Canonical Allele Identifier: CA1151524433
Gene: PLEKHG5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.6470579T= , CM000663.2:g.6470579T= GRCh38
NC_000001.10:g.6530639T= , CM000663.1:g.6530639T= GRCh37
NC_000001.9:g.6453226T= NCBI36
NG_007978.1:g.54431A= , LRG_262:g.54431A=
NG_029910.1:g.617A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000340850.10:c.1607A= ENSP00000344570.5:p.Gln536=
ENST00000377728.8:c.1607A= MANE Select ENSP00000366957.3:p.Gln536=
ENST00000377740.5:c.1607A= ENSP00000366969.4:p.Gln536=
ENST00000377748.6:c.1781A= ENSP00000366977.2:p.Gln594=
ENST00000400913.6:c.1607A= ENSP00000383704.1:p.Gln536=
ENST00000400915.8:c.1718A= ENSP00000383706.4:p.Gln573=
ENST00000489097.6:n.2083A=
ENST00000535355.6:c.1814A= ENSP00000441445.1:p.Gln605=
ENST00000537245.6:c.1718A= ENSP00000439625.2:p.Gln573=
ENST00000673471.2:c.1904A= ENSP00000500749.1:p.Gln635=
ENST00000674790.1:c.*1819A= ENSP00000502815.1:n.*1819A=
ENST00000674943.1:n.269A=
ENST00000675123.1:c.1607A= ENSP00000502132.1:p.Gln536=
ENST00000675548.1:c.*1435A= ENSP00000502684.1:n.*1435A=
ENST00000675694.1:c.1607A= ENSP00000501925.1:p.Gln536=
ENST00000676401.1:n.154A=
ENST00000340850.9:c.1607A= ENSP00000344570.5:p.Gln536=
ENST00000377725.5:c.1607A= ENSP00000366954.1:p.Gln536=
ENST00000377728.7:c.1607A= ENSP00000366957.3:p.Gln536=
ENST00000377732.5:c.1718A= ENSP00000366961.1:p.Gln573=
ENST00000377740.4:c.1838A= ENSP00000366969.3:p.Gln613=
ENST00000377748.5:c.1838A= ENSP00000366977.1:p.Gln613=
ENST00000400913.5:c.1607A= ENSP00000383704.1:p.Gln536=
ENST00000400915.7:c.1775A= ENSP00000383706.3:p.Gln592=
ENST00000487949.4:n.809A=
ENST00000489097.5:n.2083A=
ENST00000535355.5:c.1814A= ENSP00000441445.1:p.Gln605=
ENST00000537245.5:c.1844A= ENSP00000439625.1:p.Gln615=
NM_001042663.1:c.1775A= NP_001036128.1:p.Gln592=
NM_001042664.1:c.1607A= NP_001036129.1:p.Gln536=
NM_001042665.1:c.1607A= NP_001036130.1:p.Gln536=
NM_001265592.1:c.1844A= NP_001252521.1:p.Gln615=
NM_001265593.1:c.1814A= NP_001252522.1:p.Gln605=
NM_001265594.1:c.1607A= NP_001252523.1:p.Gln536=
NM_020631.4:c.1607A= NP_065682.2:p.Gln536=
NM_198681.3:c.1838A= NP_941374.2:p.Gln613=
NM_001042663.2:c.1775A= NP_001036128.1:p.Gln592=
NM_001265594.2:c.1607A= NP_001252523.1:p.Gln536=
NM_020631.5:c.1607A= NP_065682.2:p.Gln536=
NM_001042663.3:c.1718A= NP_001036128.2:p.Gln573=
NM_001265592.2:c.1718A= NP_001252521.2:p.Gln573=
NM_020631.6:c.1607A= MANE Select NP_065682.2:p.Gln536=
NM_198681.4:c.1607A= NP_941374.3:p.Gln536=