Canonical Allele Identifier: CA338138656
Gene: PLEKHG5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.6474086C>A , CM000663.2:g.6474086C>A GRCh38
NC_000001.10:g.6534146C>A , CM000663.1:g.6534146C>A GRCh37
NC_000001.9:g.6456733C>A NCBI36
NG_007978.1:g.50924G>T , LRG_262:g.50924G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000340850.10:c.518G>T ENSP00000344570.5:p.Arg173Leu
ENST00000377728.8:c.518G>T MANE Select ENSP00000366957.3:p.Arg173Leu
ENST00000377740.5:c.518G>T ENSP00000366969.4:p.Arg173Leu
ENST00000377748.6:c.692G>T ENSP00000366977.2:p.Arg231Leu
ENST00000400913.6:c.518G>T ENSP00000383704.1:p.Arg173Leu
ENST00000400915.8:c.629G>T ENSP00000383706.4:p.Arg210Leu
ENST00000489097.6:n.994G>T
ENST00000535355.6:c.725G>T ENSP00000441445.1:p.Arg242Leu
ENST00000537245.6:c.629G>T ENSP00000439625.2:p.Arg210Leu
ENST00000673471.2:c.815G>T ENSP00000500749.1:p.Arg272Leu
ENST00000674790.1:c.*730G>T ENSP00000502815.1:n.*730G>T
ENST00000675123.1:c.518G>T ENSP00000502132.1:p.Arg173Leu
ENST00000675548.1:c.*346G>T ENSP00000502684.1:n.*346G>T
ENST00000675694.1:c.518G>T ENSP00000501925.1:p.Arg173Leu
ENST00000340850.9:c.518G>T ENSP00000344570.5:p.Arg173Leu
ENST00000377725.5:c.518G>T ENSP00000366954.1:p.Arg173Leu
ENST00000377728.7:c.518G>T ENSP00000366957.3:p.Arg173Leu
ENST00000377732.5:c.629G>T ENSP00000366961.1:p.Arg210Leu
ENST00000377740.4:c.749G>T ENSP00000366969.3:p.Arg250Leu
ENST00000377748.5:c.749G>T ENSP00000366977.1:p.Arg250Leu
ENST00000400913.5:c.518G>T ENSP00000383704.1:p.Arg173Leu
ENST00000400915.7:c.686G>T ENSP00000383706.3:p.Arg229Leu
ENST00000489097.5:n.994G>T
ENST00000535355.5:c.725G>T ENSP00000441445.1:p.Arg242Leu
ENST00000537245.5:c.755G>T ENSP00000439625.1:p.Arg252Leu
NM_001042663.1:c.686G>T NP_001036128.1:p.Arg229Leu
NM_001042664.1:c.518G>T NP_001036129.1:p.Arg173Leu
NM_001042665.1:c.518G>T NP_001036130.1:p.Arg173Leu
NM_001265592.1:c.755G>T NP_001252521.1:p.Arg252Leu
NM_001265593.1:c.725G>T NP_001252522.1:p.Arg242Leu
NM_001265594.1:c.518G>T NP_001252523.1:p.Arg173Leu
NM_020631.4:c.518G>T NP_065682.2:p.Arg173Leu
NM_198681.3:c.749G>T NP_941374.2:p.Arg250Leu
NM_001042663.2:c.686G>T NP_001036128.1:p.Arg229Leu
NM_001265594.2:c.518G>T NP_001252523.1:p.Arg173Leu
NM_020631.5:c.518G>T NP_065682.2:p.Arg173Leu
NM_001042663.3:c.629G>T NP_001036128.2:p.Arg210Leu
NM_001265592.2:c.629G>T NP_001252521.2:p.Arg210Leu
NM_020631.6:c.518G>T MANE Select NP_065682.2:p.Arg173Leu
NM_198681.4:c.518G>T NP_941374.3:p.Arg173Leu