Canonical Allele Identifier: CA2642985248
Gene: PLEKHG5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.6473954_6473955insAGGGGCGCCTGCCTCTGAGGAGGGGCT , CM000663.2:g.6473954_6473955insAGGGGCGCCTGCCTCTGAGGAGGGGCT GRCh38
NC_000001.10:g.6534014_6534015insAGGGGCGCCTGCCTCTGAGGAGGGGCT , CM000663.1:g.6534014_6534015insAGGGGCGCCTGCCTCTGAGGAGGGGCT GRCh37
NC_000001.9:g.6456601_6456602insAGGGGCGCCTGCCTCTGAGGAGGGGCT NCBI36
NG_007978.1:g.51074_51075insGCGCCCCTAGCCCCTCCTCAGAGGCAG , LRG_262:g.51074_51075insGCGCCCCTAGCCCCTCCTCAGAGGCAG

Transcript Alleles

HGVS Amino-acid change
ENST00000340850.10:c.591+77_591+78insGCGCCCCTAGCCCCTCCTCAGAGGCAG ENSP00000344570.5:n.591+77_591+78insGCGCC...
ENST00000377728.8:c.591+77_591+78insGCGCCCCTAGCCCCTCCTCAGAGGCAG MANE Select ENSP00000366957.3:n.591+77_591+78insGCGCC...
ENST00000377740.5:c.591+77_591+78insGCGCCCCTAGCCCCTCCTCAGAGGCAG ENSP00000366969.4:n.591+77_591+78insGCGCC...
ENST00000377748.6:c.765+77_765+78insGCGCCCCTAGCCCCTCCTCAGAGGCAG ENSP00000366977.2:n.765+77_765+78insGCGCC...
ENST00000400913.6:c.591+77_591+78insGCGCCCCTAGCCCCTCCTCAGAGGCAG ENSP00000383704.1:n.591+77_591+78insGCGCC...
ENST00000400915.8:c.702+77_702+78insGCGCCCCTAGCCCCTCCTCAGAGGCAG ENSP00000383706.4:n.702+77_702+78insGCGCC...
ENST00000489097.6:n.1067+77_1067+78insGCGCCCCTAGCCCCTCCTCAGAGGCAG
ENST00000535355.6:c.798+77_798+78insGCGCCCCTAGCCCCTCCTCAGAGGCAG ENSP00000441445.1:n.798+77_798+78insGCGCC...
ENST00000537245.6:c.702+77_702+78insGCGCCCCTAGCCCCTCCTCAGAGGCAG ENSP00000439625.2:n.702+77_702+78insGCGCC...
ENST00000673471.2:c.888+77_888+78insGCGCCCCTAGCCCCTCCTCAGAGGCAG ENSP00000500749.1:n.888+77_888+78insGCGCC...
ENST00000674790.1:c.*803+77_*803+78insGCGCCCCTAGCCCCTCCTCAGAGGCAG ENSP00000502815.1:n.*803+77_*803+78insGCG...
ENST00000675123.1:c.591+77_591+78insGCGCCCCTAGCCCCTCCTCAGAGGCAG ENSP00000502132.1:n.591+77_591+78insGCGCC...
ENST00000675548.1:c.*419+77_*419+78insGCGCCCCTAGCCCCTCCTCAGAGGCAG ENSP00000502684.1:n.*419+77_*419+78insGCG...
ENST00000675694.1:c.591+77_591+78insGCGCCCCTAGCCCCTCCTCAGAGGCAG ENSP00000501925.1:n.591+77_591+78insGCGCC...
ENST00000340850.9:c.591+77_591+78insGCGCCCCTAGCCCCTCCTCAGAGGCAG ENSP00000344570.5:n.591+77_591+78insGCGCC...
ENST00000377725.5:c.591+77_591+78insGCGCCCCTAGCCCCTCCTCAGAGGCAG ENSP00000366954.1:n.591+77_591+78insGCGCC...
ENST00000377728.7:c.591+77_591+78insGCGCCCCTAGCCCCTCCTCAGAGGCAG ENSP00000366957.3:n.591+77_591+78insGCGCC...
ENST00000377732.5:c.702+77_702+78insGCGCCCCTAGCCCCTCCTCAGAGGCAG ENSP00000366961.1:n.702+77_702+78insGCGCC...
