Canonical Allele Identifier: CA2574194622
Gene: PLEKHG5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.6470676del , CM000663.2:g.6470676del GRCh38
NC_000001.10:g.6530736del , CM000663.1:g.6530736del GRCh37
NC_000001.9:g.6453323del NCBI36
NG_007978.1:g.54336del , LRG_262:g.54336del
NG_029910.1:g.522del

Transcript Alleles

HGVS Amino-acid Change
ENST00000340850.10:c.1543-31del ENSP00000344570.5:n.1543-31del
ENST00000377728.8:c.1543-31del MANE Select ENSP00000366957.3:n.1543-31del
ENST00000377740.5:c.1543-31del ENSP00000366969.4:n.1543-31del
ENST00000377748.6:c.1717-31del ENSP00000366977.2:n.1717-31del
ENST00000400913.6:c.1543-31del ENSP00000383704.1:n.1543-31del
ENST00000400915.8:c.1654-31del ENSP00000383706.4:n.1654-31del
ENST00000489097.6:n.2019-31del
ENST00000535355.6:c.1750-31del ENSP00000441445.1:n.1750-31del
ENST00000537245.6:c.1654-31del ENSP00000439625.2:n.1654-31del
ENST00000673471.2:c.1840-31del ENSP00000500749.1:n.1840-31del
ENST00000674685.1:n.576-31del
ENST00000674790.1:c.*1755-31del ENSP00000502815.1:n.*1755-31del
ENST00000674943.1:n.205-31del
ENST00000675123.1:c.1543-31del ENSP00000502132.1:n.1543-31del
ENST00000675548.1:c.*1371-31del ENSP00000502684.1:n.*1371-31del
ENST00000675694.1:c.1543-31del ENSP00000501925.1:n.1543-31del
ENST00000676401.1:n.59del
ENST00000340850.9:c.1543-31del ENSP00000344570.5:n.1543-31del
ENST00000377725.5:c.1543-31del ENSP00000366954.1:n.1543-31del
ENST00000377728.7:c.1543-31del ENSP00000366957.3:n.1543-31del
ENST00000377732.5:c.1654-31del ENSP00000366961.1:n.1654-31del
ENST00000377740.4:c.1774-31del ENSP00000366969.3:n.1774-31del
ENST00000377748.5:c.1774-31del ENSP00000366977.1:n.1774-31del
ENST00000400913.5:c.1543-31del ENSP00000383704.1:n.1543-31del
ENST00000400915.7:c.1711-31del ENSP00000383706.3:n.1711-31del
ENST00000487949.4:n.745-31del
ENST00000489097.5:n.2019-31del
ENST00000535355.5:c.1750-31del ENSP00000441445.1:n.1750-31del
ENST00000537245.5:c.1780-31del ENSP00000439625.1:n.1780-31del
NM_001042663.1:c.1711-31del NP_001036128.1:n.1711-31del
NM_001042664.1:c.1543-31del NP_001036129.1:n.1543-31del
NM_001042665.1:c.1543-31del NP_001036130.1:n.1543-31del
NM_001265592.1:c.1780-31del NP_001252521.1:n.1780-31del
NM_001265593.1:c.1750-31del NP_001252522.1:n.1750-31del
NM_001265594.1:c.1543-31del NP_001252523.1:n.1543-31del
NM_020631.4:c.1543-31del NP_065682.2:n.1543-31del
NM_198681.3:c.1774-31del NP_941374.2:n.1774-31del
NM_001042663.2:c.1711-31del NP_001036128.1:n.1711-31del
NM_001265594.2:c.1543-31del NP_001252523.1:n.1543-31del
NM_020631.5:c.1543-31del NP_065682.2:n.1543-31del
NM_001042663.3:c.1654-31del NP_001036128.2:n.1654-31del
NM_001265592.2:c.1654-31del NP_001252521.2:n.1654-31del
NM_020631.6:c.1543-31del MANE Select NP_065682.2:n.1543-31del
NM_198681.4:c.1543-31del NP_941374.3:n.1543-31del