Canonical Allele Identifier: CA1151503956

Gene: PLEKHG5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6473360_6473411delinsGGCAGAGAGCAGCTGGAGGGCGTGGGGGGCTCCTGCCCGGGGATGCTCGCCT , CM000663.2:g.6473360_6473411delinsGGCAGAGAGCAGCTGGAGGGCGTGGGGGGCTCCTGCCCGGGGATGCTCGCCT	GRCh38
NC_000001.10:g.6533420_6533471delinsGGCAGAGAGCAGCTGGAGGGCGTGGGGGGCTCCTGCCCGGGGATGCTCGCCT , CM000663.1:g.6533420_6533471delinsGGCAGAGAGCAGCTGGAGGGCGTGGGGGGCTCCTGCCCGGGGATGCTCGCCT	GRCh37
NC_000001.9:g.6456007_6456058delinsGGCAGAGAGCAGCTGGAGGGCGTGGGGGGCTCCTGCCCGGGGATGCTCGCCT	NCBI36
NG_007978.1:g.51599_51650delinsAGGCGAGCATCCCCGGGCAGGAGCCCCCCACGCCCTCCAGCTGCTCTCTGCC , LRG_262:g.51599_51650delinsAGGCGAGCATCCCCGGGCAGGAGCCCCCCACGCCCTCCAGCTGCTCTCTGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.635_686delinsAGGCGAGCATCCCCGGGCAGGAGCCCCCCACGCCCTCCAGCTGCTCTCTGCC	ENSP00000344570.5:p.Glu212=
ENST00000377728.8:c.635_686delinsAGGCGAGCATCCCCGGGCAGGAGCCCCCCACGCCCTCCAGCTGCTCTCTGCC MANE Select	ENSP00000366957.3:p.Glu212=
ENST00000377740.5:c.635_686delinsAGGCGAGCATCCCCGGGCAGGAGCCCCCCACGCCCTCCAGCTGCTCTCTGCC	ENSP00000366969.4:p.Glu212=
ENST00000377748.6:c.809_860delinsAGGCGAGCATCCCCGGGCAGGAGCCCCCCACGCCCTCCAGCTGCTCTCTGCC	ENSP00000366977.2:p.Glu270=
ENST00000400913.6:c.635_686delinsAGGCGAGCATCCCCGGGCAGGAGCCCCCCACGCCCTCCAGCTGCTCTCTGCC	ENSP00000383704.1:p.Glu212=
ENST00000400915.8:c.746_797delinsAGGCGAGCATCCCCGGGCAGGAGCCCCCCACGCCCTCCAGCTGCTCTCTGCC	ENSP00000383706.4:p.Glu249=
ENST00000489097.6:n.1111_1162delinsAGGCGAGCATCCCCGGGCAGGAGCCCCCCACGCCCTCCAGCTGCTCTCTGCC
ENST00000535355.6:c.842_893delinsAGGCGAGCATCCCCGGGCAGGAGCCCCCCACGCCCTCCAGCTGCTCTCTGCC	ENSP00000441445.1:p.Glu281=
ENST00000537245.6:c.746_797delinsAGGCGAGCATCCCCGGGCAGGAGCCCCCCACGCCCTCCAGCTGCTCTCTGCC	ENSP00000439625.2:p.Glu249=
ENST00000673471.2:c.932_983delinsAGGCGAGCATCCCCGGGCAGGAGCCCCCCACGCCCTCCAGCTGCTCTCTGCC	ENSP00000500749.1:p.Glu311=
ENST00000674790.1:c.*847_*898delinsAGGCGAGCATCCCCGGGCAGGAGCCCCCCACGCCCTCCAGCTGCTCTCTGCC	ENSP00000502815.1:n.*847_*898delinsAGGCGAGCATCCCCGGGCAGGAGCCC...
ENST00000675123.1:c.635_686delinsAGGCGAGCATCCCCGGGCAGGAGCCCCCCACGCCCTCCAGCTGCTCTCTGCC	ENSP00000502132.1:p.Glu212=
ENST00000675548.1:c.*463_*514delinsAGGCGAGCATCCCCGGGCAGGAGCCCCCCACGCCCTCCAGCTGCTCTCTGCC	ENSP00000502684.1:n.*463_*514delinsAGGCGAGCATCCCCGGGCAGGAGCCC...
