Canonical Allele Identifier: CA1151525825

Gene: PLEKHG5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6470872G= , CM000663.2:g.6470872G=	GRCh38
NC_000001.10:g.6530932G= , CM000663.1:g.6530932G=	GRCh37
NC_000001.9:g.6453519G=	NCBI36
NG_007978.1:g.54138C= , LRG_262:g.54138C=
NG_029910.1:g.324C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.1405C=	ENSP00000344570.5:p.His469=
ENST00000377728.8:c.1405C= MANE Select	ENSP00000366957.3:p.His469=
ENST00000377740.5:c.1405C=	ENSP00000366969.4:p.His469=
ENST00000377748.6:c.1579C=	ENSP00000366977.2:p.His527=
ENST00000400913.6:c.1405C=	ENSP00000383704.1:p.His469=
ENST00000400915.8:c.1516C=	ENSP00000383706.4:p.His506=
ENST00000489097.6:n.1881C=
ENST00000535355.6:c.1612C=	ENSP00000441445.1:p.His538=
ENST00000537245.6:c.1516C=	ENSP00000439625.2:p.His506=
ENST00000673471.2:c.1702C=	ENSP00000500749.1:p.His568=
ENST00000674685.1:n.438C=
ENST00000674790.1:c.*1617C=	ENSP00000502815.1:n.*1617C=
ENST00000674943.1:n.67C=
ENST00000675123.1:c.1405C=	ENSP00000502132.1:p.His469=
ENST00000675548.1:c.*1233C=	ENSP00000502684.1:n.*1233C=
ENST00000675694.1:c.1405C=	ENSP00000501925.1:p.His469=
ENST00000340850.9:c.1405C=	ENSP00000344570.5:p.His469=
ENST00000377725.5:c.1405C=	ENSP00000366954.1:p.His469=
ENST00000377728.7:c.1405C=	ENSP00000366957.3:p.His469=
ENST00000377732.5:c.1516C=	ENSP00000366961.1:p.His506=
ENST00000377740.4:c.1636C=	ENSP00000366969.3:p.His546=
ENST00000377748.5:c.1636C=	ENSP00000366977.1:p.His546=
ENST00000400913.5:c.1405C=	ENSP00000383704.1:p.His469=
ENST00000400915.7:c.1573C=	ENSP00000383706.3:p.His525=
ENST00000487949.4:n.607C=
ENST00000489097.5:n.1881C=
ENST00000535355.5:c.1612C=	ENSP00000441445.1:p.His538=
ENST00000537245.5:c.1642C=	ENSP00000439625.1:p.His548=
NM_001042663.1:c.1573C=	NP_001036128.1:p.His525=
NM_001042664.1:c.1405C=	NP_001036129.1:p.His469=
NM_001042665.1:c.1405C=	NP_001036130.1:p.His469=
NM_001265592.1:c.1642C=	NP_001252521.1:p.His548=
NM_001265593.1:c.1612C=	NP_001252522.1:p.His538=
NM_001265594.1:c.1405C=	NP_001252523.1:p.His469=
NM_020631.4:c.1405C=	NP_065682.2:p.His469=
NM_198681.3:c.1636C=	NP_941374.2:p.His546=
NM_001042663.2:c.1573C=	NP_001036128.1:p.His525=
NM_001265594.2:c.1405C=	NP_001252523.1:p.His469=
NM_020631.5:c.1405C=	NP_065682.2:p.His469=
NM_001042663.3:c.1516C=	NP_001036128.2:p.His506=
NM_001265592.2:c.1516C=	NP_001252521.2:p.His506=
NM_020631.6:c.1405C= MANE Select	NP_065682.2:p.His469=
NM_198681.4:c.1405C=	NP_941374.3:p.His469=