Canonical Allele Identifier: CA338124793
Gene: PLEKHG5 HGNC NCBI

Linked Data

dbSNP Id: rs1176837922

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.6470550C>T , CM000663.2:g.6470550C>T GRCh38
NC_000001.10:g.6530610C>T , CM000663.1:g.6530610C>T GRCh37
NC_000001.9:g.6453197C>T NCBI36
NG_007978.1:g.54460G>A , LRG_262:g.54460G>A
NG_029910.1:g.646G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000340850.10:c.1636G>A ENSP00000344570.5:p.Asp546Asn
ENST00000377728.8:c.1636G>A MANE Select ENSP00000366957.3:p.Asp546Asn
ENST00000377740.5:c.1636G>A ENSP00000366969.4:p.Asp546Asn
ENST00000377748.6:c.1810G>A ENSP00000366977.2:p.Asp604Asn
ENST00000400913.6:c.1636G>A ENSP00000383704.1:p.Asp546Asn
ENST00000400915.8:c.1747G>A ENSP00000383706.4:p.Asp583Asn
ENST00000489097.6:n.2112G>A
ENST00000535355.6:c.1843G>A ENSP00000441445.1:p.Asp615Asn
ENST00000537245.6:c.1747G>A ENSP00000439625.2:p.Asp583Asn
ENST00000673471.2:c.1933G>A ENSP00000500749.1:p.Asp645Asn
ENST00000674790.1:c.*1848G>A ENSP00000502815.1:n.*1848G>A
ENST00000674943.1:n.298G>A
ENST00000675123.1:c.1636G>A ENSP00000502132.1:p.Asp546Asn
ENST00000675548.1:c.*1464G>A ENSP00000502684.1:n.*1464G>A
ENST00000675694.1:c.1636G>A ENSP00000501925.1:p.Asp546Asn
ENST00000676401.1:n.183G>A
ENST00000340850.9:c.1636G>A ENSP00000344570.5:p.Asp546Asn
ENST00000377725.5:c.1636G>A ENSP00000366954.1:p.Asp546Asn
ENST00000377728.7:c.1636G>A ENSP00000366957.3:p.Asp546Asn
ENST00000377732.5:c.1747G>A ENSP00000366961.1:p.Asp583Asn
ENST00000377740.4:c.1867G>A ENSP00000366969.3:p.Asp623Asn
ENST00000377748.5:c.1867G>A ENSP00000366977.1:p.Asp623Asn
ENST00000400913.5:c.1636G>A ENSP00000383704.1:p.Asp546Asn
ENST00000400915.7:c.1804G>A ENSP00000383706.3:p.Asp602Asn
ENST00000487949.4:n.838G>A
ENST00000489097.5:n.2112G>A
ENST00000535355.5:c.1843G>A ENSP00000441445.1:p.Asp615Asn
ENST00000537245.5:c.1873G>A ENSP00000439625.1:p.Asp625Asn
NM_001042663.1:c.1804G>A NP_001036128.1:p.Asp602Asn
NM_001042664.1:c.1636G>A NP_001036129.1:p.Asp546Asn
NM_001042665.1:c.1636G>A NP_001036130.1:p.Asp546Asn
NM_001265592.1:c.1873G>A NP_001252521.1:p.Asp625Asn
NM_001265593.1:c.1843G>A NP_001252522.1:p.Asp615Asn
NM_001265594.1:c.1636G>A NP_001252523.1:p.Asp546Asn
NM_020631.4:c.1636G>A NP_065682.2:p.Asp546Asn
NM_198681.3:c.1867G>A NP_941374.2:p.Asp623Asn
NM_001042663.2:c.1804G>A NP_001036128.1:p.Asp602Asn
NM_001265594.2:c.1636G>A NP_001252523.1:p.Asp546Asn
NM_020631.5:c.1636G>A NP_065682.2:p.Asp546Asn
NM_001042663.3:c.1747G>A NP_001036128.2:p.Asp583Asn
NM_001265592.2:c.1747G>A NP_001252521.2:p.Asp583Asn
NM_020631.6:c.1636G>A MANE Select NP_065682.2:p.Asp546Asn
NM_198681.4:c.1636G>A NP_941374.3:p.Asp546Asn