Canonical Allele Identifier: CA1087427792

Gene: HLA-C

Linked Data

• gnomAD v3: 6-31271504-G-GGA
• gnomAD v4: 6-31271504-G-GGA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271505_31271506insAG , CM000668.2:g.31271505_31271506insAG	GRCh38
NC_000006.11:g.31239282_31239283insAG , CM000668.1:g.31239282_31239283insAG	GRCh37
NC_000006.10:g.31347261_31347262insAG	NCBI36
NG_029422.2:g.5627_5628insTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.343+94_343+95insTC MANE Select	ENSP00000365402.5:n.343+94_343+95insTC
ENST00000376228.9:c.343+94_343+95insTC	ENSP00000365402.5:n.343+94_343+95insTC
ENST00000376237.8:c.343+94_343+95insTC	ENSP00000365412.4:n.343+94_343+95insTC
ENST00000383329.7:c.343+94_343+95insTC	ENSP00000372819.3:n.343+94_343+95insTC
ENST00000415537.1:c.341+94_341+95insTC
ENST00000484378.1:n.456_457insTC
ENST00000487245.5:n.546_547insTC
ENST00000495835.1:n.532+94_532+95insTC
NM_002117.5:c.343+94_343+95insTC	NP_002108.4:n.343+94_343+95insTC
NM_002117.6:c.343+94_343+95insTC MANE Select	NP_002108.4:n.343+94_343+95insTC