Canonical Allele Identifier: CA5819915

Gene: CD81

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2394108C>T , CM000673.2:g.2394108C>T	GRCh38
NC_000011.9:g.2415338C>T , CM000673.1:g.2415338C>T	GRCh37
NC_000011.8:g.2371914C>T	NCBI36
NG_023386.1:g.21792C>T , LRG_142:g.21792C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004356.4:c.195C>T MANE Select	NP_004347.1:p.Leu65=
ENST00000263645.10:c.195C>T MANE Select	ENSP00000263645.5:p.Leu65=
NM_001297649.1:c.-19C>T	NP_001284578.1:n.-19C>T
NM_001297649.2:c.-19C>T	NP_001284578.1:n.-19C>T
NM_004356.3:c.195C>T , LRG_142t1:c.195C>T	NP_004347.1:p.Leu65=
ENST00000263645.9:c.195C>T	ENSP00000263645.4:p.Leu65=
ENST00000381036.7:c.309C>T	ENSP00000370424.3:p.Leu103=
ENST00000464784.6:c.149C>T
ENST00000475945.6:c.-19C>T	ENSP00000433178.1:n.-19C>T
ENST00000475945.7:c.-19C>T	ENSP00000433178.2:n.-19C>T
ENST00000481687.1:c.213C>T	ENSP00000432033.1:p.Leu71=
ENST00000492252.5:c.174C>T	ENSP00000432249.1:p.Leu58=
ENST00000492627.5:c.-19C>T	ENSP00000437242.1:n.-19C>T
ENST00000493525.6:c.171C>T	ENSP00000432497.1:p.Leu57=
ENST00000524805.5:n.618C>T
ENST00000526072.5:c.-19C>T	ENSP00000431780.1:n.-19C>T
ENST00000527343.5:c.162C>T	ENSP00000433767.1:p.Leu54=
ENST00000530239.1:n.95C>T
ENST00000530648.5:c.-19C>T	ENSP00000432723.1:n.-19C>T
ENST00000531840.1:n.2726C>T
ENST00000533417.5:c.180C>T	ENSP00000435633.1:p.Leu60=
ENST00000533417.6:c.396C>T	ENSP00000435633.2:p.Leu132=
XM_011520492.1:c.174C>T	XP_011518794.1:p.Leu58=
XM_011520492.2:c.174C>T	XP_011518794.1:p.Leu58=