Canonical Allele Identifier: CA1151503936

Gene: PLEKHG5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6473351_6473360delinsCTGCCGCTGG , CM000663.2:g.6473351_6473360delinsCTGCCGCTGG	GRCh38
NC_000001.10:g.6533411_6533420delinsCTGCCGCTGG , CM000663.1:g.6533411_6533420delinsCTGCCGCTGG	GRCh37
NC_000001.9:g.6455998_6456007delinsCTGCCGCTGG	NCBI36
NG_007978.1:g.51650_51659delinsCCAGCGGCAG , LRG_262:g.51650_51659delinsCCAGCGGCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.686_695delinsCCAGCGGCAG	ENSP00000344570.5:p.Pro229=
ENST00000377728.8:c.686_695delinsCCAGCGGCAG MANE Select	ENSP00000366957.3:p.Pro229=
ENST00000377740.5:c.686_695delinsCCAGCGGCAG	ENSP00000366969.4:p.Pro229=
ENST00000377748.6:c.860_869delinsCCAGCGGCAG	ENSP00000366977.2:p.Pro287=
ENST00000400913.6:c.686_695delinsCCAGCGGCAG	ENSP00000383704.1:p.Pro229=
ENST00000400915.8:c.797_806delinsCCAGCGGCAG	ENSP00000383706.4:p.Pro266=
ENST00000489097.6:n.1162_1171delinsCCAGCGGCAG
ENST00000535355.6:c.893_902delinsCCAGCGGCAG	ENSP00000441445.1:p.Pro298=
ENST00000537245.6:c.797_806delinsCCAGCGGCAG	ENSP00000439625.2:p.Pro266=
ENST00000673471.2:c.983_992delinsCCAGCGGCAG	ENSP00000500749.1:p.Pro328=
ENST00000674790.1:c.*898_*907delinsCCAGCGGCAG	ENSP00000502815.1:n.*898_*907delinsCCAGCGGCAG
ENST00000675123.1:c.686_695delinsCCAGCGGCAG	ENSP00000502132.1:p.Pro229=
ENST00000675548.1:c.*514_*523delinsCCAGCGGCAG	ENSP00000502684.1:n.*514_*523delinsCCAGCGGCAG
ENST00000675694.1:c.686_695delinsCCAGCGGCAG	ENSP00000501925.1:p.Pro229=
ENST00000340850.9:c.686_695delinsCCAGCGGCAG	ENSP00000344570.5:p.Pro229=
ENST00000377725.5:c.686_695delinsCCAGCGGCAG	ENSP00000366954.1:p.Pro229=
ENST00000377728.7:c.686_695delinsCCAGCGGCAG	ENSP00000366957.3:p.Pro229=
ENST00000377732.5:c.797_806delinsCCAGCGGCAG	ENSP00000366961.1:p.Pro266=
ENST00000377740.4:c.917_926delinsCCAGCGGCAG	ENSP00000366969.3:p.Pro306=
ENST00000377748.5:c.917_926delinsCCAGCGGCAG	ENSP00000366977.1:p.Pro306=
ENST00000400913.5:c.686_695delinsCCAGCGGCAG	ENSP00000383704.1:p.Pro229=
ENST00000400915.7:c.854_863delinsCCAGCGGCAG	ENSP00000383706.3:p.Pro285=
ENST00000489097.5:n.1162_1171delinsCCAGCGGCAG
ENST00000535355.5:c.893_902delinsCCAGCGGCAG	ENSP00000441445.1:p.Pro298=
ENST00000537245.5:c.923_932delinsCCAGCGGCAG	ENSP00000439625.1:p.Pro308=
NM_001042663.1:c.854_863delinsCCAGCGGCAG	NP_001036128.1:p.Pro285=
NM_001042664.1:c.686_695delinsCCAGCGGCAG	NP_001036129.1:p.Pro229=
NM_001042665.1:c.686_695delinsCCAGCGGCAG	NP_001036130.1:p.Pro229=
NM_001265592.1:c.923_932delinsCCAGCGGCAG	NP_001252521.1:p.Pro308=
NM_001265593.1:c.893_902delinsCCAGCGGCAG	NP_001252522.1:p.Pro298=
NM_001265594.1:c.686_695delinsCCAGCGGCAG	NP_001252523.1:p.Pro229=
NM_020631.4:c.686_695delinsCCAGCGGCAG	NP_065682.2:p.Pro229=
NM_198681.3:c.917_926delinsCCAGCGGCAG	NP_941374.2:p.Pro306=
NM_001042663.2:c.854_863delinsCCAGCGGCAG	NP_001036128.1:p.Pro285=
NM_001265594.2:c.686_695delinsCCAGCGGCAG	NP_001252523.1:p.Pro229=
NM_020631.5:c.686_695delinsCCAGCGGCAG	NP_065682.2:p.Pro229=
NM_001042663.3:c.797_806delinsCCAGCGGCAG	NP_001036128.2:p.Pro266=
NM_001265592.2:c.797_806delinsCCAGCGGCAG	NP_001252521.2:p.Pro266=
NM_020631.6:c.686_695delinsCCAGCGGCAG MANE Select	NP_065682.2:p.Pro229=
NM_198681.4:c.686_695delinsCCAGCGGCAG	NP_941374.3:p.Pro229=