Canonical Allele Identifier: CA1151507041

Gene: PLEKHG5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6474557C= , CM000663.2:g.6474557C=	GRCh38
NC_000001.10:g.6534617C= , CM000663.1:g.6534617C=	GRCh37
NC_000001.9:g.6457204C=	NCBI36
NG_007978.1:g.50453G= , LRG_262:g.50453G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.333G=	ENSP00000344570.5:p.Lys111=
ENST00000377728.8:c.333G= MANE Select	ENSP00000366957.3:p.Lys111=
ENST00000377740.5:c.333G=	ENSP00000366969.4:p.Lys111=
ENST00000377748.6:c.507G=	ENSP00000366977.2:p.Lys169=
ENST00000400913.6:c.333G=	ENSP00000383704.1:p.Lys111=
ENST00000400915.8:c.444G=	ENSP00000383706.4:p.Lys148=
ENST00000489097.6:n.809G=
ENST00000535355.6:c.540G=	ENSP00000441445.1:p.Lys180=
ENST00000537245.6:c.444G=	ENSP00000439625.2:p.Lys148=
ENST00000673471.2:c.630G=	ENSP00000500749.1:p.Lys210=
ENST00000674790.1:c.*545G=	ENSP00000502815.1:n.*545G=
ENST00000675123.1:c.333G=	ENSP00000502132.1:p.Lys111=
ENST00000675548.1:c.*161G=	ENSP00000502684.1:n.*161G=
ENST00000675694.1:c.333G=	ENSP00000501925.1:p.Lys111=
ENST00000676255.1:c.295G=	ENSP00000502459.1:n.295G=
ENST00000340850.9:c.333G=	ENSP00000344570.5:p.Lys111=
ENST00000377725.5:c.333G=	ENSP00000366954.1:p.Lys111=
ENST00000377728.7:c.333G=	ENSP00000366957.3:p.Lys111=
ENST00000377732.5:c.444G=	ENSP00000366961.1:p.Lys148=
ENST00000377740.4:c.564G=	ENSP00000366969.3:p.Lys188=
ENST00000377748.5:c.564G=	ENSP00000366977.1:p.Lys188=
ENST00000400913.5:c.333G=	ENSP00000383704.1:p.Lys111=
ENST00000400915.7:c.501G=	ENSP00000383706.3:p.Lys167=
ENST00000489097.5:n.809G=
ENST00000535355.5:c.540G=	ENSP00000441445.1:p.Lys180=
ENST00000537245.5:c.570G=	ENSP00000439625.1:p.Lys190=
NM_001042663.1:c.501G=	NP_001036128.1:p.Lys167=
NM_001042664.1:c.333G=	NP_001036129.1:p.Lys111=
NM_001042665.1:c.333G=	NP_001036130.1:p.Lys111=
NM_001265592.1:c.570G=	NP_001252521.1:p.Lys190=
NM_001265593.1:c.540G=	NP_001252522.1:p.Lys180=
NM_001265594.1:c.333G=	NP_001252523.1:p.Lys111=
NM_020631.4:c.333G=	NP_065682.2:p.Lys111=
NM_198681.3:c.564G=	NP_941374.2:p.Lys188=
NM_001042663.2:c.501G=	NP_001036128.1:p.Lys167=
NM_001265594.2:c.333G=	NP_001252523.1:p.Lys111=
NM_020631.5:c.333G=	NP_065682.2:p.Lys111=
NM_001042663.3:c.444G=	NP_001036128.2:p.Lys148=
NM_001265592.2:c.444G=	NP_001252521.2:p.Lys148=
NM_020631.6:c.333G= MANE Select	NP_065682.2:p.Lys111=
NM_198681.4:c.333G=	NP_941374.3:p.Lys111=