Canonical Allele Identifier: CA1151514046

Gene: PLEKHG5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6477604A= , CM000663.2:g.6477604A=	GRCh38
NC_000001.10:g.6537664A= , CM000663.1:g.6537664A=	GRCh37
NC_000001.9:g.6460251A=	NCBI36
NG_007978.1:g.47406T= , LRG_262:g.47406T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.-33T=	ENSP00000344570.5:n.-33T=
ENST00000377728.8:c.-33T= MANE Select	ENSP00000366957.3:n.-33T=
ENST00000377740.5:c.-33T=	ENSP00000366969.4:n.-33T=
ENST00000377748.6:c.79T=	ENSP00000366977.2:p.Cys27=
ENST00000400913.6:c.-33T=	ENSP00000383704.1:n.-33T=
ENST00000400915.8:c.79T=	ENSP00000383706.4:p.Cys27=
ENST00000535355.6:c.175T=	ENSP00000441445.1:p.Cys59=
ENST00000537245.6:c.79T=	ENSP00000439625.2:p.Cys27=
ENST00000673471.2:c.265T=	ENSP00000500749.1:p.Cys89=
ENST00000674790.1:c.*180T=	ENSP00000502815.1:n.*180T=
ENST00000674803.1:n.198T=
ENST00000675093.1:c.-33T=	ENSP00000502687.1:n.-33T=
ENST00000675123.1:c.-33T=	ENSP00000502132.1:n.-33T=
ENST00000675548.1:c.153T=	ENSP00000502684.1:p.Ser51=
ENST00000675655.1:n.174T=
ENST00000675694.1:c.-33T=	ENSP00000501925.1:n.-33T=
ENST00000676287.1:c.-33T=	ENSP00000502810.1:n.-33T=
ENST00000676362.1:n.191T=
ENST00000340850.9:c.-33T=	ENSP00000344570.5:n.-33T=
ENST00000377725.5:c.-33T=	ENSP00000366954.1:n.-33T=
ENST00000377728.7:c.-33T=	ENSP00000366957.3:n.-33T=
ENST00000377732.5:c.79T=	ENSP00000366961.1:p.Cys27=
ENST00000377740.4:c.199T=	ENSP00000366969.3:p.Cys67=
ENST00000377748.5:c.199T=	ENSP00000366977.1:p.Cys67=
ENST00000400913.5:c.-33T=	ENSP00000383704.1:n.-33T=
ENST00000400915.7:c.136T=	ENSP00000383706.3:p.Cys46=
ENST00000535355.5:c.175T=	ENSP00000441445.1:p.Cys59=
ENST00000537245.5:c.205T=	ENSP00000439625.1:p.Cys69=
NM_001042663.1:c.136T=	NP_001036128.1:p.Cys46=
NM_001042664.1:c.-33T=	NP_001036129.1:n.-33T=
NM_001042665.1:c.-33T=	NP_001036130.1:n.-33T=
NM_001265592.1:c.205T=	NP_001252521.1:p.Cys69=
NM_001265593.1:c.175T=	NP_001252522.1:p.Cys59=
NM_001265594.1:c.-33T=	NP_001252523.1:n.-33T=
NM_020631.4:c.-33T=	NP_065682.2:n.-33T=
NM_198681.3:c.199T=	NP_941374.2:p.Cys67=
NM_001042663.2:c.136T=	NP_001036128.1:p.Cys46=
NM_001265594.2:c.-33T=	NP_001252523.1:n.-33T=
NM_020631.5:c.-33T=	NP_065682.2:n.-33T=
NM_001042663.3:c.79T=	NP_001036128.2:p.Cys27=
NM_001265592.2:c.79T=	NP_001252521.2:p.Cys27=
NM_020631.6:c.-33T= MANE Select	NP_065682.2:n.-33T=
NM_198681.4:c.-33T=	NP_941374.3:n.-33T=