Canonical Allele Identifier: CA1151505926

Gene: PLEKHG5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6474093T= , CM000663.2:g.6474093T=	GRCh38
NC_000001.10:g.6534153T= , CM000663.1:g.6534153T=	GRCh37
NC_000001.9:g.6456740T=	NCBI36
NG_007978.1:g.50917A= , LRG_262:g.50917A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.511A=	ENSP00000344570.5:p.Ile171=
ENST00000377728.8:c.511A= MANE Select	ENSP00000366957.3:p.Ile171=
ENST00000377740.5:c.511A=	ENSP00000366969.4:p.Ile171=
ENST00000377748.6:c.685A=	ENSP00000366977.2:p.Ile229=
ENST00000400913.6:c.511A=	ENSP00000383704.1:p.Ile171=
ENST00000400915.8:c.622A=	ENSP00000383706.4:p.Ile208=
ENST00000489097.6:n.987A=
ENST00000535355.6:c.718A=	ENSP00000441445.1:p.Ile240=
ENST00000537245.6:c.622A=	ENSP00000439625.2:p.Ile208=
ENST00000673471.2:c.808A=	ENSP00000500749.1:p.Ile270=
ENST00000674790.1:c.*723A=	ENSP00000502815.1:n.*723A=
ENST00000675123.1:c.511A=	ENSP00000502132.1:p.Ile171=
ENST00000675548.1:c.*339A=	ENSP00000502684.1:n.*339A=
ENST00000675694.1:c.511A=	ENSP00000501925.1:p.Ile171=
ENST00000340850.9:c.511A=	ENSP00000344570.5:p.Ile171=
ENST00000377725.5:c.511A=	ENSP00000366954.1:p.Ile171=
ENST00000377728.7:c.511A=	ENSP00000366957.3:p.Ile171=
ENST00000377732.5:c.622A=	ENSP00000366961.1:p.Ile208=
ENST00000377740.4:c.742A=	ENSP00000366969.3:p.Ile248=
ENST00000377748.5:c.742A=	ENSP00000366977.1:p.Ile248=
ENST00000400913.5:c.511A=	ENSP00000383704.1:p.Ile171=
ENST00000400915.7:c.679A=	ENSP00000383706.3:p.Ile227=
ENST00000489097.5:n.987A=
ENST00000535355.5:c.718A=	ENSP00000441445.1:p.Ile240=
ENST00000537245.5:c.748A=	ENSP00000439625.1:p.Ile250=
NM_001042663.1:c.679A=	NP_001036128.1:p.Ile227=
NM_001042664.1:c.511A=	NP_001036129.1:p.Ile171=
NM_001042665.1:c.511A=	NP_001036130.1:p.Ile171=
NM_001265592.1:c.748A=	NP_001252521.1:p.Ile250=
NM_001265593.1:c.718A=	NP_001252522.1:p.Ile240=
NM_001265594.1:c.511A=	NP_001252523.1:p.Ile171=
NM_020631.4:c.511A=	NP_065682.2:p.Ile171=
NM_198681.3:c.742A=	NP_941374.2:p.Ile248=
NM_001042663.2:c.679A=	NP_001036128.1:p.Ile227=
NM_001265594.2:c.511A=	NP_001252523.1:p.Ile171=
NM_020631.5:c.511A=	NP_065682.2:p.Ile171=
NM_001042663.3:c.622A=	NP_001036128.2:p.Ile208=
NM_001265592.2:c.622A=	NP_001252521.2:p.Ile208=
NM_020631.6:c.511A= MANE Select	NP_065682.2:p.Ile171=
NM_198681.4:c.511A=	NP_941374.3:p.Ile171=