ENST00000376237.8:c.343+40_343+43delinsCCCA	ENSP00000365412.4:n.343+40_343+43delinsCCCA
ENST00000383329.7:c.343+40_343+43delinsCCCA	ENSP00000372819.3:n.343+40_343+43delinsCCCA
ENST00000415537.1:c.341+40_341+43delinsCCCA
ENST00000484378.1:n.402_405delinsCCCA
ENST00000487245.5:n.492_495delinsCCCA
ENST00000495835.1:n.532+40_532+43delinsCCCA
NM_002117.5:c.343+40_343+43delinsCCCA	NP_002108.4:n.343+40_343+43delinsCCCA
NM_002117.6:c.343+40_343+43delinsCCCA MANE Select	NP_002108.4:n.343+40_343+43delinsCCCA