Canonical Allele Identifier: CA566688995

Gene: HLA-C

Linked Data

• gnomAD v2: 6-31239160-AGCCCC-A
• gnomAD v4: 6-31271383-AGCCCC-A
• MyVariant Identifiers: chr6:g.31239161_31239165del (hg19) ; chr6:g.31271384_31271388del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271395_31271399del , CM000668.2:g.31271395_31271399del	GRCh38
NC_000006.11:g.31239172_31239176del , CM000668.1:g.31239172_31239176del	GRCh37
NC_000006.10:g.31347151_31347155del	NCBI36
NG_029422.2:g.5744_5748del

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.344-40_344-36del MANE Select	ENSP00000365402.5:n.344-40_344-36del
ENST00000376228.9:c.344-40_344-36del	ENSP00000365402.5:n.344-40_344-36del
ENST00000376237.8:c.344-57_344-53del	ENSP00000365412.4:n.344-57_344-53del
ENST00000383329.7:c.344-40_344-36del	ENSP00000372819.3:n.344-40_344-36del
ENST00000415537.1:c.342-40_342-36del
ENST00000484378.1:n.573_577del
ENST00000487245.5:n.663_667del
ENST00000495835.1:n.533-40_533-36del
NM_002117.5:c.344-40_344-36del	NP_002108.4:n.344-40_344-36del
NM_002117.6:c.344-40_344-36del MANE Select	NP_002108.4:n.344-40_344-36del