Canonical Allele Identifier: CA1151505985

Gene: PLEKHG5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6474115G= , CM000663.2:g.6474115G=	GRCh38
NC_000001.10:g.6534175G= , CM000663.1:g.6534175G=	GRCh37
NC_000001.9:g.6456762G=	NCBI36
NG_007978.1:g.50895C= , LRG_262:g.50895C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.489C=	ENSP00000344570.5:p.Asp163=
ENST00000377728.8:c.489C= MANE Select	ENSP00000366957.3:p.Asp163=
ENST00000377740.5:c.489C=	ENSP00000366969.4:p.Asp163=
ENST00000377748.6:c.663C=	ENSP00000366977.2:p.Asp221=
ENST00000400913.6:c.489C=	ENSP00000383704.1:p.Asp163=
ENST00000400915.8:c.600C=	ENSP00000383706.4:p.Asp200=
ENST00000489097.6:n.965C=
ENST00000535355.6:c.696C=	ENSP00000441445.1:p.Asp232=
ENST00000537245.6:c.600C=	ENSP00000439625.2:p.Asp200=
ENST00000673471.2:c.786C=	ENSP00000500749.1:p.Asp262=
ENST00000674790.1:c.*701C=	ENSP00000502815.1:n.*701C=
ENST00000675123.1:c.489C=	ENSP00000502132.1:p.Asp163=
ENST00000675548.1:c.*317C=	ENSP00000502684.1:n.*317C=
ENST00000675694.1:c.489C=	ENSP00000501925.1:p.Asp163=
ENST00000340850.9:c.489C=	ENSP00000344570.5:p.Asp163=
ENST00000377725.5:c.489C=	ENSP00000366954.1:p.Asp163=
ENST00000377728.7:c.489C=	ENSP00000366957.3:p.Asp163=
ENST00000377732.5:c.600C=	ENSP00000366961.1:p.Asp200=
ENST00000377740.4:c.720C=	ENSP00000366969.3:p.Asp240=
ENST00000377748.5:c.720C=	ENSP00000366977.1:p.Asp240=
ENST00000400913.5:c.489C=	ENSP00000383704.1:p.Asp163=
ENST00000400915.7:c.657C=	ENSP00000383706.3:p.Asp219=
ENST00000489097.5:n.965C=
ENST00000535355.5:c.696C=	ENSP00000441445.1:p.Asp232=
ENST00000537245.5:c.726C=	ENSP00000439625.1:p.Asp242=
NM_001042663.1:c.657C=	NP_001036128.1:p.Asp219=
NM_001042664.1:c.489C=	NP_001036129.1:p.Asp163=
NM_001042665.1:c.489C=	NP_001036130.1:p.Asp163=
NM_001265592.1:c.726C=	NP_001252521.1:p.Asp242=
NM_001265593.1:c.696C=	NP_001252522.1:p.Asp232=
NM_001265594.1:c.489C=	NP_001252523.1:p.Asp163=
NM_020631.4:c.489C=	NP_065682.2:p.Asp163=
NM_198681.3:c.720C=	NP_941374.2:p.Asp240=
NM_001042663.2:c.657C=	NP_001036128.1:p.Asp219=
NM_001265594.2:c.489C=	NP_001252523.1:p.Asp163=
NM_020631.5:c.489C=	NP_065682.2:p.Asp163=
NM_001042663.3:c.600C=	NP_001036128.2:p.Asp200=
NM_001265592.2:c.600C=	NP_001252521.2:p.Asp200=
NM_020631.6:c.489C= MANE Select	NP_065682.2:p.Asp163=
NM_198681.4:c.489C=	NP_941374.3:p.Asp163=