Canonical Allele Identifier: CA1151526372

Gene: PLEKHG5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6470982G= , CM000663.2:g.6470982G=	GRCh38
NC_000001.10:g.6531042G= , CM000663.1:g.6531042G=	GRCh37
NC_000001.9:g.6453629G=	NCBI36
NG_007978.1:g.54028C= , LRG_262:g.54028C=
NG_029910.1:g.214C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.1392+8C=	ENSP00000344570.5:n.1392+8C=
ENST00000377728.8:c.1392+8C= MANE Select	ENSP00000366957.3:n.1392+8C=
ENST00000377740.5:c.1392+8C=	ENSP00000366969.4:n.1392+8C=
ENST00000377748.6:c.1566+8C=	ENSP00000366977.2:n.1566+8C=
ENST00000400913.6:c.1392+8C=	ENSP00000383704.1:n.1392+8C=
ENST00000400915.8:c.1503+8C=	ENSP00000383706.4:n.1503+8C=
ENST00000489097.6:n.1868+8C=
ENST00000535355.6:c.1599+8C=	ENSP00000441445.1:n.1599+8C=
ENST00000537245.6:c.1503+8C=	ENSP00000439625.2:n.1503+8C=
ENST00000673471.2:c.1689+8C=	ENSP00000500749.1:n.1689+8C=
ENST00000674685.1:n.425+8C=
ENST00000674790.1:c.*1604+8C=	ENSP00000502815.1:n.*1604+8C=
ENST00000675123.1:c.1392+8C=	ENSP00000502132.1:n.1392+8C=
ENST00000675548.1:c.*1220+8C=	ENSP00000502684.1:n.*1220+8C=
ENST00000675694.1:c.1392+8C=	ENSP00000501925.1:n.1392+8C=
ENST00000340850.9:c.1392+8C=	ENSP00000344570.5:n.1392+8C=
ENST00000377725.5:c.1392+8C=	ENSP00000366954.1:n.1392+8C=
ENST00000377728.7:c.1392+8C=	ENSP00000366957.3:n.1392+8C=
ENST00000377732.5:c.1503+8C=	ENSP00000366961.1:n.1503+8C=
ENST00000377740.4:c.1623+8C=	ENSP00000366969.3:n.1623+8C=
ENST00000377748.5:c.1623+8C=	ENSP00000366977.1:n.1623+8C=
ENST00000400913.5:c.1392+8C=	ENSP00000383704.1:n.1392+8C=
ENST00000400915.7:c.1560+8C=	ENSP00000383706.3:n.1560+8C=
ENST00000487949.4:n.594+8C=
ENST00000489097.5:n.1868+8C=
ENST00000535355.5:c.1599+8C=	ENSP00000441445.1:n.1599+8C=
ENST00000537245.5:c.1629+8C=	ENSP00000439625.1:n.1629+8C=
NM_001042663.1:c.1560+8C=	NP_001036128.1:n.1560+8C=
NM_001042664.1:c.1392+8C=	NP_001036129.1:n.1392+8C=
NM_001042665.1:c.1392+8C=	NP_001036130.1:n.1392+8C=
NM_001265592.1:c.1629+8C=	NP_001252521.1:n.1629+8C=
NM_001265593.1:c.1599+8C=	NP_001252522.1:n.1599+8C=
NM_001265594.1:c.1392+8C=	NP_001252523.1:n.1392+8C=
NM_020631.4:c.1392+8C=	NP_065682.2:n.1392+8C=
NM_198681.3:c.1623+8C=	NP_941374.2:n.1623+8C=
NM_001042663.2:c.1560+8C=	NP_001036128.1:n.1560+8C=
NM_001265594.2:c.1392+8C=	NP_001252523.1:n.1392+8C=
NM_020631.5:c.1392+8C=	NP_065682.2:n.1392+8C=
NM_001042663.3:c.1503+8C=	NP_001036128.2:n.1503+8C=
NM_001265592.2:c.1503+8C=	NP_001252521.2:n.1503+8C=
NM_020631.6:c.1392+8C= MANE Select	NP_065682.2:n.1392+8C=
NM_198681.4:c.1392+8C=	NP_941374.3:n.1392+8C=