Canonical Allele Identifier: CA203666

Gene: PLEKHG5

Linked Data

• ClinVar Variation Id: 198896
• ClinVar RCV Id: RCV000180357 ; RCV000397744 ; RCV000536368 ; RCV001721129
• dbSNP Id: rs146651455
• ExAC: 1:6533415 C / T
• gnomAD v2: 1-6533415-C-T
• gnomAD v3: 1-6473355-C-T
• gnomAD v4: 1-6473355-C-T
• MyVariant Identifiers: chr1:g.6533415C>T (hg19) ; chr1:g.6473355C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6473355C>T , CM000663.2:g.6473355C>T	GRCh38
NC_000001.10:g.6533415C>T , CM000663.1:g.6533415C>T	GRCh37
NC_000001.9:g.6456002C>T	NCBI36
NG_007978.1:g.51655G>A , LRG_262:g.51655G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.691G>A	ENSP00000344570.5:p.Gly231Ser
ENST00000377728.8:c.691G>A MANE Select	ENSP00000366957.3:p.Gly231Ser
ENST00000377740.5:c.691G>A	ENSP00000366969.4:p.Gly231Ser
ENST00000377748.6:c.865G>A	ENSP00000366977.2:p.Gly289Ser
ENST00000400913.6:c.691G>A	ENSP00000383704.1:p.Gly231Ser
ENST00000400915.8:c.802G>A	ENSP00000383706.4:p.Gly268Ser
ENST00000489097.6:n.1167G>A
ENST00000535355.6:c.898G>A	ENSP00000441445.1:p.Gly300Ser
ENST00000537245.6:c.802G>A	ENSP00000439625.2:p.Gly268Ser
ENST00000673471.2:c.988G>A	ENSP00000500749.1:p.Gly330Ser
ENST00000674790.1:c.*903G>A	ENSP00000502815.1:n.*903G>A
ENST00000675123.1:c.691G>A	ENSP00000502132.1:p.Gly231Ser
ENST00000675548.1:c.*519G>A	ENSP00000502684.1:n.*519G>A
ENST00000675694.1:c.691G>A	ENSP00000501925.1:p.Gly231Ser
ENST00000340850.9:c.691G>A	ENSP00000344570.5:p.Gly231Ser
ENST00000377725.5:c.691G>A	ENSP00000366954.1:p.Gly231Ser
ENST00000377728.7:c.691G>A	ENSP00000366957.3:p.Gly231Ser
ENST00000377732.5:c.802G>A	ENSP00000366961.1:p.Gly268Ser
ENST00000377740.4:c.922G>A	ENSP00000366969.3:p.Gly308Ser
ENST00000377748.5:c.922G>A	ENSP00000366977.1:p.Gly308Ser
ENST00000400913.5:c.691G>A	ENSP00000383704.1:p.Gly231Ser
ENST00000400915.7:c.859G>A	ENSP00000383706.3:p.Gly287Ser
ENST00000489097.5:n.1167G>A
ENST00000535355.5:c.898G>A	ENSP00000441445.1:p.Gly300Ser
ENST00000537245.5:c.928G>A	ENSP00000439625.1:p.Gly310Ser
NM_001042663.1:c.859G>A	NP_001036128.1:p.Gly287Ser
NM_001042664.1:c.691G>A	NP_001036129.1:p.Gly231Ser
NM_001042665.1:c.691G>A	NP_001036130.1:p.Gly231Ser
NM_001265592.1:c.928G>A	NP_001252521.1:p.Gly310Ser
NM_001265593.1:c.898G>A	NP_001252522.1:p.Gly300Ser
NM_001265594.1:c.691G>A	NP_001252523.1:p.Gly231Ser
NM_020631.4:c.691G>A	NP_065682.2:p.Gly231Ser
NM_198681.3:c.922G>A	NP_941374.2:p.Gly308Ser
NM_001042663.2:c.859G>A	NP_001036128.1:p.Gly287Ser
NM_001265594.2:c.691G>A	NP_001252523.1:p.Gly231Ser
NM_020631.5:c.691G>A	NP_065682.2:p.Gly231Ser
NM_001042663.3:c.802G>A	NP_001036128.2:p.Gly268Ser
NM_001265592.2:c.802G>A	NP_001252521.2:p.Gly268Ser
NM_020631.6:c.691G>A MANE Select	NP_065682.2:p.Gly231Ser
NM_198681.4:c.691G>A	NP_941374.3:p.Gly231Ser