Canonical Allele Identifier: CA415833485

Gene: PLEKHG5

Linked Data

• ClinVar Variation Id: 2952176
• ClinVar RCV Id: RCV003815327
• MyVariant Identifiers: chr1:g.6533151G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6473091G>A , CM000663.2:g.6473091G>A	GRCh38
NC_000001.10:g.6533151G>A , CM000663.1:g.6533151G>A	GRCh37
NC_000001.9:g.6455738G>A	NCBI36
NG_007978.1:g.51919C>T , LRG_262:g.51919C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.879C>T	ENSP00000344570.5:p.Arg293=
ENST00000377728.8:c.879C>T MANE Select	ENSP00000366957.3:p.Arg293=
ENST00000377740.5:c.879C>T	ENSP00000366969.4:p.Arg293=
ENST00000377748.6:c.1053C>T	ENSP00000366977.2:p.Arg351=
ENST00000400913.6:c.879C>T	ENSP00000383704.1:p.Arg293=
ENST00000400915.8:c.990C>T	ENSP00000383706.4:p.Arg330=
ENST00000489097.6:n.1355C>T
ENST00000535355.6:c.1086C>T	ENSP00000441445.1:p.Arg362=
ENST00000537245.6:c.990C>T	ENSP00000439625.2:p.Arg330=
ENST00000673471.2:c.1176C>T	ENSP00000500749.1:p.Arg392=
ENST00000674790.1:c.*1091C>T	ENSP00000502815.1:n.*1091C>T
ENST00000675123.1:c.879C>T	ENSP00000502132.1:p.Arg293=
ENST00000675548.1:c.*707C>T	ENSP00000502684.1:n.*707C>T
ENST00000675694.1:c.879C>T	ENSP00000501925.1:p.Arg293=
ENST00000340850.9:c.879C>T	ENSP00000344570.5:p.Arg293=
ENST00000377725.5:c.879C>T	ENSP00000366954.1:p.Arg293=
ENST00000377728.7:c.879C>T	ENSP00000366957.3:p.Arg293=
ENST00000377732.5:c.990C>T	ENSP00000366961.1:p.Arg330=
ENST00000377740.4:c.1110C>T	ENSP00000366969.3:p.Arg370=
ENST00000377748.5:c.1110C>T	ENSP00000366977.1:p.Arg370=
ENST00000400913.5:c.879C>T	ENSP00000383704.1:p.Arg293=
ENST00000400915.7:c.1047C>T	ENSP00000383706.3:p.Arg349=
ENST00000489097.5:n.1355C>T
ENST00000535355.5:c.1086C>T	ENSP00000441445.1:p.Arg362=
ENST00000537245.5:c.1116C>T	ENSP00000439625.1:p.Arg372=
NM_001042663.1:c.1047C>T	NP_001036128.1:p.Arg349=
NM_001042664.1:c.879C>T	NP_001036129.1:p.Arg293=
NM_001042665.1:c.879C>T	NP_001036130.1:p.Arg293=
NM_001265592.1:c.1116C>T	NP_001252521.1:p.Arg372=
NM_001265593.1:c.1086C>T	NP_001252522.1:p.Arg362=
NM_001265594.1:c.879C>T	NP_001252523.1:p.Arg293=
NM_020631.4:c.879C>T	NP_065682.2:p.Arg293=
NM_198681.3:c.1110C>T	NP_941374.2:p.Arg370=
NM_001042663.2:c.1047C>T	NP_001036128.1:p.Arg349=
NM_001265594.2:c.879C>T	NP_001252523.1:p.Arg293=
NM_020631.5:c.879C>T	NP_065682.2:p.Arg293=
NM_001042663.3:c.990C>T	NP_001036128.2:p.Arg330=
NM_001265592.2:c.990C>T	NP_001252521.2:p.Arg330=
NM_020631.6:c.879C>T MANE Select	NP_065682.2:p.Arg293=
NM_198681.4:c.879C>T	NP_941374.3:p.Arg293=