Canonical Allele Identifier: CA338133553

Gene: PLEKHG5

Linked Data

• dbSNP Id: rs773966438
• gnomAD v3: 1-6473008-C-G
• gnomAD v4: 1-6473008-C-G
• MyVariant Identifiers: chr1:g.6533068C>G (hg19) ; chr1:g.6473008C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6473008C>G , CM000663.2:g.6473008C>G	GRCh38
NC_000001.10:g.6533068C>G , CM000663.1:g.6533068C>G	GRCh37
NC_000001.9:g.6455655C>G	NCBI36
NG_007978.1:g.52002G>C , LRG_262:g.52002G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000340850.10:c.962G>C	ENSP00000344570.5:p.Arg321Pro
ENST00000377728.8:c.962G>C MANE Select	ENSP00000366957.3:p.Arg321Pro
ENST00000377740.5:c.962G>C	ENSP00000366969.4:p.Arg321Pro
ENST00000377748.6:c.1136G>C	ENSP00000366977.2:p.Arg379Pro
ENST00000400913.6:c.962G>C	ENSP00000383704.1:p.Arg321Pro
ENST00000400915.8:c.1073G>C	ENSP00000383706.4:p.Arg358Pro
ENST00000489097.6:n.1438G>C
ENST00000535355.6:c.1169G>C	ENSP00000441445.1:p.Arg390Pro
ENST00000537245.6:c.1073G>C	ENSP00000439625.2:p.Arg358Pro
ENST00000673471.2:c.1259G>C	ENSP00000500749.1:p.Arg420Pro
ENST00000674790.1:c.*1174G>C	ENSP00000502815.1:n.*1174G>C
ENST00000675123.1:c.962G>C	ENSP00000502132.1:p.Arg321Pro
ENST00000675548.1:c.*790G>C	ENSP00000502684.1:n.*790G>C
ENST00000675694.1:c.962G>C	ENSP00000501925.1:p.Arg321Pro
ENST00000340850.9:c.962G>C	ENSP00000344570.5:p.Arg321Pro
ENST00000377725.5:c.962G>C	ENSP00000366954.1:p.Arg321Pro
ENST00000377728.7:c.962G>C	ENSP00000366957.3:p.Arg321Pro
ENST00000377732.5:c.1073G>C	ENSP00000366961.1:p.Arg358Pro
ENST00000377740.4:c.1193G>C	ENSP00000366969.3:p.Arg398Pro
ENST00000377748.5:c.1193G>C	ENSP00000366977.1:p.Arg398Pro
ENST00000400913.5:c.962G>C	ENSP00000383704.1:p.Arg321Pro
ENST00000400915.7:c.1130G>C	ENSP00000383706.3:p.Arg377Pro
ENST00000489097.5:n.1438G>C
ENST00000535355.5:c.1169G>C	ENSP00000441445.1:p.Arg390Pro
ENST00000537245.5:c.1199G>C	ENSP00000439625.1:p.Arg400Pro
NM_001042663.1:c.1130G>C	NP_001036128.1:p.Arg377Pro
NM_001042664.1:c.962G>C	NP_001036129.1:p.Arg321Pro
NM_001042665.1:c.962G>C	NP_001036130.1:p.Arg321Pro
NM_001265592.1:c.1199G>C	NP_001252521.1:p.Arg400Pro
NM_001265593.1:c.1169G>C	NP_001252522.1:p.Arg390Pro
NM_001265594.1:c.962G>C	NP_001252523.1:p.Arg321Pro
NM_020631.4:c.962G>C	NP_065682.2:p.Arg321Pro
NM_198681.3:c.1193G>C	NP_941374.2:p.Arg398Pro
NM_001042663.2:c.1130G>C	NP_001036128.1:p.Arg377Pro
NM_001265594.2:c.962G>C	NP_001252523.1:p.Arg321Pro
NM_020631.5:c.962G>C	NP_065682.2:p.Arg321Pro
NM_001042663.3:c.1073G>C	NP_001036128.2:p.Arg358Pro
NM_001265592.2:c.1073G>C	NP_001252521.2:p.Arg358Pro
NM_020631.6:c.962G>C MANE Select	NP_065682.2:p.Arg321Pro
NM_198681.4:c.962G>C	NP_941374.3:p.Arg321Pro