Canonical Allele Identifier: CA416022685

Gene: PLEKHG5

Linked Data

• MyVariant Identifiers: chr1:g.6528256G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6468196G>T , CM000663.2:g.6468196G>T	GRCh38
NC_000001.10:g.6528256G>T , CM000663.1:g.6528256G>T	GRCh37
NC_000001.9:g.6450843G>T	NCBI36
NG_007978.1:g.56814C>A , LRG_262:g.56814C>A
NG_029910.1:g.3000C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.2640C>A	ENSP00000344570.5:p.Ala880=
ENST00000377728.8:c.2640C>A MANE Select	ENSP00000366957.3:p.Ala880=
ENST00000377740.5:c.2640C>A	ENSP00000366969.4:p.Ala880=
ENST00000377748.6:c.2814C>A	ENSP00000366977.2:p.Ala938=
ENST00000400913.6:c.2640C>A	ENSP00000383704.1:p.Ala880=
ENST00000400915.8:c.2751C>A	ENSP00000383706.4:p.Ala917=
ENST00000489097.6:n.3116C>A
ENST00000535355.6:c.2847C>A	ENSP00000441445.1:p.Ala949=
ENST00000537245.6:c.2751C>A	ENSP00000439625.2:p.Ala917=
ENST00000673471.2:c.2937C>A	ENSP00000500749.1:p.Ala979=
ENST00000674790.1:c.*2852C>A	ENSP00000502815.1:n.*2852C>A
ENST00000675123.1:c.2250-303C>A	ENSP00000502132.1:n.2250-303C>A
ENST00000675548.1:c.*2468C>A	ENSP00000502684.1:n.*2468C>A
ENST00000675694.1:c.2640C>A	ENSP00000501925.1:p.Ala880=
ENST00000675976.1:c.513C>A	ENSP00000501611.1:p.Ala171=
ENST00000340850.9:c.2640C>A	ENSP00000344570.5:p.Ala880=
ENST00000377725.5:c.2640C>A	ENSP00000366954.1:p.Ala880=
ENST00000377728.7:c.2640C>A	ENSP00000366957.3:p.Ala880=
ENST00000377732.5:c.2751C>A	ENSP00000366961.1:p.Ala917=
ENST00000377740.4:c.2481-303C>A	ENSP00000366969.3:n.2481-303C>A
ENST00000377748.5:c.2871C>A	ENSP00000366977.1:p.Ala957=
ENST00000400913.5:c.2640C>A	ENSP00000383704.1:p.Ala880=
ENST00000400915.7:c.2808C>A	ENSP00000383706.3:p.Ala936=
ENST00000487949.4:n.1842C>A
ENST00000489097.5:n.3116C>A
ENST00000535355.5:c.2847C>A	ENSP00000441445.1:p.Ala949=
ENST00000537245.5:c.2877C>A	ENSP00000439625.1:p.Ala959=
NM_001042663.1:c.2808C>A	NP_001036128.1:p.Ala936=
NM_001042664.1:c.2640C>A	NP_001036129.1:p.Ala880=
NM_001042665.1:c.2640C>A	NP_001036130.1:p.Ala880=
NM_001265592.1:c.2877C>A	NP_001252521.1:p.Ala959=
NM_001265593.1:c.2847C>A	NP_001252522.1:p.Ala949=
NM_001265594.1:c.2640C>A	NP_001252523.1:p.Ala880=
NM_020631.4:c.2640C>A	NP_065682.2:p.Ala880=
NM_198681.3:c.2871C>A	NP_941374.2:p.Ala957=
NM_001042663.2:c.2808C>A	NP_001036128.1:p.Ala936=
NM_001265594.2:c.2640C>A	NP_001252523.1:p.Ala880=
NM_020631.5:c.2640C>A	NP_065682.2:p.Ala880=
NM_001042663.3:c.2751C>A	NP_001036128.2:p.Ala917=
NM_001265592.2:c.2751C>A	NP_001252521.2:p.Ala917=
NM_020631.6:c.2640C>A MANE Select	NP_065682.2:p.Ala880=
NM_198681.4:c.2640C>A	NP_941374.3:p.Ala880=