Canonical Allele Identifier: CA338125142

Gene: PLEKHG5

Linked Data

• MyVariant Identifiers: chr1:g.6530628C>A (hg19) ; chr1:g.6470568C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6470568C>A , CM000663.2:g.6470568C>A	GRCh38
NC_000001.10:g.6530628C>A , CM000663.1:g.6530628C>A	GRCh37
NC_000001.9:g.6453215C>A	NCBI36
NG_007978.1:g.54442G>T , LRG_262:g.54442G>T
NG_029910.1:g.628G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.1618G>T	ENSP00000344570.5:p.Ala540Ser
ENST00000377728.8:c.1618G>T MANE Select	ENSP00000366957.3:p.Ala540Ser
ENST00000377740.5:c.1618G>T	ENSP00000366969.4:p.Ala540Ser
ENST00000377748.6:c.1792G>T	ENSP00000366977.2:p.Ala598Ser
ENST00000400913.6:c.1618G>T	ENSP00000383704.1:p.Ala540Ser
ENST00000400915.8:c.1729G>T	ENSP00000383706.4:p.Ala577Ser
ENST00000489097.6:n.2094G>T
ENST00000535355.6:c.1825G>T	ENSP00000441445.1:p.Ala609Ser
ENST00000537245.6:c.1729G>T	ENSP00000439625.2:p.Ala577Ser
ENST00000673471.2:c.1915G>T	ENSP00000500749.1:p.Ala639Ser
ENST00000674790.1:c.*1830G>T	ENSP00000502815.1:n.*1830G>T
ENST00000674943.1:n.280G>T
ENST00000675123.1:c.1618G>T	ENSP00000502132.1:p.Ala540Ser
ENST00000675548.1:c.*1446G>T	ENSP00000502684.1:n.*1446G>T
ENST00000675694.1:c.1618G>T	ENSP00000501925.1:p.Ala540Ser
ENST00000676401.1:n.165G>T
ENST00000340850.9:c.1618G>T	ENSP00000344570.5:p.Ala540Ser
ENST00000377725.5:c.1618G>T	ENSP00000366954.1:p.Ala540Ser
ENST00000377728.7:c.1618G>T	ENSP00000366957.3:p.Ala540Ser
ENST00000377732.5:c.1729G>T	ENSP00000366961.1:p.Ala577Ser
ENST00000377740.4:c.1849G>T	ENSP00000366969.3:p.Ala617Ser
ENST00000377748.5:c.1849G>T	ENSP00000366977.1:p.Ala617Ser
ENST00000400913.5:c.1618G>T	ENSP00000383704.1:p.Ala540Ser
ENST00000400915.7:c.1786G>T	ENSP00000383706.3:p.Ala596Ser
ENST00000487949.4:n.820G>T
ENST00000489097.5:n.2094G>T
ENST00000535355.5:c.1825G>T	ENSP00000441445.1:p.Ala609Ser
ENST00000537245.5:c.1855G>T	ENSP00000439625.1:p.Ala619Ser
NM_001042663.1:c.1786G>T	NP_001036128.1:p.Ala596Ser
NM_001042664.1:c.1618G>T	NP_001036129.1:p.Ala540Ser
NM_001042665.1:c.1618G>T	NP_001036130.1:p.Ala540Ser
NM_001265592.1:c.1855G>T	NP_001252521.1:p.Ala619Ser
NM_001265593.1:c.1825G>T	NP_001252522.1:p.Ala609Ser
NM_001265594.1:c.1618G>T	NP_001252523.1:p.Ala540Ser
NM_020631.4:c.1618G>T	NP_065682.2:p.Ala540Ser
NM_198681.3:c.1849G>T	NP_941374.2:p.Ala617Ser
NM_001042663.2:c.1786G>T	NP_001036128.1:p.Ala596Ser
NM_001265594.2:c.1618G>T	NP_001252523.1:p.Ala540Ser
NM_020631.5:c.1618G>T	NP_065682.2:p.Ala540Ser
NM_001042663.3:c.1729G>T	NP_001036128.2:p.Ala577Ser
NM_001265592.2:c.1729G>T	NP_001252521.2:p.Ala577Ser
NM_020631.6:c.1618G>T MANE Select	NP_065682.2:p.Ala540Ser
NM_198681.4:c.1618G>T	NP_941374.3:p.Ala540Ser