Canonical Allele Identifier: CA2542304024

Gene: PLEKHG5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6477589_6477590insAGGGCGTCATAAGGACAA , CM000663.2:g.6477589_6477590insAGGGCGTCATAAGGACAA	GRCh38
NC_000001.10:g.6537649_6537650insAGGGCGTCATAAGGACAA , CM000663.1:g.6537649_6537650insAGGGCGTCATAAGGACAA	GRCh37
NC_000001.9:g.6460236_6460237insAGGGCGTCATAAGGACAA	NCBI36
NG_007978.1:g.47420_47421insTTGTCCTTATGACGCCCT , LRG_262:g.47420_47421insTTGTCCTTATGACGCCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.-19_-18insTTGTCCTTATGACGCCCT	ENSP00000344570.5:n.-19_-18insTTGTCCTTATGACGCCCT
ENST00000377728.8:c.-19_-18insTTGTCCTTATGACGCCCT MANE Select	ENSP00000366957.3:n.-19_-18insTTGTCCTTATGACGCCCT
ENST00000377740.5:c.-19_-18insTTGTCCTTATGACGCCCT	ENSP00000366969.4:n.-19_-18insTTGTCCTTATGACGCCCT
ENST00000377748.6:c.93_94insTTGTCCTTATGACGCCCT
ENST00000400913.6:c.-19_-18insTTGTCCTTATGACGCCCT	ENSP00000383704.1:n.-19_-18insTTGTCCTTATGACGCCCT
ENST00000400915.8:c.93_94insTTGTCCTTATGACGCCCT
ENST00000535355.6:c.189_190insTTGTCCTTATGACGCCCT
ENST00000537245.6:c.93_94insTTGTCCTTATGACGCCCT
ENST00000673471.2:c.279_280insTTGTCCTTATGACGCCCT
ENST00000674790.1:c.*194_*195insTTGTCCTTATGACGCCCT	ENSP00000502815.1:n.*194_*195insTTGTCCTTATGACGCCCT
ENST00000674803.1:n.212_213insTTGTCCTTATGACGCCCT
ENST00000675093.1:c.-19_-18insTTGTCCTTATGACGCCCT	ENSP00000502687.1:n.-19_-18insTTGTCCTTATGACGCCCT
ENST00000675123.1:c.-19_-18insTTGTCCTTATGACGCCCT	ENSP00000502132.1:n.-19_-18insTTGTCCTTATGACGCCCT
ENST00000675548.1:c.167_168insTTGTCCTTATGACGCCCT	ENSP00000502684.1:p.Thr56_Ala57insCysProTyrAspAlaLeu
ENST00000675655.1:n.188_189insTTGTCCTTATGACGCCCT
ENST00000675694.1:c.-19_-18insTTGTCCTTATGACGCCCT	ENSP00000501925.1:n.-19_-18insTTGTCCTTATGACGCCCT
ENST00000676287.1:c.-19_-18insTTGTCCTTATGACGCCCT	ENSP00000502810.1:n.-19_-18insTTGTCCTTATGACGCCCT
ENST00000676362.1:n.205_206insTTGTCCTTATGACGCCCT
ENST00000340850.9:c.-19_-18insTTGTCCTTATGACGCCCT	ENSP00000344570.5:n.-19_-18insTTGTCCTTATGACGCCCT
ENST00000377725.5:c.-19_-18insTTGTCCTTATGACGCCCT	ENSP00000366954.1:n.-19_-18insTTGTCCTTATGACGCCCT
ENST00000377728.7:c.-19_-18insTTGTCCTTATGACGCCCT	ENSP00000366957.3:n.-19_-18insTTGTCCTTATGACGCCCT
ENST00000377732.5:c.93_94insTTGTCCTTATGACGCCCT
ENST00000377740.4:c.213_214insTTGTCCTTATGACGCCCT
ENST00000377748.5:c.213_214insTTGTCCTTATGACGCCCT
ENST00000400913.5:c.-19_-18insTTGTCCTTATGACGCCCT	ENSP00000383704.1:n.-19_-18insTTGTCCTTATGACGCCCT
ENST00000400915.7:c.150_151insTTGTCCTTATGACGCCCT
ENST00000535355.5:c.189_190insTTGTCCTTATGACGCCCT
ENST00000537245.5:c.219_220insTTGTCCTTATGACGCCCT
NM_001042663.1:c.150_151insTTGTCCTTATGACGCCCT
NM_001042664.1:c.-19_-18insTTGTCCTTATGACGCCCT	NP_001036129.1:n.-19_-18insTTGTCCTTATGACGCCCT
NM_001042665.1:c.-19_-18insTTGTCCTTATGACGCCCT	NP_001036130.1:n.-19_-18insTTGTCCTTATGACGCCCT
NM_001265592.1:c.219_220insTTGTCCTTATGACGCCCT
NM_001265593.1:c.189_190insTTGTCCTTATGACGCCCT
NM_001265594.1:c.-19_-18insTTGTCCTTATGACGCCCT	NP_001252523.1:n.-19_-18insTTGTCCTTATGACGCCCT
NM_020631.4:c.-19_-18insTTGTCCTTATGACGCCCT	NP_065682.2:n.-19_-18insTTGTCCTTATGACGCCCT
NM_198681.3:c.213_214insTTGTCCTTATGACGCCCT
NM_001042663.2:c.150_151insTTGTCCTTATGACGCCCT
NM_001265594.2:c.-19_-18insTTGTCCTTATGACGCCCT	NP_001252523.1:n.-19_-18insTTGTCCTTATGACGCCCT
NM_020631.5:c.-19_-18insTTGTCCTTATGACGCCCT	NP_065682.2:n.-19_-18insTTGTCCTTATGACGCCCT
NM_001042663.3:c.93_94insTTGTCCTTATGACGCCCT
NM_001265592.2:c.93_94insTTGTCCTTATGACGCCCT
NM_020631.6:c.-19_-18insTTGTCCTTATGACGCCCT MANE Select	NP_065682.2:n.-19_-18insTTGTCCTTATGACGCCCT
NM_198681.4:c.-19_-18insTTGTCCTTATGACGCCCT	NP_941374.3:n.-19_-18insTTGTCCTTATGACGCCCT