Canonical Allele Identifier: CA561868
Gene: PLEKHG5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1521436
ClinVar RCV Id: RCV002031283
dbSNP Id: rs769529781
gnomAD v2: 1-6534535-C-T
gnomAD v4: 1-6474475-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.6474475C>T , CM000663.2:g.6474475C>T GRCh38
NC_000001.10:g.6534535C>T , CM000663.1:g.6534535C>T GRCh37
NC_000001.9:g.6457122C>T NCBI36
NG_007978.1:g.50535G>A , LRG_262:g.50535G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000340850.10:c.415G>A ENSP00000344570.5:p.Gly139Arg
ENST00000377728.8:c.415G>A MANE Select ENSP00000366957.3:p.Gly139Arg
ENST00000377740.5:c.415G>A ENSP00000366969.4:p.Gly139Arg
ENST00000377748.6:c.589G>A ENSP00000366977.2:p.Gly197Arg
ENST00000400913.6:c.415G>A ENSP00000383704.1:p.Gly139Arg
ENST00000400915.8:c.526G>A ENSP00000383706.4:p.Gly176Arg
ENST00000489097.6:n.891G>A
ENST00000535355.6:c.622G>A ENSP00000441445.1:p.Gly208Arg
ENST00000537245.6:c.526G>A ENSP00000439625.2:p.Gly176Arg
ENST00000673471.2:c.712G>A ENSP00000500749.1:p.Gly238Arg
ENST00000674790.1:c.*627G>A ENSP00000502815.1:n.*627G>A
ENST00000675123.1:c.415G>A ENSP00000502132.1:p.Gly139Arg
ENST00000675548.1:c.*243G>A ENSP00000502684.1:n.*243G>A
ENST00000675694.1:c.415G>A ENSP00000501925.1:p.Gly139Arg
ENST00000676255.1:c.377G>A ENSP00000502459.1:n.377G>A
ENST00000340850.9:c.415G>A ENSP00000344570.5:p.Gly139Arg
ENST00000377725.5:c.415G>A ENSP00000366954.1:p.Gly139Arg
ENST00000377728.7:c.415G>A ENSP00000366957.3:p.Gly139Arg
ENST00000377732.5:c.526G>A ENSP00000366961.1:p.Gly176Arg
ENST00000377740.4:c.646G>A ENSP00000366969.3:p.Gly216Arg
ENST00000377748.5:c.646G>A ENSP00000366977.1:p.Gly216Arg
ENST00000400913.5:c.415G>A ENSP00000383704.1:p.Gly139Arg
ENST00000400915.7:c.583G>A ENSP00000383706.3:p.Gly195Arg
ENST00000489097.5:n.891G>A
ENST00000535355.5:c.622G>A ENSP00000441445.1:p.Gly208Arg
ENST00000537245.5:c.652G>A ENSP00000439625.1:p.Gly218Arg
NM_001042663.1:c.583G>A NP_001036128.1:p.Gly195Arg
NM_001042664.1:c.415G>A NP_001036129.1:p.Gly139Arg
NM_001042665.1:c.415G>A NP_001036130.1:p.Gly139Arg
NM_001265592.1:c.652G>A NP_001252521.1:p.Gly218Arg
NM_001265593.1:c.622G>A NP_001252522.1:p.Gly208Arg
NM_001265594.1:c.415G>A NP_001252523.1:p.Gly139Arg
NM_020631.4:c.415G>A NP_065682.2:p.Gly139Arg
NM_198681.3:c.646G>A NP_941374.2:p.Gly216Arg
NM_001042663.2:c.583G>A NP_001036128.1:p.Gly195Arg
NM_001265594.2:c.415G>A NP_001252523.1:p.Gly139Arg
NM_020631.5:c.415G>A NP_065682.2:p.Gly139Arg
NM_001042663.3:c.526G>A NP_001036128.2:p.Gly176Arg
NM_001265592.2:c.526G>A NP_001252521.2:p.Gly176Arg
NM_020631.6:c.415G>A MANE Select NP_065682.2:p.Gly139Arg
NM_198681.4:c.415G>A NP_941374.3:p.Gly139Arg