Canonical Allele Identifier: CA415833907

Gene: PLEKHG5

Linked Data

• MyVariant Identifiers: chr1:g.6534100C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6474040C>T , CM000663.2:g.6474040C>T	GRCh38
NC_000001.10:g.6534100C>T , CM000663.1:g.6534100C>T	GRCh37
NC_000001.9:g.6456687C>T	NCBI36
NG_007978.1:g.50970G>A , LRG_262:g.50970G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.564G>A	ENSP00000344570.5:p.Gln188=
ENST00000377728.8:c.564G>A MANE Select	ENSP00000366957.3:p.Gln188=
ENST00000377740.5:c.564G>A	ENSP00000366969.4:p.Gln188=
ENST00000377748.6:c.738G>A	ENSP00000366977.2:p.Gln246=
ENST00000400913.6:c.564G>A	ENSP00000383704.1:p.Gln188=
ENST00000400915.8:c.675G>A	ENSP00000383706.4:p.Gln225=
ENST00000489097.6:n.1040G>A
ENST00000535355.6:c.771G>A	ENSP00000441445.1:p.Gln257=
ENST00000537245.6:c.675G>A	ENSP00000439625.2:p.Gln225=
ENST00000673471.2:c.861G>A	ENSP00000500749.1:p.Gln287=
ENST00000674790.1:c.*776G>A	ENSP00000502815.1:n.*776G>A
ENST00000675123.1:c.564G>A	ENSP00000502132.1:p.Gln188=
ENST00000675548.1:c.*392G>A	ENSP00000502684.1:n.*392G>A
ENST00000675694.1:c.564G>A	ENSP00000501925.1:p.Gln188=
ENST00000340850.9:c.564G>A	ENSP00000344570.5:p.Gln188=
ENST00000377725.5:c.564G>A	ENSP00000366954.1:p.Gln188=
ENST00000377728.7:c.564G>A	ENSP00000366957.3:p.Gln188=
ENST00000377732.5:c.675G>A	ENSP00000366961.1:p.Gln225=
ENST00000377740.4:c.795G>A	ENSP00000366969.3:p.Gln265=
ENST00000377748.5:c.795G>A	ENSP00000366977.1:p.Gln265=
ENST00000400913.5:c.564G>A	ENSP00000383704.1:p.Gln188=
ENST00000400915.7:c.732G>A	ENSP00000383706.3:p.Gln244=
ENST00000489097.5:n.1040G>A
ENST00000535355.5:c.771G>A	ENSP00000441445.1:p.Gln257=
ENST00000537245.5:c.801G>A	ENSP00000439625.1:p.Gln267=
NM_001042663.1:c.732G>A	NP_001036128.1:p.Gln244=
NM_001042664.1:c.564G>A	NP_001036129.1:p.Gln188=
NM_001042665.1:c.564G>A	NP_001036130.1:p.Gln188=
NM_001265592.1:c.801G>A	NP_001252521.1:p.Gln267=
NM_001265593.1:c.771G>A	NP_001252522.1:p.Gln257=
NM_001265594.1:c.564G>A	NP_001252523.1:p.Gln188=
NM_020631.4:c.564G>A	NP_065682.2:p.Gln188=
NM_198681.3:c.795G>A	NP_941374.2:p.Gln265=
NM_001042663.2:c.732G>A	NP_001036128.1:p.Gln244=
NM_001265594.2:c.564G>A	NP_001252523.1:p.Gln188=
NM_020631.5:c.564G>A	NP_065682.2:p.Gln188=
NM_001042663.3:c.675G>A	NP_001036128.2:p.Gln225=
NM_001265592.2:c.675G>A	NP_001252521.2:p.Gln225=
NM_020631.6:c.564G>A MANE Select	NP_065682.2:p.Gln188=
NM_198681.4:c.564G>A	NP_941374.3:p.Gln188=