Canonical Allele Identifier: CA1151506919

Gene: PLEKHG5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6474490C= , CM000663.2:g.6474490C=	GRCh38
NC_000001.10:g.6534550C= , CM000663.1:g.6534550C=	GRCh37
NC_000001.9:g.6457137C=	NCBI36
NG_007978.1:g.50520G= , LRG_262:g.50520G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.400G=	ENSP00000344570.5:p.Glu134=
ENST00000377728.8:c.400G= MANE Select	ENSP00000366957.3:p.Glu134=
ENST00000377740.5:c.400G=	ENSP00000366969.4:p.Glu134=
ENST00000377748.6:c.574G=	ENSP00000366977.2:p.Glu192=
ENST00000400913.6:c.400G=	ENSP00000383704.1:p.Glu134=
ENST00000400915.8:c.511G=	ENSP00000383706.4:p.Glu171=
ENST00000489097.6:n.876G=
ENST00000535355.6:c.607G=	ENSP00000441445.1:p.Glu203=
ENST00000537245.6:c.511G=	ENSP00000439625.2:p.Glu171=
ENST00000673471.2:c.697G=	ENSP00000500749.1:p.Glu233=
ENST00000674790.1:c.*612G=	ENSP00000502815.1:n.*612G=
ENST00000675123.1:c.400G=	ENSP00000502132.1:p.Glu134=
ENST00000675548.1:c.*228G=	ENSP00000502684.1:n.*228G=
ENST00000675694.1:c.400G=	ENSP00000501925.1:p.Glu134=
ENST00000676255.1:c.362G=	ENSP00000502459.1:n.362G=
ENST00000340850.9:c.400G=	ENSP00000344570.5:p.Glu134=
ENST00000377725.5:c.400G=	ENSP00000366954.1:p.Glu134=
ENST00000377728.7:c.400G=	ENSP00000366957.3:p.Glu134=
ENST00000377732.5:c.511G=	ENSP00000366961.1:p.Glu171=
ENST00000377740.4:c.631G=	ENSP00000366969.3:p.Glu211=
ENST00000377748.5:c.631G=	ENSP00000366977.1:p.Glu211=
ENST00000400913.5:c.400G=	ENSP00000383704.1:p.Glu134=
ENST00000400915.7:c.568G=	ENSP00000383706.3:p.Glu190=
ENST00000489097.5:n.876G=
ENST00000535355.5:c.607G=	ENSP00000441445.1:p.Glu203=
ENST00000537245.5:c.637G=	ENSP00000439625.1:p.Glu213=
NM_001042663.1:c.568G=	NP_001036128.1:p.Glu190=
NM_001042664.1:c.400G=	NP_001036129.1:p.Glu134=
NM_001042665.1:c.400G=	NP_001036130.1:p.Glu134=
NM_001265592.1:c.637G=	NP_001252521.1:p.Glu213=
NM_001265593.1:c.607G=	NP_001252522.1:p.Glu203=
NM_001265594.1:c.400G=	NP_001252523.1:p.Glu134=
NM_020631.4:c.400G=	NP_065682.2:p.Glu134=
NM_198681.3:c.631G=	NP_941374.2:p.Glu211=
NM_001042663.2:c.568G=	NP_001036128.1:p.Glu190=
NM_001265594.2:c.400G=	NP_001252523.1:p.Glu134=
NM_020631.5:c.400G=	NP_065682.2:p.Glu134=
NM_001042663.3:c.511G=	NP_001036128.2:p.Glu171=
NM_001265592.2:c.511G=	NP_001252521.2:p.Glu171=
NM_020631.6:c.400G= MANE Select	NP_065682.2:p.Glu134=
NM_198681.4:c.400G=	NP_941374.3:p.Glu134=