Canonical Allele Identifier: CA1148453523
Gene: PLEKHG5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.6474465T= , CM000663.2:g.6474465T= GRCh38
NC_000001.10:g.6534525T= , CM000663.1:g.6534525T= GRCh37
NC_000001.9:g.6457112T= NCBI36
NG_007978.1:g.50545A= , LRG_262:g.50545A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000340850.10:c.425A= ENSP00000344570.5:p.Tyr142=
ENST00000377728.8:c.425A= MANE Select ENSP00000366957.3:p.Tyr142=
ENST00000377740.5:c.425A= ENSP00000366969.4:p.Tyr142=
ENST00000377748.6:c.599A= ENSP00000366977.2:p.Tyr200=
ENST00000400913.6:c.425A= ENSP00000383704.1:p.Tyr142=
ENST00000400915.8:c.536A= ENSP00000383706.4:p.Tyr179=
ENST00000489097.6:n.901A=
ENST00000535355.6:c.632A= ENSP00000441445.1:p.Tyr211=
ENST00000537245.6:c.536A= ENSP00000439625.2:p.Tyr179=
ENST00000673471.2:c.722A= ENSP00000500749.1:p.Tyr241=
ENST00000674790.1:c.*637A= ENSP00000502815.1:n.*637A=
ENST00000675123.1:c.425A= ENSP00000502132.1:p.Tyr142=
ENST00000675548.1:c.*253A= ENSP00000502684.1:n.*253A=
ENST00000675694.1:c.425A= ENSP00000501925.1:p.Tyr142=
ENST00000676255.1:c.387A= ENSP00000502459.1:n.387A=
ENST00000340850.9:c.425A= ENSP00000344570.5:p.Tyr142=
ENST00000377725.5:c.425A= ENSP00000366954.1:p.Tyr142=
ENST00000377728.7:c.425A= ENSP00000366957.3:p.Tyr142=
ENST00000377732.5:c.536A= ENSP00000366961.1:p.Tyr179=
ENST00000377740.4:c.656A= ENSP00000366969.3:p.Tyr219=
ENST00000377748.5:c.656A= ENSP00000366977.1:p.Tyr219=
ENST00000400913.5:c.425A= ENSP00000383704.1:p.Tyr142=
ENST00000400915.7:c.593A= ENSP00000383706.3:p.Tyr198=
ENST00000489097.5:n.901A=
ENST00000535355.5:c.632A= ENSP00000441445.1:p.Tyr211=
ENST00000537245.5:c.662A= ENSP00000439625.1:p.Tyr221=
NM_001042663.1:c.593A= NP_001036128.1:p.Tyr198=
NM_001042664.1:c.425A= NP_001036129.1:p.Tyr142=
NM_001042665.1:c.425A= NP_001036130.1:p.Tyr142=
NM_001265592.1:c.662A= NP_001252521.1:p.Tyr221=
NM_001265593.1:c.632A= NP_001252522.1:p.Tyr211=
NM_001265594.1:c.425A= NP_001252523.1:p.Tyr142=
NM_020631.4:c.425A= NP_065682.2:p.Tyr142=
NM_198681.3:c.656A= NP_941374.2:p.Tyr219=
NM_001042663.2:c.593A= NP_001036128.1:p.Tyr198=
NM_001265594.2:c.425A= NP_001252523.1:p.Tyr142=
NM_020631.5:c.425A= NP_065682.2:p.Tyr142=
NM_001042663.3:c.536A= NP_001036128.2:p.Tyr179=
NM_001265592.2:c.536A= NP_001252521.2:p.Tyr179=
NM_020631.6:c.425A= MANE Select NP_065682.2:p.Tyr142=
NM_198681.4:c.425A= NP_941374.3:p.Tyr142=