ENST00000377740.4:c.822+77_822+78insGCGCCCCTAGCCCCTCCTCAGAGGCAG ENSP00000366969.3:n.822+77_822+78insGCGCC...
ENST00000377748.5:c.822+77_822+78insGCGCCCCTAGCCCCTCCTCAGAGGCAG ENSP00000366977.1:n.822+77_822+78insGCGCC...
ENST00000400913.5:c.591+77_591+78insGCGCCCCTAGCCCCTCCTCAGAGGCAG ENSP00000383704.1:n.591+77_591+78insGCGCC...
ENST00000400915.7:c.759+77_759+78insGCGCCCCTAGCCCCTCCTCAGAGGCAG ENSP00000383706.3:n.759+77_759+78insGCGCC...
ENST00000489097.5:n.1067+77_1067+78insGCGCCCCTAGCCCCTCCTCAGAGGCAG
ENST00000535355.5:c.798+77_798+78insGCGCCCCTAGCCCCTCCTCAGAGGCAG ENSP00000441445.1:n.798+77_798+78insGCGCC...
ENST00000537245.5:c.828+77_828+78insGCGCCCCTAGCCCCTCCTCAGAGGCAG ENSP00000439625.1:n.828+77_828+78insGCGCC...
NM_001042663.1:c.759+77_759+78insGCGCCCCTAGCCCCTCCTCAGAGGCAG NP_001036128.1:n.759+77_759+78insGCGCCCCT...
NM_001042664.1:c.591+77_591+78insGCGCCCCTAGCCCCTCCTCAGAGGCAG NP_001036129.1:n.591+77_591+78insGCGCCCCT...
NM_001042665.1:c.591+77_591+78insGCGCCCCTAGCCCCTCCTCAGAGGCAG NP_001036130.1:n.591+77_591+78insGCGCCCCT...
NM_001265592.1:c.828+77_828+78insGCGCCCCTAGCCCCTCCTCAGAGGCAG NP_001252521.1:n.828+77_828+78insGCGCCCCT...
NM_001265593.1:c.798+77_798+78insGCGCCCCTAGCCCCTCCTCAGAGGCAG NP_001252522.1:n.798+77_798+78insGCGCCCCT...
NM_001265594.1:c.591+77_591+78insGCGCCCCTAGCCCCTCCTCAGAGGCAG NP_001252523.1:n.591+77_591+78insGCGCCCCT...
NM_020631.4:c.591+77_591+78insGCGCCCCTAGCCCCTCCTCAGAGGCAG NP_065682.2:n.591+77_591+78insGCGCCCCTAGC...
NM_198681.3:c.822+77_822+78insGCGCCCCTAGCCCCTCCTCAGAGGCAG NP_941374.2:n.822+77_822+78insGCGCCCCTAGC...
NM_001042663.2:c.759+77_759+78insGCGCCCCTAGCCCCTCCTCAGAGGCAG NP_001036128.1:n.759+77_759+78insGCGCCCCT...
NM_001265594.2:c.591+77_591+78insGCGCCCCTAGCCCCTCCTCAGAGGCAG NP_001252523.1:n.591+77_591+78insGCGCCCCT...
NM_020631.5:c.591+77_591+78insGCGCCCCTAGCCCCTCCTCAGAGGCAG NP_065682.2:n.591+77_591+78insGCGCCCCTAGC...
NM_001042663.3:c.702+77_702+78insGCGCCCCTAGCCCCTCCTCAGAGGCAG NP_001036128.2:n.702+77_702+78insGCGCCCCT...
NM_001265592.2:c.702+77_702+78insGCGCCCCTAGCCCCTCCTCAGAGGCAG NP_001252521.2:n.702+77_702+78insGCGCCCCT...
NM_020631.6:c.591+77_591+78insGCGCCCCTAGCCCCTCCTCAGAGGCAG MANE Select NP_065682.2:n.591+77_591+78insGCGCCCCTAGC...
NM_198681.4:c.591+77_591+78insGCGCCCCTAGCCCCTCCTCAGAGGCAG NP_941374.3:n.591+77_591+78insGCGCCCCTAGC...