Canonical Allele Identifier: CA1151520837

Gene: PLEKHG5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6469231T= , CM000663.2:g.6469231T=	GRCh38
NC_000001.10:g.6529291T= , CM000663.1:g.6529291T=	GRCh37
NC_000001.9:g.6451878T=	NCBI36
NG_007978.1:g.55779A= , LRG_262:g.55779A=
NG_029910.1:g.1965A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.2060A=	ENSP00000344570.5:p.Gln687=
ENST00000377728.8:c.2060A= MANE Select	ENSP00000366957.3:p.Gln687=
ENST00000377740.5:c.2060A=	ENSP00000366969.4:p.Gln687=
ENST00000377748.6:c.2234A=	ENSP00000366977.2:p.Gln745=
ENST00000400913.6:c.2060A=	ENSP00000383704.1:p.Gln687=
ENST00000400915.8:c.2171A=	ENSP00000383706.4:p.Gln724=
ENST00000489097.6:n.2536A=
ENST00000535355.6:c.2267A=	ENSP00000441445.1:p.Gln756=
ENST00000537245.6:c.2171A=	ENSP00000439625.2:p.Gln724=
ENST00000673471.2:c.2357A=	ENSP00000500749.1:p.Gln786=
ENST00000674790.1:c.*2272A=	ENSP00000502815.1:n.*2272A=
ENST00000675123.1:c.2060A=	ENSP00000502132.1:p.Gln687=
ENST00000675139.1:n.131A=
ENST00000675548.1:c.*1888A=	ENSP00000502684.1:n.*1888A=
ENST00000675694.1:c.2060A=	ENSP00000501925.1:p.Gln687=
ENST00000676401.1:n.607A=
ENST00000340850.9:c.2060A=	ENSP00000344570.5:p.Gln687=
ENST00000377725.5:c.2060A=	ENSP00000366954.1:p.Gln687=
ENST00000377728.7:c.2060A=	ENSP00000366957.3:p.Gln687=
ENST00000377732.5:c.2171A=	ENSP00000366961.1:p.Gln724=
ENST00000377740.4:c.2291A=	ENSP00000366969.3:p.Gln764=
ENST00000377748.5:c.2291A=	ENSP00000366977.1:p.Gln764=
ENST00000400913.5:c.2060A=	ENSP00000383704.1:p.Gln687=
ENST00000400915.7:c.2228A=	ENSP00000383706.3:p.Gln743=
ENST00000487949.4:n.1262A=
ENST00000489097.5:n.2536A=
ENST00000535355.5:c.2267A=	ENSP00000441445.1:p.Gln756=
ENST00000537245.5:c.2297A=	ENSP00000439625.1:p.Gln766=
NM_001042663.1:c.2228A=	NP_001036128.1:p.Gln743=
NM_001042664.1:c.2060A=	NP_001036129.1:p.Gln687=
NM_001042665.1:c.2060A=	NP_001036130.1:p.Gln687=
NM_001265592.1:c.2297A=	NP_001252521.1:p.Gln766=
NM_001265593.1:c.2267A=	NP_001252522.1:p.Gln756=
NM_001265594.1:c.2060A=	NP_001252523.1:p.Gln687=
NM_020631.4:c.2060A=	NP_065682.2:p.Gln687=
NM_198681.3:c.2291A=	NP_941374.2:p.Gln764=
NM_001042663.2:c.2228A=	NP_001036128.1:p.Gln743=
NM_001265594.2:c.2060A=	NP_001252523.1:p.Gln687=
NM_020631.5:c.2060A=	NP_065682.2:p.Gln687=
NM_001042663.3:c.2171A=	NP_001036128.2:p.Gln724=
NM_001265592.2:c.2171A=	NP_001252521.2:p.Gln724=
NM_020631.6:c.2060A= MANE Select	NP_065682.2:p.Gln687=
NM_198681.4:c.2060A=	NP_941374.3:p.Gln687=