Canonical Allele Identifier: CA338138871
Gene: PLEKHG5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.6474140C>G , CM000663.2:g.6474140C>G GRCh38
NC_000001.10:g.6534200C>G , CM000663.1:g.6534200C>G GRCh37
NC_000001.9:g.6456787C>G NCBI36
NG_007978.1:g.50870G>C , LRG_262:g.50870G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000340850.10:c.464G>C ENSP00000344570.5:p.Gly155Ala
ENST00000377728.8:c.464G>C MANE Select ENSP00000366957.3:p.Gly155Ala
ENST00000377740.5:c.464G>C ENSP00000366969.4:p.Gly155Ala
ENST00000377748.6:c.638G>C ENSP00000366977.2:p.Gly213Ala
ENST00000400913.6:c.464G>C ENSP00000383704.1:p.Gly155Ala
ENST00000400915.8:c.575G>C ENSP00000383706.4:p.Gly192Ala
ENST00000489097.6:n.940G>C
ENST00000535355.6:c.671G>C ENSP00000441445.1:p.Gly224Ala
ENST00000537245.6:c.575G>C ENSP00000439625.2:p.Gly192Ala
ENST00000673471.2:c.761G>C ENSP00000500749.1:p.Gly254Ala
ENST00000674790.1:c.*676G>C ENSP00000502815.1:n.*676G>C
ENST00000675123.1:c.464G>C ENSP00000502132.1:p.Gly155Ala
ENST00000675548.1:c.*292G>C ENSP00000502684.1:n.*292G>C
ENST00000675694.1:c.464G>C ENSP00000501925.1:p.Gly155Ala
ENST00000340850.9:c.464G>C ENSP00000344570.5:p.Gly155Ala
ENST00000377725.5:c.464G>C ENSP00000366954.1:p.Gly155Ala
ENST00000377728.7:c.464G>C ENSP00000366957.3:p.Gly155Ala
ENST00000377732.5:c.575G>C ENSP00000366961.1:p.Gly192Ala
ENST00000377740.4:c.695G>C ENSP00000366969.3:p.Gly232Ala
ENST00000377748.5:c.695G>C ENSP00000366977.1:p.Gly232Ala
ENST00000400913.5:c.464G>C ENSP00000383704.1:p.Gly155Ala
ENST00000400915.7:c.632G>C ENSP00000383706.3:p.Gly211Ala
ENST00000489097.5:n.940G>C
ENST00000535355.5:c.671G>C ENSP00000441445.1:p.Gly224Ala
ENST00000537245.5:c.701G>C ENSP00000439625.1:p.Gly234Ala
NM_001042663.1:c.632G>C NP_001036128.1:p.Gly211Ala
NM_001042664.1:c.464G>C NP_001036129.1:p.Gly155Ala
NM_001042665.1:c.464G>C NP_001036130.1:p.Gly155Ala
NM_001265592.1:c.701G>C NP_001252521.1:p.Gly234Ala
NM_001265593.1:c.671G>C NP_001252522.1:p.Gly224Ala
NM_001265594.1:c.464G>C NP_001252523.1:p.Gly155Ala
NM_020631.4:c.464G>C NP_065682.2:p.Gly155Ala
NM_198681.3:c.695G>C NP_941374.2:p.Gly232Ala
NM_001042663.2:c.632G>C NP_001036128.1:p.Gly211Ala
NM_001265594.2:c.464G>C NP_001252523.1:p.Gly155Ala
NM_020631.5:c.464G>C NP_065682.2:p.Gly155Ala
NM_001042663.3:c.575G>C NP_001036128.2:p.Gly192Ala
NM_001265592.2:c.575G>C NP_001252521.2:p.Gly192Ala
NM_020631.6:c.464G>C MANE Select NP_065682.2:p.Gly155Ala
NM_198681.4:c.464G>C NP_941374.3:p.Gly155Ala