Canonical Allele Identifier: CA1145473198
Gene: PLEKHG5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.6474874G= , CM000663.2:g.6474874G= GRCh38
NC_000001.10:g.6534934G= , CM000663.1:g.6534934G= GRCh37
NC_000001.9:g.6457521G= NCBI36
NG_007978.1:g.50136C= , LRG_262:g.50136C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000340850.10:c.302+173C= ENSP00000344570.5:n.302+173C=
ENST00000377728.8:c.302+173C= MANE Select ENSP00000366957.3:n.302+173C=
ENST00000377740.5:c.302+173C= ENSP00000366969.4:n.302+173C=
ENST00000377748.6:c.476+173C= ENSP00000366977.2:n.476+173C=
ENST00000400913.6:c.302+173C= ENSP00000383704.1:n.302+173C=
ENST00000400915.8:c.413+173C= ENSP00000383706.4:n.413+173C=
ENST00000489097.6:n.492C=
ENST00000535355.6:c.509+173C= ENSP00000441445.1:n.509+173C=
ENST00000537245.6:c.413+173C= ENSP00000439625.2:n.413+173C=
ENST00000673471.2:c.599+173C= ENSP00000500749.1:n.599+173C=
ENST00000674790.1:c.*514+173C= ENSP00000502815.1:n.*514+173C=
ENST00000675093.1:c.302+173C= ENSP00000502687.1:n.302+173C=
ENST00000675123.1:c.302+173C= ENSP00000502132.1:n.302+173C=
ENST00000675548.1:c.*130+173C= ENSP00000502684.1:n.*130+173C=
ENST00000675694.1:c.302+173C= ENSP00000501925.1:n.302+173C=
ENST00000676255.1:c.129-42C= ENSP00000502459.1:n.129-42C=
ENST00000676287.1:c.302+173C= ENSP00000502810.1:n.302+173C=
ENST00000340850.9:c.302+173C= ENSP00000344570.5:n.302+173C=
ENST00000377725.5:c.302+173C= ENSP00000366954.1:n.302+173C=
ENST00000377728.7:c.302+173C= ENSP00000366957.3:n.302+173C=
ENST00000377732.5:c.413+173C= ENSP00000366961.1:n.413+173C=
ENST00000377740.4:c.533+173C= ENSP00000366969.3:n.533+173C=
ENST00000377748.5:c.533+173C= ENSP00000366977.1:n.533+173C=
ENST00000400913.5:c.302+173C= ENSP00000383704.1:n.302+173C=
ENST00000400915.7:c.470+173C= ENSP00000383706.3:n.470+173C=
ENST00000489097.5:n.492C=
ENST00000535355.5:c.509+173C= ENSP00000441445.1:n.509+173C=
ENST00000537245.5:c.539+173C= ENSP00000439625.1:n.539+173C=
NM_001042663.1:c.470+173C= NP_001036128.1:n.470+173C=
NM_001042664.1:c.302+173C= NP_001036129.1:n.302+173C=
NM_001042665.1:c.302+173C= NP_001036130.1:n.302+173C=
NM_001265592.1:c.539+173C= NP_001252521.1:n.539+173C=
NM_001265593.1:c.509+173C= NP_001252522.1:n.509+173C=
NM_001265594.1:c.302+173C= NP_001252523.1:n.302+173C=
NM_020631.4:c.302+173C= NP_065682.2:n.302+173C=
NM_198681.3:c.533+173C= NP_941374.2:n.533+173C=
NM_001042663.2:c.470+173C= NP_001036128.1:n.470+173C=
NM_001265594.2:c.302+173C= NP_001252523.1:n.302+173C=
NM_020631.5:c.302+173C= NP_065682.2:n.302+173C=
NM_001042663.3:c.413+173C= NP_001036128.2:n.413+173C=
NM_001265592.2:c.413+173C= NP_001252521.2:n.413+173C=
NM_020631.6:c.302+173C= MANE Select NP_065682.2:n.302+173C=
NM_198681.4:c.302+173C= NP_941374.3:n.302+173C=