Canonical Allele Identifier: CA1087427780

Gene: HLA-C

Linked Data

• gnomAD v3: 6-31271501-T-TCAG
• gnomAD v4: 6-31271501-T-TCAG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271501_31271502insCAG , CM000668.2:g.31271501_31271502insCAG	GRCh38
NC_000006.11:g.31239278_31239279insCAG , CM000668.1:g.31239278_31239279insCAG	GRCh37
NC_000006.10:g.31347257_31347258insCAG	NCBI36
NG_029422.2:g.5630_5631insCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.343+97_343+98insCTG MANE Select	ENSP00000365402.5:n.343+97_343+98insCTG
ENST00000376228.9:c.343+97_343+98insCTG	ENSP00000365402.5:n.343+97_343+98insCTG
ENST00000376237.8:c.343+97_343+98insCTG	ENSP00000365412.4:n.343+97_343+98insCTG
ENST00000383329.7:c.343+97_343+98insCTG	ENSP00000372819.3:n.343+97_343+98insCTG
ENST00000415537.1:c.341+97_341+98insCTG
ENST00000484378.1:n.459_460insCTG
ENST00000487245.5:n.549_550insCTG
ENST00000495835.1:n.532+97_532+98insCTG
NM_002117.5:c.343+97_343+98insCTG	NP_002108.4:n.343+97_343+98insCTG
NM_002117.6:c.343+97_343+98insCTG MANE Select	NP_002108.4:n.343+97_343+98insCTG