Canonical Allele Identifier: CA561811

Gene: PLEKHG5

Linked Data

• ClinVar Variation Id: 1089409
• ClinVar RCV Id: RCV001408221
• dbSNP Id: rs767157981
• ExAC: 1:6534106 G / A
• gnomAD v2: 1-6534106-G-A
• gnomAD v3: 1-6474046-G-A
• gnomAD v4: 1-6474046-G-A
• MyVariant Identifiers: chr1:g.6534106G>A (hg19) ; chr1:g.6474046G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6474046G>A , CM000663.2:g.6474046G>A	GRCh38
NC_000001.10:g.6534106G>A , CM000663.1:g.6534106G>A	GRCh37
NC_000001.9:g.6456693G>A	NCBI36
NG_007978.1:g.50964C>T , LRG_262:g.50964C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.558C>T	ENSP00000344570.5:p.Asp186=
ENST00000377728.8:c.558C>T MANE Select	ENSP00000366957.3:p.Asp186=
ENST00000377740.5:c.558C>T	ENSP00000366969.4:p.Asp186=
ENST00000377748.6:c.732C>T	ENSP00000366977.2:p.Asp244=
ENST00000400913.6:c.558C>T	ENSP00000383704.1:p.Asp186=
ENST00000400915.8:c.669C>T	ENSP00000383706.4:p.Asp223=
ENST00000489097.6:n.1034C>T
ENST00000535355.6:c.765C>T	ENSP00000441445.1:p.Asp255=
ENST00000537245.6:c.669C>T	ENSP00000439625.2:p.Asp223=
ENST00000673471.2:c.855C>T	ENSP00000500749.1:p.Asp285=
ENST00000674790.1:c.*770C>T	ENSP00000502815.1:n.*770C>T
ENST00000675123.1:c.558C>T	ENSP00000502132.1:p.Asp186=
ENST00000675548.1:c.*386C>T	ENSP00000502684.1:n.*386C>T
ENST00000675694.1:c.558C>T	ENSP00000501925.1:p.Asp186=
ENST00000340850.9:c.558C>T	ENSP00000344570.5:p.Asp186=
ENST00000377725.5:c.558C>T	ENSP00000366954.1:p.Asp186=
ENST00000377728.7:c.558C>T	ENSP00000366957.3:p.Asp186=
ENST00000377732.5:c.669C>T	ENSP00000366961.1:p.Asp223=
ENST00000377740.4:c.789C>T	ENSP00000366969.3:p.Asp263=
ENST00000377748.5:c.789C>T	ENSP00000366977.1:p.Asp263=
ENST00000400913.5:c.558C>T	ENSP00000383704.1:p.Asp186=
ENST00000400915.7:c.726C>T	ENSP00000383706.3:p.Asp242=
ENST00000489097.5:n.1034C>T
ENST00000535355.5:c.765C>T	ENSP00000441445.1:p.Asp255=
ENST00000537245.5:c.795C>T	ENSP00000439625.1:p.Asp265=
NM_001042663.1:c.726C>T	NP_001036128.1:p.Asp242=
NM_001042664.1:c.558C>T	NP_001036129.1:p.Asp186=
NM_001042665.1:c.558C>T	NP_001036130.1:p.Asp186=
NM_001265592.1:c.795C>T	NP_001252521.1:p.Asp265=
NM_001265593.1:c.765C>T	NP_001252522.1:p.Asp255=
NM_001265594.1:c.558C>T	NP_001252523.1:p.Asp186=
NM_020631.4:c.558C>T	NP_065682.2:p.Asp186=
NM_198681.3:c.789C>T	NP_941374.2:p.Asp263=
NM_001042663.2:c.726C>T	NP_001036128.1:p.Asp242=
NM_001265594.2:c.558C>T	NP_001252523.1:p.Asp186=
NM_020631.5:c.558C>T	NP_065682.2:p.Asp186=
NM_001042663.3:c.669C>T	NP_001036128.2:p.Asp223=
NM_001265592.2:c.669C>T	NP_001252521.2:p.Asp223=
NM_020631.6:c.558C>T MANE Select	NP_065682.2:p.Asp186=
NM_198681.4:c.558C>T	NP_941374.3:p.Asp186=