Canonical Allele Identifier: CA1151525737

Gene: PLEKHG5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6470850T= , CM000663.2:g.6470850T=	GRCh38
NC_000001.10:g.6530910T= , CM000663.1:g.6530910T=	GRCh37
NC_000001.9:g.6453497T=	NCBI36
NG_007978.1:g.54160A= , LRG_262:g.54160A=
NG_029910.1:g.346A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.1427A=	ENSP00000344570.5:p.Lys476=
ENST00000377728.8:c.1427A= MANE Select	ENSP00000366957.3:p.Lys476=
ENST00000377740.5:c.1427A=	ENSP00000366969.4:p.Lys476=
ENST00000377748.6:c.1601A=	ENSP00000366977.2:p.Lys534=
ENST00000400913.6:c.1427A=	ENSP00000383704.1:p.Lys476=
ENST00000400915.8:c.1538A=	ENSP00000383706.4:p.Lys513=
ENST00000489097.6:n.1903A=
ENST00000535355.6:c.1634A=	ENSP00000441445.1:p.Lys545=
ENST00000537245.6:c.1538A=	ENSP00000439625.2:p.Lys513=
ENST00000673471.2:c.1724A=	ENSP00000500749.1:p.Lys575=
ENST00000674685.1:n.460A=
ENST00000674790.1:c.*1639A=	ENSP00000502815.1:n.*1639A=
ENST00000674943.1:n.89A=
ENST00000675123.1:c.1427A=	ENSP00000502132.1:p.Lys476=
ENST00000675548.1:c.*1255A=	ENSP00000502684.1:n.*1255A=
ENST00000675694.1:c.1427A=	ENSP00000501925.1:p.Lys476=
ENST00000340850.9:c.1427A=	ENSP00000344570.5:p.Lys476=
ENST00000377725.5:c.1427A=	ENSP00000366954.1:p.Lys476=
ENST00000377728.7:c.1427A=	ENSP00000366957.3:p.Lys476=
ENST00000377732.5:c.1538A=	ENSP00000366961.1:p.Lys513=
ENST00000377740.4:c.1658A=	ENSP00000366969.3:p.Lys553=
ENST00000377748.5:c.1658A=	ENSP00000366977.1:p.Lys553=
ENST00000400913.5:c.1427A=	ENSP00000383704.1:p.Lys476=
ENST00000400915.7:c.1595A=	ENSP00000383706.3:p.Lys532=
ENST00000487949.4:n.629A=
ENST00000489097.5:n.1903A=
ENST00000535355.5:c.1634A=	ENSP00000441445.1:p.Lys545=
ENST00000537245.5:c.1664A=	ENSP00000439625.1:p.Lys555=
NM_001042663.1:c.1595A=	NP_001036128.1:p.Lys532=
NM_001042664.1:c.1427A=	NP_001036129.1:p.Lys476=
NM_001042665.1:c.1427A=	NP_001036130.1:p.Lys476=
NM_001265592.1:c.1664A=	NP_001252521.1:p.Lys555=
NM_001265593.1:c.1634A=	NP_001252522.1:p.Lys545=
NM_001265594.1:c.1427A=	NP_001252523.1:p.Lys476=
NM_020631.4:c.1427A=	NP_065682.2:p.Lys476=
NM_198681.3:c.1658A=	NP_941374.2:p.Lys553=
NM_001042663.2:c.1595A=	NP_001036128.1:p.Lys532=
NM_001265594.2:c.1427A=	NP_001252523.1:p.Lys476=
NM_020631.5:c.1427A=	NP_065682.2:p.Lys476=
NM_001042663.3:c.1538A=	NP_001036128.2:p.Lys513=
NM_001265592.2:c.1538A=	NP_001252521.2:p.Lys513=
NM_020631.6:c.1427A= MANE Select	NP_065682.2:p.Lys476=
NM_198681.4:c.1427A=	NP_941374.3:p.Lys476=