Canonical Allele Identifier: CA2677951667

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31271577-GCC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271580_31271581del , CM000668.2:g.31271580_31271581del	GRCh38
NC_000006.11:g.31239357_31239358del , CM000668.1:g.31239357_31239358del	GRCh37
NC_000006.10:g.31347336_31347337del	NCBI36
NG_029422.2:g.5553_5554del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.343+20_343+21del MANE Select	ENSP00000365402.5:n.343+20_343+21del
ENST00000376228.9:c.343+20_343+21del	ENSP00000365402.5:n.343+20_343+21del
ENST00000376237.8:c.343+20_343+21del	ENSP00000365412.4:n.343+20_343+21del
ENST00000383329.7:c.343+20_343+21del	ENSP00000372819.3:n.343+20_343+21del
ENST00000415537.1:c.341+20_341+21del
ENST00000484378.1:n.382_383del
ENST00000487245.5:n.472_473del
ENST00000495835.1:n.532+20_532+21del
NM_002117.5:c.343+20_343+21del	NP_002108.4:n.343+20_343+21del
NM_002117.6:c.343+20_343+21del MANE Select	NP_002108.4:n.343+20_343+21del