Canonical Allele Identifier: CA338124783

Gene: PLEKHG5

Linked Data

• MyVariant Identifiers: chr1:g.6530609T>G (hg19) ; chr1:g.6470549T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6470549T>G , CM000663.2:g.6470549T>G	GRCh38
NC_000001.10:g.6530609T>G , CM000663.1:g.6530609T>G	GRCh37
NC_000001.9:g.6453196T>G	NCBI36
NG_007978.1:g.54461A>C , LRG_262:g.54461A>C
NG_029910.1:g.647A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.1637A>C	ENSP00000344570.5:p.Asp546Ala
ENST00000377728.8:c.1637A>C MANE Select	ENSP00000366957.3:p.Asp546Ala
ENST00000377740.5:c.1637A>C	ENSP00000366969.4:p.Asp546Ala
ENST00000377748.6:c.1811A>C	ENSP00000366977.2:p.Asp604Ala
ENST00000400913.6:c.1637A>C	ENSP00000383704.1:p.Asp546Ala
ENST00000400915.8:c.1748A>C	ENSP00000383706.4:p.Asp583Ala
ENST00000489097.6:n.2113A>C
ENST00000535355.6:c.1844A>C	ENSP00000441445.1:p.Asp615Ala
ENST00000537245.6:c.1748A>C	ENSP00000439625.2:p.Asp583Ala
ENST00000673471.2:c.1934A>C	ENSP00000500749.1:p.Asp645Ala
ENST00000674790.1:c.*1849A>C	ENSP00000502815.1:n.*1849A>C
ENST00000674943.1:n.299A>C
ENST00000675123.1:c.1637A>C	ENSP00000502132.1:p.Asp546Ala
ENST00000675548.1:c.*1465A>C	ENSP00000502684.1:n.*1465A>C
ENST00000675694.1:c.1637A>C	ENSP00000501925.1:p.Asp546Ala
ENST00000676401.1:n.184A>C
ENST00000340850.9:c.1637A>C	ENSP00000344570.5:p.Asp546Ala
ENST00000377725.5:c.1637A>C	ENSP00000366954.1:p.Asp546Ala
ENST00000377728.7:c.1637A>C	ENSP00000366957.3:p.Asp546Ala
ENST00000377732.5:c.1748A>C	ENSP00000366961.1:p.Asp583Ala
ENST00000377740.4:c.1868A>C	ENSP00000366969.3:p.Asp623Ala
ENST00000377748.5:c.1868A>C	ENSP00000366977.1:p.Asp623Ala
ENST00000400913.5:c.1637A>C	ENSP00000383704.1:p.Asp546Ala
ENST00000400915.7:c.1805A>C	ENSP00000383706.3:p.Asp602Ala
ENST00000487949.4:n.839A>C
ENST00000489097.5:n.2113A>C
ENST00000535355.5:c.1844A>C	ENSP00000441445.1:p.Asp615Ala
ENST00000537245.5:c.1874A>C	ENSP00000439625.1:p.Asp625Ala
NM_001042663.1:c.1805A>C	NP_001036128.1:p.Asp602Ala
NM_001042664.1:c.1637A>C	NP_001036129.1:p.Asp546Ala
NM_001042665.1:c.1637A>C	NP_001036130.1:p.Asp546Ala
NM_001265592.1:c.1874A>C	NP_001252521.1:p.Asp625Ala
NM_001265593.1:c.1844A>C	NP_001252522.1:p.Asp615Ala
NM_001265594.1:c.1637A>C	NP_001252523.1:p.Asp546Ala
NM_020631.4:c.1637A>C	NP_065682.2:p.Asp546Ala
NM_198681.3:c.1868A>C	NP_941374.2:p.Asp623Ala
NM_001042663.2:c.1805A>C	NP_001036128.1:p.Asp602Ala
NM_001265594.2:c.1637A>C	NP_001252523.1:p.Asp546Ala
NM_020631.5:c.1637A>C	NP_065682.2:p.Asp546Ala
NM_001042663.3:c.1748A>C	NP_001036128.2:p.Asp583Ala
NM_001265592.2:c.1748A>C	NP_001252521.2:p.Asp583Ala
NM_020631.6:c.1637A>C MANE Select	NP_065682.2:p.Asp546Ala
NM_198681.4:c.1637A>C	NP_941374.3:p.Asp546Ala