Canonical Allele Identifier: CA416022353

Gene: PLEKHG5

Linked Data

• MyVariant Identifiers: chr1:g.6528172A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6468112A>T , CM000663.2:g.6468112A>T	GRCh38
NC_000001.10:g.6528172A>T , CM000663.1:g.6528172A>T	GRCh37
NC_000001.9:g.6450759A>T	NCBI36
NG_007978.1:g.56898T>A , LRG_262:g.56898T>A
NG_029910.1:g.3084T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.2724T>A	ENSP00000344570.5:p.Ala908=
ENST00000377728.8:c.2724T>A MANE Select	ENSP00000366957.3:p.Ala908=
ENST00000377740.5:c.2724T>A	ENSP00000366969.4:p.Ala908=
ENST00000377748.6:c.2898T>A	ENSP00000366977.2:p.Ala966=
ENST00000400913.6:c.2724T>A	ENSP00000383704.1:p.Ala908=
ENST00000400915.8:c.2835T>A	ENSP00000383706.4:p.Ala945=
ENST00000489097.6:n.3200T>A
ENST00000535355.6:c.2931T>A	ENSP00000441445.1:p.Ala977=
ENST00000537245.6:c.2835T>A	ENSP00000439625.2:p.Ala945=
ENST00000673471.2:c.3021T>A	ENSP00000500749.1:p.Ala1007=
ENST00000674790.1:c.*2936T>A	ENSP00000502815.1:n.*2936T>A
ENST00000675123.1:c.2250-219T>A	ENSP00000502132.1:n.2250-219T>A
ENST00000675548.1:c.*2552T>A	ENSP00000502684.1:n.*2552T>A
ENST00000675694.1:c.2724T>A	ENSP00000501925.1:p.Ala908=
ENST00000675976.1:c.597T>A	ENSP00000501611.1:p.Ala199=
ENST00000340850.9:c.2724T>A	ENSP00000344570.5:p.Ala908=
ENST00000377725.5:c.2724T>A	ENSP00000366954.1:p.Ala908=
ENST00000377728.7:c.2724T>A	ENSP00000366957.3:p.Ala908=
ENST00000377732.5:c.2835T>A	ENSP00000366961.1:p.Ala945=
ENST00000377740.4:c.2481-219T>A	ENSP00000366969.3:n.2481-219T>A
ENST00000377748.5:c.2955T>A	ENSP00000366977.1:p.Ala985=
ENST00000400913.5:c.2724T>A	ENSP00000383704.1:p.Ala908=
ENST00000400915.7:c.2892T>A	ENSP00000383706.3:p.Ala964=
ENST00000487949.4:n.1926T>A
ENST00000489097.5:n.3200T>A
ENST00000535355.5:c.2931T>A	ENSP00000441445.1:p.Ala977=
ENST00000537245.5:c.2961T>A	ENSP00000439625.1:p.Ala987=
NM_001042663.1:c.2892T>A	NP_001036128.1:p.Ala964=
NM_001042664.1:c.2724T>A	NP_001036129.1:p.Ala908=
NM_001042665.1:c.2724T>A	NP_001036130.1:p.Ala908=
NM_001265592.1:c.2961T>A	NP_001252521.1:p.Ala987=
NM_001265593.1:c.2931T>A	NP_001252522.1:p.Ala977=
NM_001265594.1:c.2724T>A	NP_001252523.1:p.Ala908=
NM_020631.4:c.2724T>A	NP_065682.2:p.Ala908=
NM_198681.3:c.2955T>A	NP_941374.2:p.Ala985=
NM_001042663.2:c.2892T>A	NP_001036128.1:p.Ala964=
NM_001265594.2:c.2724T>A	NP_001252523.1:p.Ala908=
NM_020631.5:c.2724T>A	NP_065682.2:p.Ala908=
NM_001042663.3:c.2835T>A	NP_001036128.2:p.Ala945=
NM_001265592.2:c.2835T>A	NP_001252521.2:p.Ala945=
NM_020631.6:c.2724T>A MANE Select	NP_065682.2:p.Ala908=
NM_198681.4:c.2724T>A	NP_941374.3:p.Ala908=