Canonical Allele Identifier: CA3710834

Gene: HLA-C

Linked Data

• dbSNP Id: rs761717498
• ExAC: 6:31239167 C / CA
• gnomAD v2: 6-31239167-C-CA
• gnomAD v4: 6-31271390-C-CA
• MyVariant Identifiers: chr6:g.31239167_31239168insA (hg19) ; chr6:g.31271390_31271391insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271390_31271391insA , CM000668.2:g.31271390_31271391insA	GRCh38
NC_000006.11:g.31239167_31239168insA , CM000668.1:g.31239167_31239168insA	GRCh37
NC_000006.10:g.31347146_31347147insA	NCBI36
NG_029422.2:g.5741_5742insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.344-43_344-42insT MANE Select	ENSP00000365402.5:n.344-43_344-42insT
ENST00000376228.9:c.344-43_344-42insT	ENSP00000365402.5:n.344-43_344-42insT
ENST00000376237.8:c.344-60_344-59insT	ENSP00000365412.4:n.344-60_344-59insT
ENST00000383329.7:c.344-43_344-42insT	ENSP00000372819.3:n.344-43_344-42insT
ENST00000415537.1:c.342-43_342-42insT
ENST00000484378.1:n.570_571insT
ENST00000487245.5:n.660_661insT
ENST00000495835.1:n.533-43_533-42insT
NM_002117.5:c.344-43_344-42insT	NP_002108.4:n.344-43_344-42insT
NM_002117.6:c.344-43_344-42insT MANE Select	NP_002108.4:n.344-43_344-42insT