Canonical Allele Identifier: CA338139405

Gene: PLEKHG5

Linked Data

• MyVariant Identifiers: chr1:g.6534591A>T (hg19) ; chr1:g.6474531A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6474531A>T , CM000663.2:g.6474531A>T	GRCh38
NC_000001.10:g.6534591A>T , CM000663.1:g.6534591A>T	GRCh37
NC_000001.9:g.6457178A>T	NCBI36
NG_007978.1:g.50479T>A , LRG_262:g.50479T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.359T>A	ENSP00000344570.5:p.Ile120Asn
ENST00000377728.8:c.359T>A MANE Select	ENSP00000366957.3:p.Ile120Asn
ENST00000377740.5:c.359T>A	ENSP00000366969.4:p.Ile120Asn
ENST00000377748.6:c.533T>A	ENSP00000366977.2:p.Ile178Asn
ENST00000400913.6:c.359T>A	ENSP00000383704.1:p.Ile120Asn
ENST00000400915.8:c.470T>A	ENSP00000383706.4:p.Ile157Asn
ENST00000489097.6:n.835T>A
ENST00000535355.6:c.566T>A	ENSP00000441445.1:p.Ile189Asn
ENST00000537245.6:c.470T>A	ENSP00000439625.2:p.Ile157Asn
ENST00000673471.2:c.656T>A	ENSP00000500749.1:p.Ile219Asn
ENST00000674790.1:c.*571T>A	ENSP00000502815.1:n.*571T>A
ENST00000675123.1:c.359T>A	ENSP00000502132.1:p.Ile120Asn
ENST00000675548.1:c.*187T>A	ENSP00000502684.1:n.*187T>A
ENST00000675694.1:c.359T>A	ENSP00000501925.1:p.Ile120Asn
ENST00000676255.1:c.321T>A	ENSP00000502459.1:n.321T>A
ENST00000340850.9:c.359T>A	ENSP00000344570.5:p.Ile120Asn
ENST00000377725.5:c.359T>A	ENSP00000366954.1:p.Ile120Asn
ENST00000377728.7:c.359T>A	ENSP00000366957.3:p.Ile120Asn
ENST00000377732.5:c.470T>A	ENSP00000366961.1:p.Ile157Asn
ENST00000377740.4:c.590T>A	ENSP00000366969.3:p.Ile197Asn
ENST00000377748.5:c.590T>A	ENSP00000366977.1:p.Ile197Asn
ENST00000400913.5:c.359T>A	ENSP00000383704.1:p.Ile120Asn
ENST00000400915.7:c.527T>A	ENSP00000383706.3:p.Ile176Asn
ENST00000489097.5:n.835T>A
ENST00000535355.5:c.566T>A	ENSP00000441445.1:p.Ile189Asn
ENST00000537245.5:c.596T>A	ENSP00000439625.1:p.Ile199Asn
NM_001042663.1:c.527T>A	NP_001036128.1:p.Ile176Asn
NM_001042664.1:c.359T>A	NP_001036129.1:p.Ile120Asn
NM_001042665.1:c.359T>A	NP_001036130.1:p.Ile120Asn
NM_001265592.1:c.596T>A	NP_001252521.1:p.Ile199Asn
NM_001265593.1:c.566T>A	NP_001252522.1:p.Ile189Asn
NM_001265594.1:c.359T>A	NP_001252523.1:p.Ile120Asn
NM_020631.4:c.359T>A	NP_065682.2:p.Ile120Asn
NM_198681.3:c.590T>A	NP_941374.2:p.Ile197Asn
NM_001042663.2:c.527T>A	NP_001036128.1:p.Ile176Asn
NM_001265594.2:c.359T>A	NP_001252523.1:p.Ile120Asn
NM_020631.5:c.359T>A	NP_065682.2:p.Ile120Asn
NM_001042663.3:c.470T>A	NP_001036128.2:p.Ile157Asn
NM_001265592.2:c.470T>A	NP_001252521.2:p.Ile157Asn
NM_020631.6:c.359T>A MANE Select	NP_065682.2:p.Ile120Asn
NM_198681.4:c.359T>A	NP_941374.3:p.Ile120Asn