Canonical Allele Identifier: CA1151524492
Gene: PLEKHG5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.6470595G= , CM000663.2:g.6470595G= GRCh38
NC_000001.10:g.6530655G= , CM000663.1:g.6530655G= GRCh37
NC_000001.9:g.6453242G= NCBI36
NG_007978.1:g.54415C= , LRG_262:g.54415C=
NG_029910.1:g.601C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000340850.10:c.1591C= ENSP00000344570.5:p.Gln531=
ENST00000377728.8:c.1591C= MANE Select ENSP00000366957.3:p.Gln531=
ENST00000377740.5:c.1591C= ENSP00000366969.4:p.Gln531=
ENST00000377748.6:c.1765C= ENSP00000366977.2:p.Gln589=
ENST00000400913.6:c.1591C= ENSP00000383704.1:p.Gln531=
ENST00000400915.8:c.1702C= ENSP00000383706.4:p.Gln568=
ENST00000489097.6:n.2067C=
ENST00000535355.6:c.1798C= ENSP00000441445.1:p.Gln600=
ENST00000537245.6:c.1702C= ENSP00000439625.2:p.Gln568=
ENST00000673471.2:c.1888C= ENSP00000500749.1:p.Gln630=
ENST00000674790.1:c.*1803C= ENSP00000502815.1:n.*1803C=
ENST00000674943.1:n.253C=
ENST00000675123.1:c.1591C= ENSP00000502132.1:p.Gln531=
ENST00000675548.1:c.*1419C= ENSP00000502684.1:n.*1419C=
ENST00000675694.1:c.1591C= ENSP00000501925.1:p.Gln531=
ENST00000676401.1:n.138C=
ENST00000340850.9:c.1591C= ENSP00000344570.5:p.Gln531=
ENST00000377725.5:c.1591C= ENSP00000366954.1:p.Gln531=
ENST00000377728.7:c.1591C= ENSP00000366957.3:p.Gln531=
ENST00000377732.5:c.1702C= ENSP00000366961.1:p.Gln568=
ENST00000377740.4:c.1822C= ENSP00000366969.3:p.Gln608=
ENST00000377748.5:c.1822C= ENSP00000366977.1:p.Gln608=
ENST00000400913.5:c.1591C= ENSP00000383704.1:p.Gln531=
ENST00000400915.7:c.1759C= ENSP00000383706.3:p.Gln587=
ENST00000487949.4:n.793C=
ENST00000489097.5:n.2067C=
ENST00000535355.5:c.1798C= ENSP00000441445.1:p.Gln600=
ENST00000537245.5:c.1828C= ENSP00000439625.1:p.Gln610=
NM_001042663.1:c.1759C= NP_001036128.1:p.Gln587=
NM_001042664.1:c.1591C= NP_001036129.1:p.Gln531=
NM_001042665.1:c.1591C= NP_001036130.1:p.Gln531=
NM_001265592.1:c.1828C= NP_001252521.1:p.Gln610=
NM_001265593.1:c.1798C= NP_001252522.1:p.Gln600=
NM_001265594.1:c.1591C= NP_001252523.1:p.Gln531=
NM_020631.4:c.1591C= NP_065682.2:p.Gln531=
NM_198681.3:c.1822C= NP_941374.2:p.Gln608=
NM_001042663.2:c.1759C= NP_001036128.1:p.Gln587=
NM_001265594.2:c.1591C= NP_001252523.1:p.Gln531=
NM_020631.5:c.1591C= NP_065682.2:p.Gln531=
NM_001042663.3:c.1702C= NP_001036128.2:p.Gln568=
NM_001265592.2:c.1702C= NP_001252521.2:p.Gln568=
NM_020631.6:c.1591C= MANE Select NP_065682.2:p.Gln531=
NM_198681.4:c.1591C= NP_941374.3:p.Gln531=