Canonical Allele Identifier: CA415833971
Gene: PLEKHG5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.6534172G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.6474112G>A , CM000663.2:g.6474112G>A GRCh38
NC_000001.10:g.6534172G>A , CM000663.1:g.6534172G>A GRCh37
NC_000001.9:g.6456759G>A NCBI36
NG_007978.1:g.50898C>T , LRG_262:g.50898C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000340850.10:c.492C>T ENSP00000344570.5:p.Ser164=
ENST00000377728.8:c.492C>T MANE Select ENSP00000366957.3:p.Ser164=
ENST00000377740.5:c.492C>T ENSP00000366969.4:p.Ser164=
ENST00000377748.6:c.666C>T ENSP00000366977.2:p.Ser222=
ENST00000400913.6:c.492C>T ENSP00000383704.1:p.Ser164=
ENST00000400915.8:c.603C>T ENSP00000383706.4:p.Ser201=
ENST00000489097.6:n.968C>T
ENST00000535355.6:c.699C>T ENSP00000441445.1:p.Ser233=
ENST00000537245.6:c.603C>T ENSP00000439625.2:p.Ser201=
ENST00000673471.2:c.789C>T ENSP00000500749.1:p.Ser263=
ENST00000674790.1:c.*704C>T ENSP00000502815.1:n.*704C>T
ENST00000675123.1:c.492C>T ENSP00000502132.1:p.Ser164=
ENST00000675548.1:c.*320C>T ENSP00000502684.1:n.*320C>T
ENST00000675694.1:c.492C>T ENSP00000501925.1:p.Ser164=
ENST00000340850.9:c.492C>T ENSP00000344570.5:p.Ser164=
ENST00000377725.5:c.492C>T ENSP00000366954.1:p.Ser164=
ENST00000377728.7:c.492C>T ENSP00000366957.3:p.Ser164=
ENST00000377732.5:c.603C>T ENSP00000366961.1:p.Ser201=
ENST00000377740.4:c.723C>T ENSP00000366969.3:p.Ser241=
ENST00000377748.5:c.723C>T ENSP00000366977.1:p.Ser241=
ENST00000400913.5:c.492C>T ENSP00000383704.1:p.Ser164=
ENST00000400915.7:c.660C>T ENSP00000383706.3:p.Ser220=
ENST00000489097.5:n.968C>T
ENST00000535355.5:c.699C>T ENSP00000441445.1:p.Ser233=
ENST00000537245.5:c.729C>T ENSP00000439625.1:p.Ser243=
NM_001042663.1:c.660C>T NP_001036128.1:p.Ser220=
NM_001042664.1:c.492C>T NP_001036129.1:p.Ser164=
NM_001042665.1:c.492C>T NP_001036130.1:p.Ser164=
NM_001265592.1:c.729C>T NP_001252521.1:p.Ser243=
NM_001265593.1:c.699C>T NP_001252522.1:p.Ser233=
NM_001265594.1:c.492C>T NP_001252523.1:p.Ser164=
NM_020631.4:c.492C>T NP_065682.2:p.Ser164=
NM_198681.3:c.723C>T NP_941374.2:p.Ser241=
NM_001042663.2:c.660C>T NP_001036128.1:p.Ser220=
NM_001265594.2:c.492C>T NP_001252523.1:p.Ser164=
NM_020631.5:c.492C>T NP_065682.2:p.Ser164=
NM_001042663.3:c.603C>T NP_001036128.2:p.Ser201=
NM_001265592.2:c.603C>T NP_001252521.2:p.Ser201=
NM_020631.6:c.492C>T MANE Select NP_065682.2:p.Ser164=
NM_198681.4:c.492C>T NP_941374.3:p.Ser164=