ENST00000675694.1:c.635_686delinsAGGCGAGCATCCCCGGGCAGGAGCCCCCCACGCCCTCCAGCTGCTCTCTGCC	ENSP00000501925.1:p.Glu212=
ENST00000340850.9:c.635_686delinsAGGCGAGCATCCCCGGGCAGGAGCCCCCCACGCCCTCCAGCTGCTCTCTGCC	ENSP00000344570.5:p.Glu212=
ENST00000377725.5:c.635_686delinsAGGCGAGCATCCCCGGGCAGGAGCCCCCCACGCCCTCCAGCTGCTCTCTGCC	ENSP00000366954.1:p.Glu212=
ENST00000377728.7:c.635_686delinsAGGCGAGCATCCCCGGGCAGGAGCCCCCCACGCCCTCCAGCTGCTCTCTGCC	ENSP00000366957.3:p.Glu212=
ENST00000377732.5:c.746_797delinsAGGCGAGCATCCCCGGGCAGGAGCCCCCCACGCCCTCCAGCTGCTCTCTGCC	ENSP00000366961.1:p.Glu249=
ENST00000377740.4:c.866_917delinsAGGCGAGCATCCCCGGGCAGGAGCCCCCCACGCCCTCCAGCTGCTCTCTGCC	ENSP00000366969.3:p.Glu289=
ENST00000377748.5:c.866_917delinsAGGCGAGCATCCCCGGGCAGGAGCCCCCCACGCCCTCCAGCTGCTCTCTGCC	ENSP00000366977.1:p.Glu289=
ENST00000400913.5:c.635_686delinsAGGCGAGCATCCCCGGGCAGGAGCCCCCCACGCCCTCCAGCTGCTCTCTGCC	ENSP00000383704.1:p.Glu212=
ENST00000400915.7:c.803_854delinsAGGCGAGCATCCCCGGGCAGGAGCCCCCCACGCCCTCCAGCTGCTCTCTGCC	ENSP00000383706.3:p.Glu268=
ENST00000489097.5:n.1111_1162delinsAGGCGAGCATCCCCGGGCAGGAGCCCCCCACGCCCTCCAGCTGCTCTCTGCC
ENST00000535355.5:c.842_893delinsAGGCGAGCATCCCCGGGCAGGAGCCCCCCACGCCCTCCAGCTGCTCTCTGCC	ENSP00000441445.1:p.Glu281=
ENST00000537245.5:c.872_923delinsAGGCGAGCATCCCCGGGCAGGAGCCCCCCACGCCCTCCAGCTGCTCTCTGCC	ENSP00000439625.1:p.Glu291=
NM_001042663.1:c.803_854delinsAGGCGAGCATCCCCGGGCAGGAGCCCCCCACGCCCTCCAGCTGCTCTCTGCC	NP_001036128.1:p.Glu268=
NM_001042664.1:c.635_686delinsAGGCGAGCATCCCCGGGCAGGAGCCCCCCACGCCCTCCAGCTGCTCTCTGCC	NP_001036129.1:p.Glu212=
NM_001042665.1:c.635_686delinsAGGCGAGCATCCCCGGGCAGGAGCCCCCCACGCCCTCCAGCTGCTCTCTGCC	NP_001036130.1:p.Glu212=
NM_001265592.1:c.872_923delinsAGGCGAGCATCCCCGGGCAGGAGCCCCCCACGCCCTCCAGCTGCTCTCTGCC	NP_001252521.1:p.Glu291=
NM_001265593.1:c.842_893delinsAGGCGAGCATCCCCGGGCAGGAGCCCCCCACGCCCTCCAGCTGCTCTCTGCC	NP_001252522.1:p.Glu281=
NM_001265594.1:c.635_686delinsAGGCGAGCATCCCCGGGCAGGAGCCCCCCACGCCCTCCAGCTGCTCTCTGCC	NP_001252523.1:p.Glu212=
NM_020631.4:c.635_686delinsAGGCGAGCATCCCCGGGCAGGAGCCCCCCACGCCCTCCAGCTGCTCTCTGCC	NP_065682.2:p.Glu212=
NM_198681.3:c.866_917delinsAGGCGAGCATCCCCGGGCAGGAGCCCCCCACGCCCTCCAGCTGCTCTCTGCC	NP_941374.2:p.Glu289=
NM_001042663.2:c.803_854delinsAGGCGAGCATCCCCGGGCAGGAGCCCCCCACGCCCTCCAGCTGCTCTCTGCC	NP_001036128.1:p.Glu268=
NM_001265594.2:c.635_686delinsAGGCGAGCATCCCCGGGCAGGAGCCCCCCACGCCCTCCAGCTGCTCTCTGCC	NP_001252523.1:p.Glu212=
NM_020631.5:c.635_686delinsAGGCGAGCATCCCCGGGCAGGAGCCCCCCACGCCCTCCAGCTGCTCTCTGCC	NP_065682.2:p.Glu212=
NM_001042663.3:c.746_797delinsAGGCGAGCATCCCCGGGCAGGAGCCCCCCACGCCCTCCAGCTGCTCTCTGCC	NP_001036128.2:p.Glu249=
NM_001265592.2:c.746_797delinsAGGCGAGCATCCCCGGGCAGGAGCCCCCCACGCCCTCCAGCTGCTCTCTGCC	NP_001252521.2:p.Glu249=
NM_020631.6:c.635_686delinsAGGCGAGCATCCCCGGGCAGGAGCCCCCCACGCCCTCCAGCTGCTCTCTGCC MANE Select	NP_065682.2:p.Glu212=
NM_198681.4:c.635_686delinsAGGCGAGCATCCCCGGGCAGGAGCCCCCCACGCCCTCCAGCTGCTCTCTGCC	NP_941374.3:p.Glu212=