Canonical Allele Identifier: CA338139201
Gene: PLEKHG5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.6474496T>G , CM000663.2:g.6474496T>G GRCh38
NC_000001.10:g.6534556T>G , CM000663.1:g.6534556T>G GRCh37
NC_000001.9:g.6457143T>G NCBI36
NG_007978.1:g.50514A>C , LRG_262:g.50514A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000340850.10:c.394A>C ENSP00000344570.5:p.Thr132Pro
ENST00000377728.8:c.394A>C MANE Select ENSP00000366957.3:p.Thr132Pro
ENST00000377740.5:c.394A>C ENSP00000366969.4:p.Thr132Pro
ENST00000377748.6:c.568A>C ENSP00000366977.2:p.Thr190Pro
ENST00000400913.6:c.394A>C ENSP00000383704.1:p.Thr132Pro
ENST00000400915.8:c.505A>C ENSP00000383706.4:p.Thr169Pro
ENST00000489097.6:n.870A>C
ENST00000535355.6:c.601A>C ENSP00000441445.1:p.Thr201Pro
ENST00000537245.6:c.505A>C ENSP00000439625.2:p.Thr169Pro
ENST00000673471.2:c.691A>C ENSP00000500749.1:p.Thr231Pro
ENST00000674790.1:c.*606A>C ENSP00000502815.1:n.*606A>C
ENST00000675123.1:c.394A>C ENSP00000502132.1:p.Thr132Pro
ENST00000675548.1:c.*222A>C ENSP00000502684.1:n.*222A>C
ENST00000675694.1:c.394A>C ENSP00000501925.1:p.Thr132Pro
ENST00000676255.1:c.356A>C ENSP00000502459.1:n.356A>C
ENST00000340850.9:c.394A>C ENSP00000344570.5:p.Thr132Pro
ENST00000377725.5:c.394A>C ENSP00000366954.1:p.Thr132Pro
ENST00000377728.7:c.394A>C ENSP00000366957.3:p.Thr132Pro
ENST00000377732.5:c.505A>C ENSP00000366961.1:p.Thr169Pro
ENST00000377740.4:c.625A>C ENSP00000366969.3:p.Thr209Pro
ENST00000377748.5:c.625A>C ENSP00000366977.1:p.Thr209Pro
ENST00000400913.5:c.394A>C ENSP00000383704.1:p.Thr132Pro
ENST00000400915.7:c.562A>C ENSP00000383706.3:p.Thr188Pro
ENST00000489097.5:n.870A>C
ENST00000535355.5:c.601A>C ENSP00000441445.1:p.Thr201Pro
ENST00000537245.5:c.631A>C ENSP00000439625.1:p.Thr211Pro
NM_001042663.1:c.562A>C NP_001036128.1:p.Thr188Pro
NM_001042664.1:c.394A>C NP_001036129.1:p.Thr132Pro
NM_001042665.1:c.394A>C NP_001036130.1:p.Thr132Pro
NM_001265592.1:c.631A>C NP_001252521.1:p.Thr211Pro
NM_001265593.1:c.601A>C NP_001252522.1:p.Thr201Pro
NM_001265594.1:c.394A>C NP_001252523.1:p.Thr132Pro
NM_020631.4:c.394A>C NP_065682.2:p.Thr132Pro
NM_198681.3:c.625A>C NP_941374.2:p.Thr209Pro
NM_001042663.2:c.562A>C NP_001036128.1:p.Thr188Pro
NM_001265594.2:c.394A>C NP_001252523.1:p.Thr132Pro
NM_020631.5:c.394A>C NP_065682.2:p.Thr132Pro
NM_001042663.3:c.505A>C NP_001036128.2:p.Thr169Pro
NM_001265592.2:c.505A>C NP_001252521.2:p.Thr169Pro
NM_020631.6:c.394A>C MANE Select NP_065682.2:p.Thr132Pro
NM_198681.4:c.394A>C NP_941374.3:p.Thr132Pro