Canonical Allele Identifier: CA1151524444
Gene: PLEKHG5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.6470582C= , CM000663.2:g.6470582C= GRCh38
NC_000001.10:g.6530642C= , CM000663.1:g.6530642C= GRCh37
NC_000001.9:g.6453229C= NCBI36
NG_007978.1:g.54428G= , LRG_262:g.54428G=
NG_029910.1:g.614G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000340850.10:c.1604G= ENSP00000344570.5:p.Arg535=
ENST00000377728.8:c.1604G= MANE Select ENSP00000366957.3:p.Arg535=
ENST00000377740.5:c.1604G= ENSP00000366969.4:p.Arg535=
ENST00000377748.6:c.1778G= ENSP00000366977.2:p.Arg593=
ENST00000400913.6:c.1604G= ENSP00000383704.1:p.Arg535=
ENST00000400915.8:c.1715G= ENSP00000383706.4:p.Arg572=
ENST00000489097.6:n.2080G=
ENST00000535355.6:c.1811G= ENSP00000441445.1:p.Arg604=
ENST00000537245.6:c.1715G= ENSP00000439625.2:p.Arg572=
ENST00000673471.2:c.1901G= ENSP00000500749.1:p.Arg634=
ENST00000674790.1:c.*1816G= ENSP00000502815.1:n.*1816G=
ENST00000674943.1:n.266G=
ENST00000675123.1:c.1604G= ENSP00000502132.1:p.Arg535=
ENST00000675548.1:c.*1432G= ENSP00000502684.1:n.*1432G=
ENST00000675694.1:c.1604G= ENSP00000501925.1:p.Arg535=
ENST00000676401.1:n.151G=
ENST00000340850.9:c.1604G= ENSP00000344570.5:p.Arg535=
ENST00000377725.5:c.1604G= ENSP00000366954.1:p.Arg535=
ENST00000377728.7:c.1604G= ENSP00000366957.3:p.Arg535=
ENST00000377732.5:c.1715G= ENSP00000366961.1:p.Arg572=
ENST00000377740.4:c.1835G= ENSP00000366969.3:p.Arg612=
ENST00000377748.5:c.1835G= ENSP00000366977.1:p.Arg612=
ENST00000400913.5:c.1604G= ENSP00000383704.1:p.Arg535=
ENST00000400915.7:c.1772G= ENSP00000383706.3:p.Arg591=
ENST00000487949.4:n.806G=
ENST00000489097.5:n.2080G=
ENST00000535355.5:c.1811G= ENSP00000441445.1:p.Arg604=
ENST00000537245.5:c.1841G= ENSP00000439625.1:p.Arg614=
NM_001042663.1:c.1772G= NP_001036128.1:p.Arg591=
NM_001042664.1:c.1604G= NP_001036129.1:p.Arg535=
NM_001042665.1:c.1604G= NP_001036130.1:p.Arg535=
NM_001265592.1:c.1841G= NP_001252521.1:p.Arg614=
NM_001265593.1:c.1811G= NP_001252522.1:p.Arg604=
NM_001265594.1:c.1604G= NP_001252523.1:p.Arg535=
NM_020631.4:c.1604G= NP_065682.2:p.Arg535=
NM_198681.3:c.1835G= NP_941374.2:p.Arg612=
NM_001042663.2:c.1772G= NP_001036128.1:p.Arg591=
NM_001265594.2:c.1604G= NP_001252523.1:p.Arg535=
NM_020631.5:c.1604G= NP_065682.2:p.Arg535=
NM_001042663.3:c.1715G= NP_001036128.2:p.Arg572=
NM_001265592.2:c.1715G= NP_001252521.2:p.Arg572=
NM_020631.6:c.1604G= MANE Select NP_065682.2:p.Arg535=
NM_198681.4:c.1604G= NP_941374.3:p.Arg535=