Canonical Allele Identifier: CA1151520139

Gene: PLEKHG5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6469105G= , CM000663.2:g.6469105G=	GRCh38
NC_000001.10:g.6529165G= , CM000663.1:g.6529165G=	GRCh37
NC_000001.9:g.6451752G=	NCBI36
NG_007978.1:g.55905C= , LRG_262:g.55905C=
NG_029910.1:g.2091C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.2186C=	ENSP00000344570.5:p.Thr729=
ENST00000377728.8:c.2186C= MANE Select	ENSP00000366957.3:p.Thr729=
ENST00000377740.5:c.2186C=	ENSP00000366969.4:p.Thr729=
ENST00000377748.6:c.2360C=	ENSP00000366977.2:p.Thr787=
ENST00000400913.6:c.2186C=	ENSP00000383704.1:p.Thr729=
ENST00000400915.8:c.2297C=	ENSP00000383706.4:p.Thr766=
ENST00000489097.6:n.2662C=
ENST00000535355.6:c.2393C=	ENSP00000441445.1:p.Thr798=
ENST00000537245.6:c.2297C=	ENSP00000439625.2:p.Thr766=
ENST00000673471.2:c.2483C=	ENSP00000500749.1:p.Thr828=
ENST00000674790.1:c.*2398C=	ENSP00000502815.1:n.*2398C=
ENST00000675123.1:c.2186C=	ENSP00000502132.1:p.Thr729=
ENST00000675139.1:n.257C=
ENST00000675548.1:c.*2014C=	ENSP00000502684.1:n.*2014C=
ENST00000675694.1:c.2186C=	ENSP00000501925.1:p.Thr729=
ENST00000675976.1:c.59C=	ENSP00000501611.1:p.Thr20=
ENST00000340850.9:c.2186C=	ENSP00000344570.5:p.Thr729=
ENST00000377725.5:c.2186C=	ENSP00000366954.1:p.Thr729=
ENST00000377728.7:c.2186C=	ENSP00000366957.3:p.Thr729=
ENST00000377732.5:c.2297C=	ENSP00000366961.1:p.Thr766=
ENST00000377740.4:c.2417C=	ENSP00000366969.3:p.Thr806=
ENST00000377748.5:c.2417C=	ENSP00000366977.1:p.Thr806=
ENST00000400913.5:c.2186C=	ENSP00000383704.1:p.Thr729=
ENST00000400915.7:c.2354C=	ENSP00000383706.3:p.Thr785=
ENST00000487949.4:n.1388C=
ENST00000489097.5:n.2662C=
ENST00000535355.5:c.2393C=	ENSP00000441445.1:p.Thr798=
ENST00000537245.5:c.2423C=	ENSP00000439625.1:p.Thr808=
NM_001042663.1:c.2354C=	NP_001036128.1:p.Thr785=
NM_001042664.1:c.2186C=	NP_001036129.1:p.Thr729=
NM_001042665.1:c.2186C=	NP_001036130.1:p.Thr729=
NM_001265592.1:c.2423C=	NP_001252521.1:p.Thr808=
NM_001265593.1:c.2393C=	NP_001252522.1:p.Thr798=
NM_001265594.1:c.2186C=	NP_001252523.1:p.Thr729=
NM_020631.4:c.2186C=	NP_065682.2:p.Thr729=
NM_198681.3:c.2417C=	NP_941374.2:p.Thr806=
NM_001042663.2:c.2354C=	NP_001036128.1:p.Thr785=
NM_001265594.2:c.2186C=	NP_001252523.1:p.Thr729=
NM_020631.5:c.2186C=	NP_065682.2:p.Thr729=
NM_001042663.3:c.2297C=	NP_001036128.2:p.Thr766=
NM_001265592.2:c.2297C=	NP_001252521.2:p.Thr766=
NM_020631.6:c.2186C= MANE Select	NP_065682.2:p.Thr729=
NM_198681.4:c.2186C=	NP_941374.3:p.Thr729=