Canonical Allele Identifier: CA1151526599

Gene: PLEKHG5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6471058C= , CM000663.2:g.6471058C=	GRCh38
NC_000001.10:g.6531118C= , CM000663.1:g.6531118C=	GRCh37
NC_000001.9:g.6453705C=	NCBI36
NG_007978.1:g.53952G= , LRG_262:g.53952G=
NG_029910.1:g.138G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.1324G=	ENSP00000344570.5:p.Glu442=
ENST00000377728.8:c.1324G= MANE Select	ENSP00000366957.3:p.Glu442=
ENST00000377740.5:c.1324G=	ENSP00000366969.4:p.Glu442=
ENST00000377748.6:c.1498G=	ENSP00000366977.2:p.Glu500=
ENST00000400913.6:c.1324G=	ENSP00000383704.1:p.Glu442=
ENST00000400915.8:c.1435G=	ENSP00000383706.4:p.Glu479=
ENST00000489097.6:n.1800G=
ENST00000535355.6:c.1531G=	ENSP00000441445.1:p.Glu511=
ENST00000537245.6:c.1435G=	ENSP00000439625.2:p.Glu479=
ENST00000673471.2:c.1621G=	ENSP00000500749.1:p.Glu541=
ENST00000674685.1:n.357G=
ENST00000674790.1:c.*1536G=	ENSP00000502815.1:n.*1536G=
ENST00000675123.1:c.1324G=	ENSP00000502132.1:p.Glu442=
ENST00000675548.1:c.*1152G=	ENSP00000502684.1:n.*1152G=
ENST00000675694.1:c.1324G=	ENSP00000501925.1:p.Glu442=
ENST00000340850.9:c.1324G=	ENSP00000344570.5:p.Glu442=
ENST00000377725.5:c.1324G=	ENSP00000366954.1:p.Glu442=
ENST00000377728.7:c.1324G=	ENSP00000366957.3:p.Glu442=
ENST00000377732.5:c.1435G=	ENSP00000366961.1:p.Glu479=
ENST00000377740.4:c.1555G=	ENSP00000366969.3:p.Glu519=
ENST00000377748.5:c.1555G=	ENSP00000366977.1:p.Glu519=
ENST00000400913.5:c.1324G=	ENSP00000383704.1:p.Glu442=
ENST00000400915.7:c.1492G=	ENSP00000383706.3:p.Glu498=
ENST00000487949.4:n.526G=
ENST00000489097.5:n.1800G=
ENST00000535355.5:c.1531G=	ENSP00000441445.1:p.Glu511=
ENST00000537245.5:c.1561G=	ENSP00000439625.1:p.Glu521=
NM_001042663.1:c.1492G=	NP_001036128.1:p.Glu498=
NM_001042664.1:c.1324G=	NP_001036129.1:p.Glu442=
NM_001042665.1:c.1324G=	NP_001036130.1:p.Glu442=
NM_001265592.1:c.1561G=	NP_001252521.1:p.Glu521=
NM_001265593.1:c.1531G=	NP_001252522.1:p.Glu511=
NM_001265594.1:c.1324G=	NP_001252523.1:p.Glu442=
NM_020631.4:c.1324G=	NP_065682.2:p.Glu442=
NM_198681.3:c.1555G=	NP_941374.2:p.Glu519=
NM_001042663.2:c.1492G=	NP_001036128.1:p.Glu498=
NM_001265594.2:c.1324G=	NP_001252523.1:p.Glu442=
NM_020631.5:c.1324G=	NP_065682.2:p.Glu442=
NM_001042663.3:c.1435G=	NP_001036128.2:p.Glu479=
NM_001265592.2:c.1435G=	NP_001252521.2:p.Glu479=
NM_020631.6:c.1324G= MANE Select	NP_065682.2:p.Glu442=
NM_198681.4:c.1324G=	NP_941374.3:p.Glu442=