Canonical Allele Identifier: CA2677951673

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31271581-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271581_31271582insT , CM000668.2:g.31271581_31271582insT	GRCh38
NC_000006.11:g.31239358_31239359insT , CM000668.1:g.31239358_31239359insT	GRCh37
NC_000006.10:g.31347337_31347338insT	NCBI36
NG_029422.2:g.5550_5551insA

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.343+17_343+18insA MANE Select	ENSP00000365402.5:n.343+17_343+18insA
ENST00000376228.9:c.343+17_343+18insA	ENSP00000365402.5:n.343+17_343+18insA
ENST00000376237.8:c.343+17_343+18insA	ENSP00000365412.4:n.343+17_343+18insA
ENST00000383329.7:c.343+17_343+18insA	ENSP00000372819.3:n.343+17_343+18insA
ENST00000415537.1:c.341+17_341+18insA
ENST00000484378.1:n.379_380insA
ENST00000487245.5:n.469_470insA
ENST00000495835.1:n.532+17_532+18insA
NM_002117.5:c.343+17_343+18insA	NP_002108.4:n.343+17_343+18insA
NM_002117.6:c.343+17_343+18insA MANE Select	NP_002108.4:n.343+17_343+18insA