Canonical Allele Identifier: CA338138716
Gene: PLEKHG5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.6474102T>A , CM000663.2:g.6474102T>A GRCh38
NC_000001.10:g.6534162T>A , CM000663.1:g.6534162T>A GRCh37
NC_000001.9:g.6456749T>A NCBI36
NG_007978.1:g.50908A>T , LRG_262:g.50908A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000340850.10:c.502A>T ENSP00000344570.5:p.Ser168Cys
ENST00000377728.8:c.502A>T MANE Select ENSP00000366957.3:p.Ser168Cys
ENST00000377740.5:c.502A>T ENSP00000366969.4:p.Ser168Cys
ENST00000377748.6:c.676A>T ENSP00000366977.2:p.Ser226Cys
ENST00000400913.6:c.502A>T ENSP00000383704.1:p.Ser168Cys
ENST00000400915.8:c.613A>T ENSP00000383706.4:p.Ser205Cys
ENST00000489097.6:n.978A>T
ENST00000535355.6:c.709A>T ENSP00000441445.1:p.Ser237Cys
ENST00000537245.6:c.613A>T ENSP00000439625.2:p.Ser205Cys
ENST00000673471.2:c.799A>T ENSP00000500749.1:p.Ser267Cys
ENST00000674790.1:c.*714A>T ENSP00000502815.1:n.*714A>T
ENST00000675123.1:c.502A>T ENSP00000502132.1:p.Ser168Cys
ENST00000675548.1:c.*330A>T ENSP00000502684.1:n.*330A>T
ENST00000675694.1:c.502A>T ENSP00000501925.1:p.Ser168Cys
ENST00000340850.9:c.502A>T ENSP00000344570.5:p.Ser168Cys
ENST00000377725.5:c.502A>T ENSP00000366954.1:p.Ser168Cys
ENST00000377728.7:c.502A>T ENSP00000366957.3:p.Ser168Cys
ENST00000377732.5:c.613A>T ENSP00000366961.1:p.Ser205Cys
ENST00000377740.4:c.733A>T ENSP00000366969.3:p.Ser245Cys
ENST00000377748.5:c.733A>T ENSP00000366977.1:p.Ser245Cys
ENST00000400913.5:c.502A>T ENSP00000383704.1:p.Ser168Cys
ENST00000400915.7:c.670A>T ENSP00000383706.3:p.Ser224Cys
ENST00000489097.5:n.978A>T
ENST00000535355.5:c.709A>T ENSP00000441445.1:p.Ser237Cys
ENST00000537245.5:c.739A>T ENSP00000439625.1:p.Ser247Cys
NM_001042663.1:c.670A>T NP_001036128.1:p.Ser224Cys
NM_001042664.1:c.502A>T NP_001036129.1:p.Ser168Cys
NM_001042665.1:c.502A>T NP_001036130.1:p.Ser168Cys
NM_001265592.1:c.739A>T NP_001252521.1:p.Ser247Cys
NM_001265593.1:c.709A>T NP_001252522.1:p.Ser237Cys
NM_001265594.1:c.502A>T NP_001252523.1:p.Ser168Cys
NM_020631.4:c.502A>T NP_065682.2:p.Ser168Cys
NM_198681.3:c.733A>T NP_941374.2:p.Ser245Cys
NM_001042663.2:c.670A>T NP_001036128.1:p.Ser224Cys
NM_001265594.2:c.502A>T NP_001252523.1:p.Ser168Cys
NM_020631.5:c.502A>T NP_065682.2:p.Ser168Cys
NM_001042663.3:c.613A>T NP_001036128.2:p.Ser205Cys
NM_001265592.2:c.613A>T NP_001252521.2:p.Ser205Cys
NM_020631.6:c.502A>T MANE Select NP_065682.2:p.Ser168Cys
NM_198681.4:c.502A>T NP_941374.3:p.Ser168Cys