Canonical Allele Identifier: CA1087425162

Gene: HLA-C

Linked Data

• dbSNP Id: rs1761262689
• gnomAD v3: 6-31270829-TCAAAGGA-T
• gnomAD v4: 6-31270829-TCAAAGGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31270830_31270836del , CM000668.2:g.31270830_31270836del	GRCh38
NC_000006.11:g.31238607_31238613del , CM000668.1:g.31238607_31238613del	GRCh37
NC_000006.10:g.31346586_31346592del	NCBI36
NG_029422.2:g.6296_6302del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.619+237_619+243del MANE Select	ENSP00000365402.5:n.619+237_619+243del
ENST00000376228.9:c.619+237_619+243del	ENSP00000365402.5:n.619+237_619+243del
ENST00000376237.8:c.*206+237_*206+243del	ENSP00000365412.4:n.*206+237_*206+243del
ENST00000383329.7:c.619+237_619+243del	ENSP00000372819.3:n.619+237_619+243del
ENST00000415537.1:c.617+237_617+243del
ENST00000487245.5:n.978+237_978+243del
ENST00000495835.1:n.808+237_808+243del
NM_002117.5:c.619+237_619+243del	NP_002108.4:n.619+237_619+243del
NM_002117.6:c.619+237_619+243del MANE Select	NP_002108.4:n.619+237_619+243del