Canonical Allele Identifier: CA2677951453

Gene: HLA-C

Linked Data

• dbSNP Id: rs1339870865
• gnomAD v4: 6-31271414-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271418del , CM000668.2:g.31271418del	GRCh38
NC_000006.11:g.31239195del , CM000668.1:g.31239195del	GRCh37
NC_000006.10:g.31347174del	NCBI36
NG_029422.2:g.5717del

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.344-67del MANE Select	ENSP00000365402.5:n.344-67del
ENST00000376228.9:c.344-67del	ENSP00000365402.5:n.344-67del
ENST00000376237.8:c.344-84del	ENSP00000365412.4:n.344-84del
ENST00000383329.7:c.344-67del	ENSP00000372819.3:n.344-67del
ENST00000415537.1:c.342-67del
ENST00000484378.1:n.546del
ENST00000487245.5:n.636del
ENST00000495835.1:n.533-67del
NM_002117.5:c.344-67del	NP_002108.4:n.344-67del
NM_002117.6:c.344-67del MANE Select	NP_002108.4:n.344-67del