Canonical Allele Identifier: CA338138472
Gene: PLEKHG5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.6474041T>G , CM000663.2:g.6474041T>G GRCh38
NC_000001.10:g.6534101T>G , CM000663.1:g.6534101T>G GRCh37
NC_000001.9:g.6456688T>G NCBI36
NG_007978.1:g.50969A>C , LRG_262:g.50969A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000340850.10:c.563A>C ENSP00000344570.5:p.Gln188Pro
ENST00000377728.8:c.563A>C MANE Select ENSP00000366957.3:p.Gln188Pro
ENST00000377740.5:c.563A>C ENSP00000366969.4:p.Gln188Pro
ENST00000377748.6:c.737A>C ENSP00000366977.2:p.Gln246Pro
ENST00000400913.6:c.563A>C ENSP00000383704.1:p.Gln188Pro
ENST00000400915.8:c.674A>C ENSP00000383706.4:p.Gln225Pro
ENST00000489097.6:n.1039A>C
ENST00000535355.6:c.770A>C ENSP00000441445.1:p.Gln257Pro
ENST00000537245.6:c.674A>C ENSP00000439625.2:p.Gln225Pro
ENST00000673471.2:c.860A>C ENSP00000500749.1:p.Gln287Pro
ENST00000674790.1:c.*775A>C ENSP00000502815.1:n.*775A>C
ENST00000675123.1:c.563A>C ENSP00000502132.1:p.Gln188Pro
ENST00000675548.1:c.*391A>C ENSP00000502684.1:n.*391A>C
ENST00000675694.1:c.563A>C ENSP00000501925.1:p.Gln188Pro
ENST00000340850.9:c.563A>C ENSP00000344570.5:p.Gln188Pro
ENST00000377725.5:c.563A>C ENSP00000366954.1:p.Gln188Pro
ENST00000377728.7:c.563A>C ENSP00000366957.3:p.Gln188Pro
ENST00000377732.5:c.674A>C ENSP00000366961.1:p.Gln225Pro
ENST00000377740.4:c.794A>C ENSP00000366969.3:p.Gln265Pro
ENST00000377748.5:c.794A>C ENSP00000366977.1:p.Gln265Pro
ENST00000400913.5:c.563A>C ENSP00000383704.1:p.Gln188Pro
ENST00000400915.7:c.731A>C ENSP00000383706.3:p.Gln244Pro
ENST00000489097.5:n.1039A>C
ENST00000535355.5:c.770A>C ENSP00000441445.1:p.Gln257Pro
ENST00000537245.5:c.800A>C ENSP00000439625.1:p.Gln267Pro
NM_001042663.1:c.731A>C NP_001036128.1:p.Gln244Pro
NM_001042664.1:c.563A>C NP_001036129.1:p.Gln188Pro
NM_001042665.1:c.563A>C NP_001036130.1:p.Gln188Pro
NM_001265592.1:c.800A>C NP_001252521.1:p.Gln267Pro
NM_001265593.1:c.770A>C NP_001252522.1:p.Gln257Pro
NM_001265594.1:c.563A>C NP_001252523.1:p.Gln188Pro
NM_020631.4:c.563A>C NP_065682.2:p.Gln188Pro
NM_198681.3:c.794A>C NP_941374.2:p.Gln265Pro
NM_001042663.2:c.731A>C NP_001036128.1:p.Gln244Pro
NM_001265594.2:c.563A>C NP_001252523.1:p.Gln188Pro
NM_020631.5:c.563A>C NP_065682.2:p.Gln188Pro
NM_001042663.3:c.674A>C NP_001036128.2:p.Gln225Pro
NM_001265592.2:c.674A>C NP_001252521.2:p.Gln225Pro
NM_020631.6:c.563A>C MANE Select NP_065682.2:p.Gln188Pro
NM_198681.4:c.563A>C NP_941374.3:p.Gln188Pro