Canonical Allele Identifier: CA1151524488
Gene: PLEKHG5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.6470592G= , CM000663.2:g.6470592G= GRCh38
NC_000001.10:g.6530652G= , CM000663.1:g.6530652G= GRCh37
NC_000001.9:g.6453239G= NCBI36
NG_007978.1:g.54418C= , LRG_262:g.54418C=
NG_029910.1:g.604C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000340850.10:c.1594C= ENSP00000344570.5:p.Arg532=
ENST00000377728.8:c.1594C= MANE Select ENSP00000366957.3:p.Arg532=
ENST00000377740.5:c.1594C= ENSP00000366969.4:p.Arg532=
ENST00000377748.6:c.1768C= ENSP00000366977.2:p.Arg590=
ENST00000400913.6:c.1594C= ENSP00000383704.1:p.Arg532=
ENST00000400915.8:c.1705C= ENSP00000383706.4:p.Arg569=
ENST00000489097.6:n.2070C=
ENST00000535355.6:c.1801C= ENSP00000441445.1:p.Arg601=
ENST00000537245.6:c.1705C= ENSP00000439625.2:p.Arg569=
ENST00000673471.2:c.1891C= ENSP00000500749.1:p.Arg631=
ENST00000674790.1:c.*1806C= ENSP00000502815.1:n.*1806C=
ENST00000674943.1:n.256C=
ENST00000675123.1:c.1594C= ENSP00000502132.1:p.Arg532=
ENST00000675548.1:c.*1422C= ENSP00000502684.1:n.*1422C=
ENST00000675694.1:c.1594C= ENSP00000501925.1:p.Arg532=
ENST00000676401.1:n.141C=
ENST00000340850.9:c.1594C= ENSP00000344570.5:p.Arg532=
ENST00000377725.5:c.1594C= ENSP00000366954.1:p.Arg532=
ENST00000377728.7:c.1594C= ENSP00000366957.3:p.Arg532=
ENST00000377732.5:c.1705C= ENSP00000366961.1:p.Arg569=
ENST00000377740.4:c.1825C= ENSP00000366969.3:p.Arg609=
ENST00000377748.5:c.1825C= ENSP00000366977.1:p.Arg609=
ENST00000400913.5:c.1594C= ENSP00000383704.1:p.Arg532=
ENST00000400915.7:c.1762C= ENSP00000383706.3:p.Arg588=
ENST00000487949.4:n.796C=
ENST00000489097.5:n.2070C=
ENST00000535355.5:c.1801C= ENSP00000441445.1:p.Arg601=
ENST00000537245.5:c.1831C= ENSP00000439625.1:p.Arg611=
NM_001042663.1:c.1762C= NP_001036128.1:p.Arg588=
NM_001042664.1:c.1594C= NP_001036129.1:p.Arg532=
NM_001042665.1:c.1594C= NP_001036130.1:p.Arg532=
NM_001265592.1:c.1831C= NP_001252521.1:p.Arg611=
NM_001265593.1:c.1801C= NP_001252522.1:p.Arg601=
NM_001265594.1:c.1594C= NP_001252523.1:p.Arg532=
NM_020631.4:c.1594C= NP_065682.2:p.Arg532=
NM_198681.3:c.1825C= NP_941374.2:p.Arg609=
NM_001042663.2:c.1762C= NP_001036128.1:p.Arg588=
NM_001265594.2:c.1594C= NP_001252523.1:p.Arg532=
NM_020631.5:c.1594C= NP_065682.2:p.Arg532=
NM_001042663.3:c.1705C= NP_001036128.2:p.Arg569=
NM_001265592.2:c.1705C= NP_001252521.2:p.Arg569=
NM_020631.6:c.1594C= MANE Select NP_065682.2:p.Arg532=
NM_198681.4:c.1594C= NP_941374.3:p.Arg532=