Canonical Allele Identifier: CA1151525551

Gene: PLEKHG5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6470806A= , CM000663.2:g.6470806A=	GRCh38
NC_000001.10:g.6530866A= , CM000663.1:g.6530866A=	GRCh37
NC_000001.9:g.6453453A=	NCBI36
NG_007978.1:g.54204T= , LRG_262:g.54204T=
NG_029910.1:g.390T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.1471T=	ENSP00000344570.5:p.Tyr491=
ENST00000377728.8:c.1471T= MANE Select	ENSP00000366957.3:p.Tyr491=
ENST00000377740.5:c.1471T=	ENSP00000366969.4:p.Tyr491=
ENST00000377748.6:c.1645T=	ENSP00000366977.2:p.Tyr549=
ENST00000400913.6:c.1471T=	ENSP00000383704.1:p.Tyr491=
ENST00000400915.8:c.1582T=	ENSP00000383706.4:p.Tyr528=
ENST00000489097.6:n.1947T=
ENST00000535355.6:c.1678T=	ENSP00000441445.1:p.Tyr560=
ENST00000537245.6:c.1582T=	ENSP00000439625.2:p.Tyr528=
ENST00000673471.2:c.1768T=	ENSP00000500749.1:p.Tyr590=
ENST00000674685.1:n.504T=
ENST00000674790.1:c.*1683T=	ENSP00000502815.1:n.*1683T=
ENST00000674943.1:n.133T=
ENST00000675123.1:c.1471T=	ENSP00000502132.1:p.Tyr491=
ENST00000675548.1:c.*1299T=	ENSP00000502684.1:n.*1299T=
ENST00000675694.1:c.1471T=	ENSP00000501925.1:p.Tyr491=
ENST00000340850.9:c.1471T=	ENSP00000344570.5:p.Tyr491=
ENST00000377725.5:c.1471T=	ENSP00000366954.1:p.Tyr491=
ENST00000377728.7:c.1471T=	ENSP00000366957.3:p.Tyr491=
ENST00000377732.5:c.1582T=	ENSP00000366961.1:p.Tyr528=
ENST00000377740.4:c.1702T=	ENSP00000366969.3:p.Tyr568=
ENST00000377748.5:c.1702T=	ENSP00000366977.1:p.Tyr568=
ENST00000400913.5:c.1471T=	ENSP00000383704.1:p.Tyr491=
ENST00000400915.7:c.1639T=	ENSP00000383706.3:p.Tyr547=
ENST00000487949.4:n.673T=
ENST00000489097.5:n.1947T=
ENST00000535355.5:c.1678T=	ENSP00000441445.1:p.Tyr560=
ENST00000537245.5:c.1708T=	ENSP00000439625.1:p.Tyr570=
NM_001042663.1:c.1639T=	NP_001036128.1:p.Tyr547=
NM_001042664.1:c.1471T=	NP_001036129.1:p.Tyr491=
NM_001042665.1:c.1471T=	NP_001036130.1:p.Tyr491=
NM_001265592.1:c.1708T=	NP_001252521.1:p.Tyr570=
NM_001265593.1:c.1678T=	NP_001252522.1:p.Tyr560=
NM_001265594.1:c.1471T=	NP_001252523.1:p.Tyr491=
NM_020631.4:c.1471T=	NP_065682.2:p.Tyr491=
NM_198681.3:c.1702T=	NP_941374.2:p.Tyr568=
NM_001042663.2:c.1639T=	NP_001036128.1:p.Tyr547=
NM_001265594.2:c.1471T=	NP_001252523.1:p.Tyr491=
NM_020631.5:c.1471T=	NP_065682.2:p.Tyr491=
NM_001042663.3:c.1582T=	NP_001036128.2:p.Tyr528=
NM_001265592.2:c.1582T=	NP_001252521.2:p.Tyr528=
NM_020631.6:c.1471T= MANE Select	NP_065682.2:p.Tyr491=
NM_198681.4:c.1471T=	NP_941374.3:p.Tyr491=