Canonical Allele Identifier: CA5819963

Gene: CD81

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2395063A>G , CM000673.2:g.2395063A>G	GRCh38
NC_000011.9:g.2416293A>G , CM000673.1:g.2416293A>G	GRCh37
NC_000011.8:g.2372869A>G	NCBI36
NG_023386.1:g.22747A>G , LRG_142:g.22747A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_004356.4:c.354+17A>G MANE Select	NP_004347.1:n.354+17A>G
ENST00000263645.10:c.354+17A>G MANE Select	ENSP00000263645.5:n.354+17A>G
NM_001297649.1:c.141+17A>G	NP_001284578.1:n.141+17A>G
NM_001297649.2:c.141+17A>G	NP_001284578.1:n.141+17A>G
NM_004356.3:c.354+17A>G , LRG_142t1:c.354+17A>G	NP_004347.1:n.354+17A>G
ENST00000263645.9:c.354+17A>G	ENSP00000263645.4:n.354+17A>G
ENST00000381036.7:c.468+17A>G	ENSP00000370424.3:n.468+17A>G
ENST00000464784.6:c.308+17A>G
ENST00000468153.1:n.197+17A>G
ENST00000475945.6:c.141+17A>G	ENSP00000433178.1:n.141+17A>G
ENST00000475945.7:c.141+17A>G	ENSP00000433178.2:n.141+17A>G
ENST00000481687.1:c.372+17A>G	ENSP00000432033.1:n.372+17A>G
ENST00000492252.5:c.333+17A>G	ENSP00000432249.1:n.333+17A>G
ENST00000492627.5:c.141+17A>G	ENSP00000437242.1:n.141+17A>G
ENST00000524805.5:n.777+17A>G
ENST00000526072.5:c.141+17A>G	ENSP00000431780.1:n.141+17A>G
ENST00000527343.5:c.321+17A>G	ENSP00000433767.1:n.321+17A>G
ENST00000530239.1:n.254+17A>G
ENST00000530648.5:c.141+17A>G	ENSP00000432723.1:n.141+17A>G
ENST00000531840.1:n.2902A>G
ENST00000533417.5:c.339+17A>G	ENSP00000435633.1:n.339+17A>G
ENST00000533417.6:c.555+17A>G	ENSP00000435633.2:n.555+17A>G
XM_011520492.1:c.333+17A>G	XP_011518794.1:n.333+17A>G
XM_011520492.2:c.333+17A>G	XP_011518794.1:n.333+17A>G