Canonical Allele Identifier: CA566689006

Gene: HLA-C

Linked Data

• gnomAD v2: 6-31239172-C-CATT
• gnomAD v4: 6-31271395-C-CATT
• MyVariant Identifiers: chr6:g.31239172_31239173insATT (hg19) ; chr6:g.31271395_31271396insATT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271395_31271396insATT , CM000668.2:g.31271395_31271396insATT	GRCh38
NC_000006.11:g.31239172_31239173insATT , CM000668.1:g.31239172_31239173insATT	GRCh37
NC_000006.10:g.31347151_31347152insATT	NCBI36
NG_029422.2:g.5736_5737insAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.344-48_344-47insAAT MANE Select	ENSP00000365402.5:n.344-48_344-47insAAT
ENST00000376228.9:c.344-48_344-47insAAT	ENSP00000365402.5:n.344-48_344-47insAAT
ENST00000376237.8:c.344-65_344-64insAAT	ENSP00000365412.4:n.344-65_344-64insAAT
ENST00000383329.7:c.344-48_344-47insAAT	ENSP00000372819.3:n.344-48_344-47insAAT
ENST00000415537.1:c.342-48_342-47insAAT
ENST00000484378.1:n.565_566insAAT
ENST00000487245.5:n.655_656insAAT
ENST00000495835.1:n.533-48_533-47insAAT
NM_002117.5:c.344-48_344-47insAAT	NP_002108.4:n.344-48_344-47insAAT
NM_002117.6:c.344-48_344-47insAAT MANE Select	NP_002108.4:n.344-48_344-47insAAT