Canonical Allele Identifier: CA1151524474
Gene: PLEKHG5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.6470588_6470597delinsTGCCGCTGCC , CM000663.2:g.6470588_6470597delinsTGCCGCTGCC GRCh38
NC_000001.10:g.6530648_6530657delinsTGCCGCTGCC , CM000663.1:g.6530648_6530657delinsTGCCGCTGCC GRCh37
NC_000001.9:g.6453235_6453244delinsTGCCGCTGCC NCBI36
NG_007978.1:g.54413_54422delinsGGCAGCGGCA , LRG_262:g.54413_54422delinsGGCAGCGGCA
NG_029910.1:g.599_608delinsGGCAGCGGCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000340850.10:c.1589_1598delinsGGCAGCGGCA ENSP00000344570.5:p.Arg530=
ENST00000377728.8:c.1589_1598delinsGGCAGCGGCA MANE Select ENSP00000366957.3:p.Arg530=
ENST00000377740.5:c.1589_1598delinsGGCAGCGGCA ENSP00000366969.4:p.Arg530=
ENST00000377748.6:c.1763_1772delinsGGCAGCGGCA ENSP00000366977.2:p.Arg588=
ENST00000400913.6:c.1589_1598delinsGGCAGCGGCA ENSP00000383704.1:p.Arg530=
ENST00000400915.8:c.1700_1709delinsGGCAGCGGCA ENSP00000383706.4:p.Arg567=
ENST00000489097.6:n.2065_2074delinsGGCAGCGGCA
ENST00000535355.6:c.1796_1805delinsGGCAGCGGCA ENSP00000441445.1:p.Arg599=
ENST00000537245.6:c.1700_1709delinsGGCAGCGGCA ENSP00000439625.2:p.Arg567=
ENST00000673471.2:c.1886_1895delinsGGCAGCGGCA ENSP00000500749.1:p.Arg629=
ENST00000674790.1:c.*1801_*1810delinsGGCAGCGGCA ENSP00000502815.1:n.*1801_*1810delinsGGCAGCGGCA
ENST00000674943.1:n.251_260delinsGGCAGCGGCA
ENST00000675123.1:c.1589_1598delinsGGCAGCGGCA ENSP00000502132.1:p.Arg530=
ENST00000675548.1:c.*1417_*1426delinsGGCAGCGGCA ENSP00000502684.1:n.*1417_*1426delinsGGCAGCGGCA
ENST00000675694.1:c.1589_1598delinsGGCAGCGGCA ENSP00000501925.1:p.Arg530=
ENST00000676401.1:n.136_145delinsGGCAGCGGCA
ENST00000340850.9:c.1589_1598delinsGGCAGCGGCA ENSP00000344570.5:p.Arg530=
ENST00000377725.5:c.1589_1598delinsGGCAGCGGCA ENSP00000366954.1:p.Arg530=
ENST00000377728.7:c.1589_1598delinsGGCAGCGGCA ENSP00000366957.3:p.Arg530=
ENST00000377732.5:c.1700_1709delinsGGCAGCGGCA ENSP00000366961.1:p.Arg567=
ENST00000377740.4:c.1820_1829delinsGGCAGCGGCA ENSP00000366969.3:p.Arg607=
ENST00000377748.5:c.1820_1829delinsGGCAGCGGCA ENSP00000366977.1:p.Arg607=
ENST00000400913.5:c.1589_1598delinsGGCAGCGGCA ENSP00000383704.1:p.Arg530=
ENST00000400915.7:c.1757_1766delinsGGCAGCGGCA ENSP00000383706.3:p.Arg586=
ENST00000487949.4:n.791_800delinsGGCAGCGGCA
ENST00000489097.5:n.2065_2074delinsGGCAGCGGCA
ENST00000535355.5:c.1796_1805delinsGGCAGCGGCA ENSP00000441445.1:p.Arg599=
ENST00000537245.5:c.1826_1835delinsGGCAGCGGCA ENSP00000439625.1:p.Arg609=
NM_001042663.1:c.1757_1766delinsGGCAGCGGCA NP_001036128.1:p.Arg586=
NM_001042664.1:c.1589_1598delinsGGCAGCGGCA NP_001036129.1:p.Arg530=
NM_001042665.1:c.1589_1598delinsGGCAGCGGCA NP_001036130.1:p.Arg530=
NM_001265592.1:c.1826_1835delinsGGCAGCGGCA NP_001252521.1:p.Arg609=
NM_001265593.1:c.1796_1805delinsGGCAGCGGCA NP_001252522.1:p.Arg599=
NM_001265594.1:c.1589_1598delinsGGCAGCGGCA NP_001252523.1:p.Arg530=
NM_020631.4:c.1589_1598delinsGGCAGCGGCA NP_065682.2:p.Arg530=
NM_198681.3:c.1820_1829delinsGGCAGCGGCA NP_941374.2:p.Arg607=
NM_001042663.2:c.1757_1766delinsGGCAGCGGCA NP_001036128.1:p.Arg586=
NM_001265594.2:c.1589_1598delinsGGCAGCGGCA NP_001252523.1:p.Arg530=
NM_020631.5:c.1589_1598delinsGGCAGCGGCA NP_065682.2:p.Arg530=
NM_001042663.3:c.1700_1709delinsGGCAGCGGCA NP_001036128.2:p.Arg567=
NM_001265592.2:c.1700_1709delinsGGCAGCGGCA NP_001252521.2:p.Arg567=
NM_020631.6:c.1589_1598delinsGGCAGCGGCA MANE Select NP_065682.2:p.Arg530=
NM_198681.4:c.1589_1598delinsGGCAGCGGCA NP_941374.3:p.Arg530=