Canonical Allele Identifier: CA2677951396

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31271373-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271373_31271374insT , CM000668.2:g.31271373_31271374insT	GRCh38
NC_000006.11:g.31239150_31239151insT , CM000668.1:g.31239150_31239151insT	GRCh37
NC_000006.10:g.31347129_31347130insT	NCBI36
NG_029422.2:g.5758_5759insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.344-26_344-25insA MANE Select	ENSP00000365402.5:n.344-26_344-25insA
ENST00000376228.9:c.344-26_344-25insA	ENSP00000365402.5:n.344-26_344-25insA
ENST00000376237.8:c.344-43_344-42insA	ENSP00000365412.4:n.344-43_344-42insA
ENST00000383329.7:c.344-26_344-25insA	ENSP00000372819.3:n.344-26_344-25insA
ENST00000415537.1:c.342-26_342-25insA
ENST00000484378.1:n.587_588insA
ENST00000487245.5:n.677_678insA
ENST00000495835.1:n.533-26_533-25insA
NM_002117.5:c.344-26_344-25insA	NP_002108.4:n.344-26_344-25insA
NM_002117.6:c.344-26_344-25insA MANE Select	NP_002108.4:n.344-26_344-25insA