Canonical Allele Identifier: CA1151505988
Gene: PLEKHG5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.6474117C= , CM000663.2:g.6474117C= GRCh38
NC_000001.10:g.6534177C= , CM000663.1:g.6534177C= GRCh37
NC_000001.9:g.6456764C= NCBI36
NG_007978.1:g.50893G= , LRG_262:g.50893G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000340850.10:c.487G= ENSP00000344570.5:p.Asp163=
ENST00000377728.8:c.487G= MANE Select ENSP00000366957.3:p.Asp163=
ENST00000377740.5:c.487G= ENSP00000366969.4:p.Asp163=
ENST00000377748.6:c.661G= ENSP00000366977.2:p.Asp221=
ENST00000400913.6:c.487G= ENSP00000383704.1:p.Asp163=
ENST00000400915.8:c.598G= ENSP00000383706.4:p.Asp200=
ENST00000489097.6:n.963G=
ENST00000535355.6:c.694G= ENSP00000441445.1:p.Asp232=
ENST00000537245.6:c.598G= ENSP00000439625.2:p.Asp200=
ENST00000673471.2:c.784G= ENSP00000500749.1:p.Asp262=
ENST00000674790.1:c.*699G= ENSP00000502815.1:n.*699G=
ENST00000675123.1:c.487G= ENSP00000502132.1:p.Asp163=
ENST00000675548.1:c.*315G= ENSP00000502684.1:n.*315G=
ENST00000675694.1:c.487G= ENSP00000501925.1:p.Asp163=
ENST00000340850.9:c.487G= ENSP00000344570.5:p.Asp163=
ENST00000377725.5:c.487G= ENSP00000366954.1:p.Asp163=
ENST00000377728.7:c.487G= ENSP00000366957.3:p.Asp163=
ENST00000377732.5:c.598G= ENSP00000366961.1:p.Asp200=
ENST00000377740.4:c.718G= ENSP00000366969.3:p.Asp240=
ENST00000377748.5:c.718G= ENSP00000366977.1:p.Asp240=
ENST00000400913.5:c.487G= ENSP00000383704.1:p.Asp163=
ENST00000400915.7:c.655G= ENSP00000383706.3:p.Asp219=
ENST00000489097.5:n.963G=
ENST00000535355.5:c.694G= ENSP00000441445.1:p.Asp232=
ENST00000537245.5:c.724G= ENSP00000439625.1:p.Asp242=
NM_001042663.1:c.655G= NP_001036128.1:p.Asp219=
NM_001042664.1:c.487G= NP_001036129.1:p.Asp163=
NM_001042665.1:c.487G= NP_001036130.1:p.Asp163=
NM_001265592.1:c.724G= NP_001252521.1:p.Asp242=
NM_001265593.1:c.694G= NP_001252522.1:p.Asp232=
NM_001265594.1:c.487G= NP_001252523.1:p.Asp163=
NM_020631.4:c.487G= NP_065682.2:p.Asp163=
NM_198681.3:c.718G= NP_941374.2:p.Asp240=
NM_001042663.2:c.655G= NP_001036128.1:p.Asp219=
NM_001265594.2:c.487G= NP_001252523.1:p.Asp163=
NM_020631.5:c.487G= NP_065682.2:p.Asp163=
NM_001042663.3:c.598G= NP_001036128.2:p.Asp200=
NM_001265592.2:c.598G= NP_001252521.2:p.Asp200=
NM_020631.6:c.487G= MANE Select NP_065682.2:p.Asp163=
NM_198681.4:c.487G= NP_941374.3:p.Asp163=