Canonical Allele Identifier: CA5955950

Gene: CD82

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.44605107G>A , CM000673.2:g.44605107G>A	GRCh38
NC_000011.9:g.44626657G>A , CM000673.1:g.44626657G>A	GRCh37
NC_000011.8:g.44583233G>A	NCBI36
NG_023234.1:g.44517G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227155.9:c.186G>A MANE Select	ENSP00000227155.4:p.Val62=
ENST00000227155.8:c.186G>A	ENSP00000227155.4:p.Val62=
ENST00000342935.7:c.186G>A	ENSP00000339686.3:p.Val62=
ENST00000524704.5:c.186G>A	ENSP00000436403.1:p.Val62=
ENST00000525813.5:c.186G>A	ENSP00000433804.1:p.Val62=
ENST00000525898.5:n.358G>A
ENST00000526958.5:c.309G>A	ENSP00000435682.1:p.Val103=
ENST00000527737.5:c.378G>A	ENSP00000433151.1:p.Val126=
ENST00000529277.5:n.125-13171G>A
ENST00000530601.1:c.129G>A	ENSP00000433788.1:p.Val43=
ENST00000530931.1:n.124G>A
ENST00000532544.5:c.186G>A	ENSP00000431767.1:p.Val62=
NM_001024844.1:c.186G>A	NP_001020015.1:p.Val62=
NM_002231.3:c.186G>A	NP_002222.1:p.Val62=
XM_006718222.1:c.309G>A	XP_006718285.1:p.Val103=
XM_006718223.1:c.186G>A	XP_006718286.1:p.Val62=
XM_011520067.1:c.93G>A	XP_011518369.1:p.Val31=
XM_006718223.2:c.186G>A	XP_006718286.1:p.Val62=
XM_011520067.2:c.93G>A	XP_011518369.1:p.Val31=
NM_002231.4:c.186G>A MANE Select	NP_002222.1:p.Val62=
NM_001024844.2:c.186G>A	NP_001020015.1:p.Val62=