Canonical Allele Identifier: CA1149110544
Gene: PLEKHG5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.6474153G= , CM000663.2:g.6474153G= GRCh38
NC_000001.10:g.6534213G= , CM000663.1:g.6534213G= GRCh37
NC_000001.9:g.6456800G= NCBI36
NG_007978.1:g.50857C= , LRG_262:g.50857C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000340850.10:c.451C= ENSP00000344570.5:p.Pro151=
ENST00000377728.8:c.451C= MANE Select ENSP00000366957.3:p.Pro151=
ENST00000377740.5:c.451C= ENSP00000366969.4:p.Pro151=
ENST00000377748.6:c.625C= ENSP00000366977.2:p.Pro209=
ENST00000400913.6:c.451C= ENSP00000383704.1:p.Pro151=
ENST00000400915.8:c.562C= ENSP00000383706.4:p.Pro188=
ENST00000489097.6:n.927C=
ENST00000535355.6:c.658C= ENSP00000441445.1:p.Pro220=
ENST00000537245.6:c.562C= ENSP00000439625.2:p.Pro188=
ENST00000673471.2:c.748C= ENSP00000500749.1:p.Pro250=
ENST00000674790.1:c.*663C= ENSP00000502815.1:n.*663C=
ENST00000675123.1:c.451C= ENSP00000502132.1:p.Pro151=
ENST00000675548.1:c.*279C= ENSP00000502684.1:n.*279C=
ENST00000675694.1:c.451C= ENSP00000501925.1:p.Pro151=
ENST00000340850.9:c.451C= ENSP00000344570.5:p.Pro151=
ENST00000377725.5:c.451C= ENSP00000366954.1:p.Pro151=
ENST00000377728.7:c.451C= ENSP00000366957.3:p.Pro151=
ENST00000377732.5:c.562C= ENSP00000366961.1:p.Pro188=
ENST00000377740.4:c.682C= ENSP00000366969.3:p.Pro228=
ENST00000377748.5:c.682C= ENSP00000366977.1:p.Pro228=
ENST00000400913.5:c.451C= ENSP00000383704.1:p.Pro151=
ENST00000400915.7:c.619C= ENSP00000383706.3:p.Pro207=
ENST00000489097.5:n.927C=
ENST00000535355.5:c.658C= ENSP00000441445.1:p.Pro220=
ENST00000537245.5:c.688C= ENSP00000439625.1:p.Pro230=
NM_001042663.1:c.619C= NP_001036128.1:p.Pro207=
NM_001042664.1:c.451C= NP_001036129.1:p.Pro151=
NM_001042665.1:c.451C= NP_001036130.1:p.Pro151=
NM_001265592.1:c.688C= NP_001252521.1:p.Pro230=
NM_001265593.1:c.658C= NP_001252522.1:p.Pro220=
NM_001265594.1:c.451C= NP_001252523.1:p.Pro151=
NM_020631.4:c.451C= NP_065682.2:p.Pro151=
NM_198681.3:c.682C= NP_941374.2:p.Pro228=
NM_001042663.2:c.619C= NP_001036128.1:p.Pro207=
NM_001265594.2:c.451C= NP_001252523.1:p.Pro151=
NM_020631.5:c.451C= NP_065682.2:p.Pro151=
NM_001042663.3:c.562C= NP_001036128.2:p.Pro188=
NM_001265592.2:c.562C= NP_001252521.2:p.Pro188=
NM_020631.6:c.451C= MANE Select NP_065682.2:p.Pro151=
NM_198681.4:c.451C= NP_941374.3:p.Pro151=