Canonical Allele Identifier: CA1151520150

Gene: PLEKHG5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6469111C= , CM000663.2:g.6469111C=	GRCh38
NC_000001.10:g.6529171C= , CM000663.1:g.6529171C=	GRCh37
NC_000001.9:g.6451758C=	NCBI36
NG_007978.1:g.55899G= , LRG_262:g.55899G=
NG_029910.1:g.2085G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.2180G=	ENSP00000344570.5:p.Ser727=
ENST00000377728.8:c.2180G= MANE Select	ENSP00000366957.3:p.Ser727=
ENST00000377740.5:c.2180G=	ENSP00000366969.4:p.Ser727=
ENST00000377748.6:c.2354G=	ENSP00000366977.2:p.Ser785=
ENST00000400913.6:c.2180G=	ENSP00000383704.1:p.Ser727=
ENST00000400915.8:c.2291G=	ENSP00000383706.4:p.Ser764=
ENST00000489097.6:n.2656G=
ENST00000535355.6:c.2387G=	ENSP00000441445.1:p.Ser796=
ENST00000537245.6:c.2291G=	ENSP00000439625.2:p.Ser764=
ENST00000673471.2:c.2477G=	ENSP00000500749.1:p.Ser826=
ENST00000674790.1:c.*2392G=	ENSP00000502815.1:n.*2392G=
ENST00000675123.1:c.2180G=	ENSP00000502132.1:p.Ser727=
ENST00000675139.1:n.251G=
ENST00000675548.1:c.*2008G=	ENSP00000502684.1:n.*2008G=
ENST00000675694.1:c.2180G=	ENSP00000501925.1:p.Ser727=
ENST00000675976.1:c.53G=	ENSP00000501611.1:p.Ser18=
ENST00000340850.9:c.2180G=	ENSP00000344570.5:p.Ser727=
ENST00000377725.5:c.2180G=	ENSP00000366954.1:p.Ser727=
ENST00000377728.7:c.2180G=	ENSP00000366957.3:p.Ser727=
ENST00000377732.5:c.2291G=	ENSP00000366961.1:p.Ser764=
ENST00000377740.4:c.2411G=	ENSP00000366969.3:p.Ser804=
ENST00000377748.5:c.2411G=	ENSP00000366977.1:p.Ser804=
ENST00000400913.5:c.2180G=	ENSP00000383704.1:p.Ser727=
ENST00000400915.7:c.2348G=	ENSP00000383706.3:p.Ser783=
ENST00000487949.4:n.1382G=
ENST00000489097.5:n.2656G=
ENST00000535355.5:c.2387G=	ENSP00000441445.1:p.Ser796=
ENST00000537245.5:c.2417G=	ENSP00000439625.1:p.Ser806=
NM_001042663.1:c.2348G=	NP_001036128.1:p.Ser783=
NM_001042664.1:c.2180G=	NP_001036129.1:p.Ser727=
NM_001042665.1:c.2180G=	NP_001036130.1:p.Ser727=
NM_001265592.1:c.2417G=	NP_001252521.1:p.Ser806=
NM_001265593.1:c.2387G=	NP_001252522.1:p.Ser796=
NM_001265594.1:c.2180G=	NP_001252523.1:p.Ser727=
NM_020631.4:c.2180G=	NP_065682.2:p.Ser727=
NM_198681.3:c.2411G=	NP_941374.2:p.Ser804=
NM_001042663.2:c.2348G=	NP_001036128.1:p.Ser783=
NM_001265594.2:c.2180G=	NP_001252523.1:p.Ser727=
NM_020631.5:c.2180G=	NP_065682.2:p.Ser727=
NM_001042663.3:c.2291G=	NP_001036128.2:p.Ser764=
NM_001265592.2:c.2291G=	NP_001252521.2:p.Ser764=
NM_020631.6:c.2180G= MANE Select	NP_065682.2:p.Ser727=
NM_198681.4:c.2180G=	NP_941374.3:p.Ser727=