Canonical Allele Identifier: CA338125756
Gene: PLEKHG5 HGNC NCBI

Linked Data

dbSNP Id: rs1010507470

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.6470608G>C , CM000663.2:g.6470608G>C GRCh38
NC_000001.10:g.6530668G>C , CM000663.1:g.6530668G>C GRCh37
NC_000001.9:g.6453255G>C NCBI36
NG_007978.1:g.54402C>G , LRG_262:g.54402C>G
NG_029910.1:g.588C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000340850.10:c.1578C>G ENSP00000344570.5:p.Asn526Lys
ENST00000377728.8:c.1578C>G MANE Select ENSP00000366957.3:p.Asn526Lys
ENST00000377740.5:c.1578C>G ENSP00000366969.4:p.Asn526Lys
ENST00000377748.6:c.1752C>G ENSP00000366977.2:p.Asn584Lys
ENST00000400913.6:c.1578C>G ENSP00000383704.1:p.Asn526Lys
ENST00000400915.8:c.1689C>G ENSP00000383706.4:p.Asn563Lys
ENST00000489097.6:n.2054C>G
ENST00000535355.6:c.1785C>G ENSP00000441445.1:p.Asn595Lys
ENST00000537245.6:c.1689C>G ENSP00000439625.2:p.Asn563Lys
ENST00000673471.2:c.1875C>G ENSP00000500749.1:p.Asn625Lys
ENST00000674790.1:c.*1790C>G ENSP00000502815.1:n.*1790C>G
ENST00000674943.1:n.240C>G
ENST00000675123.1:c.1578C>G ENSP00000502132.1:p.Asn526Lys
ENST00000675548.1:c.*1406C>G ENSP00000502684.1:n.*1406C>G
ENST00000675694.1:c.1578C>G ENSP00000501925.1:p.Asn526Lys
ENST00000676401.1:n.125C>G
ENST00000340850.9:c.1578C>G ENSP00000344570.5:p.Asn526Lys
ENST00000377725.5:c.1578C>G ENSP00000366954.1:p.Asn526Lys
ENST00000377728.7:c.1578C>G ENSP00000366957.3:p.Asn526Lys
ENST00000377732.5:c.1689C>G ENSP00000366961.1:p.Asn563Lys
ENST00000377740.4:c.1809C>G ENSP00000366969.3:p.Asn603Lys
ENST00000377748.5:c.1809C>G ENSP00000366977.1:p.Asn603Lys
ENST00000400913.5:c.1578C>G ENSP00000383704.1:p.Asn526Lys
ENST00000400915.7:c.1746C>G ENSP00000383706.3:p.Asn582Lys
ENST00000487949.4:n.780C>G
ENST00000489097.5:n.2054C>G
ENST00000535355.5:c.1785C>G ENSP00000441445.1:p.Asn595Lys
ENST00000537245.5:c.1815C>G ENSP00000439625.1:p.Asn605Lys
NM_001042663.1:c.1746C>G NP_001036128.1:p.Asn582Lys
NM_001042664.1:c.1578C>G NP_001036129.1:p.Asn526Lys
NM_001042665.1:c.1578C>G NP_001036130.1:p.Asn526Lys
NM_001265592.1:c.1815C>G NP_001252521.1:p.Asn605Lys
NM_001265593.1:c.1785C>G NP_001252522.1:p.Asn595Lys
NM_001265594.1:c.1578C>G NP_001252523.1:p.Asn526Lys
NM_020631.4:c.1578C>G NP_065682.2:p.Asn526Lys
NM_198681.3:c.1809C>G NP_941374.2:p.Asn603Lys
NM_001042663.2:c.1746C>G NP_001036128.1:p.Asn582Lys
NM_001265594.2:c.1578C>G NP_001252523.1:p.Asn526Lys
NM_020631.5:c.1578C>G NP_065682.2:p.Asn526Lys
NM_001042663.3:c.1689C>G NP_001036128.2:p.Asn563Lys
NM_001265592.2:c.1689C>G NP_001252521.2:p.Asn563Lys
NM_020631.6:c.1578C>G MANE Select NP_065682.2:p.Asn526Lys
NM_198681.4:c.1578C>G NP_941374.3:p.Asn526Lys