Canonical Allele Identifier: CA1151513907

Gene: PLEKHG5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6477552A= , CM000663.2:g.6477552A=	GRCh38
NC_000001.10:g.6537612A= , CM000663.1:g.6537612A=	GRCh37
NC_000001.9:g.6460199A=	NCBI36
NG_007978.1:g.47458T= , LRG_262:g.47458T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.20T=	ENSP00000344570.5:p.Val7=
ENST00000377728.8:c.20T= MANE Select	ENSP00000366957.3:p.Val7=
ENST00000377740.5:c.20T=	ENSP00000366969.4:p.Val7=
ENST00000377748.6:c.131T=	ENSP00000366977.2:p.Val44=
ENST00000400913.6:c.20T=	ENSP00000383704.1:p.Val7=
ENST00000400915.8:c.131T=	ENSP00000383706.4:p.Val44=
ENST00000489097.6:n.37T=
ENST00000535355.6:c.227T=	ENSP00000441445.1:p.Val76=
ENST00000537245.6:c.131T=	ENSP00000439625.2:p.Val44=
ENST00000673471.2:c.317T=	ENSP00000500749.1:p.Val106=
ENST00000674790.1:c.*232T=	ENSP00000502815.1:n.*232T=
ENST00000674803.1:n.250T=
ENST00000675093.1:c.20T=	ENSP00000502687.1:p.Val7=
ENST00000675123.1:c.20T=	ENSP00000502132.1:p.Val7=
ENST00000675548.1:c.205T=	ENSP00000502684.1:p.Ser69=
ENST00000675655.1:n.226T=
ENST00000675694.1:c.20T=	ENSP00000501925.1:p.Val7=
ENST00000676287.1:c.20T=	ENSP00000502810.1:p.Val7=
ENST00000676362.1:n.243T=
ENST00000340850.9:c.20T=	ENSP00000344570.5:p.Val7=
ENST00000377725.5:c.20T=	ENSP00000366954.1:p.Val7=
ENST00000377728.7:c.20T=	ENSP00000366957.3:p.Val7=
ENST00000377732.5:c.131T=	ENSP00000366961.1:p.Val44=
ENST00000377740.4:c.251T=	ENSP00000366969.3:p.Val84=
ENST00000377748.5:c.251T=	ENSP00000366977.1:p.Val84=
ENST00000400913.5:c.20T=	ENSP00000383704.1:p.Val7=
ENST00000400915.7:c.188T=	ENSP00000383706.3:p.Val63=
ENST00000489097.5:n.37T=
ENST00000535355.5:c.227T=	ENSP00000441445.1:p.Val76=
ENST00000537245.5:c.257T=	ENSP00000439625.1:p.Val86=
NM_001042663.1:c.188T=	NP_001036128.1:p.Val63=
NM_001042664.1:c.20T=	NP_001036129.1:p.Val7=
NM_001042665.1:c.20T=	NP_001036130.1:p.Val7=
NM_001265592.1:c.257T=	NP_001252521.1:p.Val86=
NM_001265593.1:c.227T=	NP_001252522.1:p.Val76=
NM_001265594.1:c.20T=	NP_001252523.1:p.Val7=
NM_020631.4:c.20T=	NP_065682.2:p.Val7=
NM_198681.3:c.251T=	NP_941374.2:p.Val84=
NM_001042663.2:c.188T=	NP_001036128.1:p.Val63=
NM_001265594.2:c.20T=	NP_001252523.1:p.Val7=
NM_020631.5:c.20T=	NP_065682.2:p.Val7=
NM_001042663.3:c.131T=	NP_001036128.2:p.Val44=
NM_001265592.2:c.131T=	NP_001252521.2:p.Val44=
NM_020631.6:c.20T= MANE Select	NP_065682.2:p.Val7=
NM_198681.4:c.20T=	NP_941374.3:p.Val7=