Canonical Allele Identifier: CA1142047050
Gene: PLEKHG5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.6473053T= , CM000663.2:g.6473053T= GRCh38
NC_000001.10:g.6533113T= , CM000663.1:g.6533113T= GRCh37
NC_000001.9:g.6455700T= NCBI36
NG_007978.1:g.51957A= , LRG_262:g.51957A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000340850.10:c.917A= ENSP00000344570.5:p.Asp306=
ENST00000377728.8:c.917A= MANE Select ENSP00000366957.3:p.Asp306=
ENST00000377740.5:c.917A= ENSP00000366969.4:p.Asp306=
ENST00000377748.6:c.1091A= ENSP00000366977.2:p.Asp364=
ENST00000400913.6:c.917A= ENSP00000383704.1:p.Asp306=
ENST00000400915.8:c.1028A= ENSP00000383706.4:p.Asp343=
ENST00000489097.6:n.1393A=
ENST00000535355.6:c.1124A= ENSP00000441445.1:p.Asp375=
ENST00000537245.6:c.1028A= ENSP00000439625.2:p.Asp343=
ENST00000673471.2:c.1214A= ENSP00000500749.1:p.Asp405=
ENST00000674790.1:c.*1129A= ENSP00000502815.1:n.*1129A=
ENST00000675123.1:c.917A= ENSP00000502132.1:p.Asp306=
ENST00000675548.1:c.*745A= ENSP00000502684.1:n.*745A=
ENST00000675694.1:c.917A= ENSP00000501925.1:p.Asp306=
ENST00000340850.9:c.917A= ENSP00000344570.5:p.Asp306=
ENST00000377725.5:c.917A= ENSP00000366954.1:p.Asp306=
ENST00000377728.7:c.917A= ENSP00000366957.3:p.Asp306=
ENST00000377732.5:c.1028A= ENSP00000366961.1:p.Asp343=
ENST00000377740.4:c.1148A= ENSP00000366969.3:p.Asp383=
ENST00000377748.5:c.1148A= ENSP00000366977.1:p.Asp383=
ENST00000400913.5:c.917A= ENSP00000383704.1:p.Asp306=
ENST00000400915.7:c.1085A= ENSP00000383706.3:p.Asp362=
ENST00000489097.5:n.1393A=
ENST00000535355.5:c.1124A= ENSP00000441445.1:p.Asp375=
ENST00000537245.5:c.1154A= ENSP00000439625.1:p.Asp385=
NM_001042663.1:c.1085A= NP_001036128.1:p.Asp362=
NM_001042664.1:c.917A= NP_001036129.1:p.Asp306=
NM_001042665.1:c.917A= NP_001036130.1:p.Asp306=
NM_001265592.1:c.1154A= NP_001252521.1:p.Asp385=
NM_001265593.1:c.1124A= NP_001252522.1:p.Asp375=
NM_001265594.1:c.917A= NP_001252523.1:p.Asp306=
NM_020631.4:c.917A= NP_065682.2:p.Asp306=
NM_198681.3:c.1148A= NP_941374.2:p.Asp383=
NM_001042663.2:c.1085A= NP_001036128.1:p.Asp362=
NM_001265594.2:c.917A= NP_001252523.1:p.Asp306=
NM_020631.5:c.917A= NP_065682.2:p.Asp306=
NM_001042663.3:c.1028A= NP_001036128.2:p.Asp343=
NM_001265592.2:c.1028A= NP_001252521.2:p.Asp343=
NM_020631.6:c.917A= MANE Select NP_065682.2:p.Asp306=
NM_198681.4:c.917A= NP_941374.3:p.Asp306=