Canonical Allele Identifier: CA1151506963

Gene: PLEKHG5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6474502A= , CM000663.2:g.6474502A=	GRCh38
NC_000001.10:g.6534562A= , CM000663.1:g.6534562A=	GRCh37
NC_000001.9:g.6457149A=	NCBI36
NG_007978.1:g.50508T= , LRG_262:g.50508T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.388T=	ENSP00000344570.5:p.Ser130=
ENST00000377728.8:c.388T= MANE Select	ENSP00000366957.3:p.Ser130=
ENST00000377740.5:c.388T=	ENSP00000366969.4:p.Ser130=
ENST00000377748.6:c.562T=	ENSP00000366977.2:p.Ser188=
ENST00000400913.6:c.388T=	ENSP00000383704.1:p.Ser130=
ENST00000400915.8:c.499T=	ENSP00000383706.4:p.Ser167=
ENST00000489097.6:n.864T=
ENST00000535355.6:c.595T=	ENSP00000441445.1:p.Ser199=
ENST00000537245.6:c.499T=	ENSP00000439625.2:p.Ser167=
ENST00000673471.2:c.685T=	ENSP00000500749.1:p.Ser229=
ENST00000674790.1:c.*600T=	ENSP00000502815.1:n.*600T=
ENST00000675123.1:c.388T=	ENSP00000502132.1:p.Ser130=
ENST00000675548.1:c.*216T=	ENSP00000502684.1:n.*216T=
ENST00000675694.1:c.388T=	ENSP00000501925.1:p.Ser130=
ENST00000676255.1:c.350T=	ENSP00000502459.1:n.350T=
ENST00000340850.9:c.388T=	ENSP00000344570.5:p.Ser130=
ENST00000377725.5:c.388T=	ENSP00000366954.1:p.Ser130=
ENST00000377728.7:c.388T=	ENSP00000366957.3:p.Ser130=
ENST00000377732.5:c.499T=	ENSP00000366961.1:p.Ser167=
ENST00000377740.4:c.619T=	ENSP00000366969.3:p.Ser207=
ENST00000377748.5:c.619T=	ENSP00000366977.1:p.Ser207=
ENST00000400913.5:c.388T=	ENSP00000383704.1:p.Ser130=
ENST00000400915.7:c.556T=	ENSP00000383706.3:p.Ser186=
ENST00000489097.5:n.864T=
ENST00000535355.5:c.595T=	ENSP00000441445.1:p.Ser199=
ENST00000537245.5:c.625T=	ENSP00000439625.1:p.Ser209=
NM_001042663.1:c.556T=	NP_001036128.1:p.Ser186=
NM_001042664.1:c.388T=	NP_001036129.1:p.Ser130=
NM_001042665.1:c.388T=	NP_001036130.1:p.Ser130=
NM_001265592.1:c.625T=	NP_001252521.1:p.Ser209=
NM_001265593.1:c.595T=	NP_001252522.1:p.Ser199=
NM_001265594.1:c.388T=	NP_001252523.1:p.Ser130=
NM_020631.4:c.388T=	NP_065682.2:p.Ser130=
NM_198681.3:c.619T=	NP_941374.2:p.Ser207=
NM_001042663.2:c.556T=	NP_001036128.1:p.Ser186=
NM_001265594.2:c.388T=	NP_001252523.1:p.Ser130=
NM_020631.5:c.388T=	NP_065682.2:p.Ser130=
NM_001042663.3:c.499T=	NP_001036128.2:p.Ser167=
NM_001265592.2:c.499T=	NP_001252521.2:p.Ser167=
NM_020631.6:c.388T= MANE Select	NP_065682.2:p.Ser130=
NM_198681.4:c.388T=	NP_941374.3:p.Ser130=