Canonical Allele Identifier: CA566689003

Gene: HLA-C

Linked Data

• dbSNP Id: rs1335092784
• gnomAD v2: 6-31239169-C-CA
• gnomAD v3: 6-31271392-C-CA
• gnomAD v4: 6-31271392-C-CA
• MyVariant Identifiers: chr6:g.31239169_31239170insA (hg19) ; chr6:g.31271392_31271393insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271392_31271393insA , CM000668.2:g.31271392_31271393insA	GRCh38
NC_000006.11:g.31239169_31239170insA , CM000668.1:g.31239169_31239170insA	GRCh37
NC_000006.10:g.31347148_31347149insA	NCBI36
NG_029422.2:g.5739_5740insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.344-45_344-44insT MANE Select	ENSP00000365402.5:n.344-45_344-44insT
ENST00000376228.9:c.344-45_344-44insT	ENSP00000365402.5:n.344-45_344-44insT
ENST00000376237.8:c.344-62_344-61insT	ENSP00000365412.4:n.344-62_344-61insT
ENST00000383329.7:c.344-45_344-44insT	ENSP00000372819.3:n.344-45_344-44insT
ENST00000415537.1:c.342-45_342-44insT
ENST00000484378.1:n.568_569insT
ENST00000487245.5:n.658_659insT
ENST00000495835.1:n.533-45_533-44insT
NM_002117.5:c.344-45_344-44insT	NP_002108.4:n.344-45_344-44insT
NM_002117.6:c.344-45_344-44insT MANE Select	NP_002108.4:n.344-45_344-44insT