Canonical Allele Identifier: CA338142099
Gene: PLEKHG5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.6477570A>T , CM000663.2:g.6477570A>T GRCh38
NC_000001.10:g.6537630A>T , CM000663.1:g.6537630A>T GRCh37
NC_000001.9:g.6460217A>T NCBI36
NG_007978.1:g.47440T>A , LRG_262:g.47440T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000340850.10:c.2T>A ENSP00000344570.5:p.Met1Lys
ENST00000377728.8:c.2T>A MANE Select ENSP00000366957.3:p.Met1Lys
ENST00000377740.5:c.2T>A ENSP00000366969.4:p.Met1Lys
ENST00000377748.6:c.113T>A ENSP00000366977.2:p.Met38Lys
ENST00000400913.6:c.2T>A ENSP00000383704.1:p.Met1Lys
ENST00000400915.8:c.113T>A ENSP00000383706.4:p.Met38Lys
ENST00000489097.6:n.19T>A
ENST00000535355.6:c.209T>A ENSP00000441445.1:p.Met70Lys
ENST00000537245.6:c.113T>A ENSP00000439625.2:p.Met38Lys
ENST00000673471.2:c.299T>A ENSP00000500749.1:p.Met100Lys
ENST00000674790.1:c.*214T>A ENSP00000502815.1:n.*214T>A
ENST00000674803.1:n.232T>A
ENST00000675093.1:c.2T>A ENSP00000502687.1:p.Met1Lys
ENST00000675123.1:c.2T>A ENSP00000502132.1:p.Met1Lys
ENST00000675548.1:c.187T>A ENSP00000502684.1:p.Cys63Ser
ENST00000675655.1:n.208T>A
ENST00000675694.1:c.2T>A ENSP00000501925.1:p.Met1Lys
ENST00000676287.1:c.2T>A ENSP00000502810.1:p.Met1Lys
ENST00000676362.1:n.225T>A
ENST00000340850.9:c.2T>A ENSP00000344570.5:p.Met1Lys
ENST00000377725.5:c.2T>A ENSP00000366954.1:p.Met1Lys
ENST00000377728.7:c.2T>A ENSP00000366957.3:p.Met1Lys
ENST00000377732.5:c.113T>A ENSP00000366961.1:p.Met38Lys
ENST00000377740.4:c.233T>A ENSP00000366969.3:p.Met78Lys
ENST00000377748.5:c.233T>A ENSP00000366977.1:p.Met78Lys
ENST00000400913.5:c.2T>A ENSP00000383704.1:p.Met1Lys
ENST00000400915.7:c.170T>A ENSP00000383706.3:p.Met57Lys
ENST00000489097.5:n.19T>A
ENST00000535355.5:c.209T>A ENSP00000441445.1:p.Met70Lys
ENST00000537245.5:c.239T>A ENSP00000439625.1:p.Met80Lys
NM_001042663.1:c.170T>A NP_001036128.1:p.Met57Lys
NM_001042664.1:c.2T>A NP_001036129.1:p.Met1Lys
NM_001042665.1:c.2T>A NP_001036130.1:p.Met1Lys
NM_001265592.1:c.239T>A NP_001252521.1:p.Met80Lys
NM_001265593.1:c.209T>A NP_001252522.1:p.Met70Lys
NM_001265594.1:c.2T>A NP_001252523.1:p.Met1Lys
NM_020631.4:c.2T>A NP_065682.2:p.Met1Lys
NM_198681.3:c.233T>A NP_941374.2:p.Met78Lys
NM_001042663.2:c.170T>A NP_001036128.1:p.Met57Lys
NM_001265594.2:c.2T>A NP_001252523.1:p.Met1Lys
NM_020631.5:c.2T>A NP_065682.2:p.Met1Lys
NM_001042663.3:c.113T>A NP_001036128.2:p.Met38Lys
NM_001265592.2:c.113T>A NP_001252521.2:p.Met38Lys
NM_020631.6:c.2T>A MANE Select NP_065682.2:p.Met1Lys
NM_198681.4:c.2T>A NP_941374.3:p.Met1Lys