Canonical Allele Identifier: CA1151514075

Gene: PLEKHG5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6477612_6477613delinsAG , CM000663.2:g.6477612_6477613delinsAG	GRCh38
NC_000001.10:g.6537672_6537673delinsAG , CM000663.1:g.6537672_6537673delinsAG	GRCh37
NC_000001.9:g.6460259_6460260delinsAG	NCBI36
NG_007978.1:g.47397_47398delinsCT , LRG_262:g.47397_47398delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.-42_-41delinsCT	ENSP00000344570.5:n.-42_-41delinsCT
ENST00000377728.8:c.-42_-41delinsCT MANE Select	ENSP00000366957.3:n.-42_-41delinsCT
ENST00000377740.5:c.-42_-41delinsCT	ENSP00000366969.4:n.-42_-41delinsCT
ENST00000377748.6:c.70_71delinsCT	ENSP00000366977.2:p.Leu24=
ENST00000400913.6:c.-42_-41delinsCT	ENSP00000383704.1:n.-42_-41delinsCT
ENST00000400915.8:c.70_71delinsCT	ENSP00000383706.4:p.Leu24=
ENST00000535355.6:c.166_167delinsCT	ENSP00000441445.1:p.Leu56=
ENST00000537245.6:c.70_71delinsCT	ENSP00000439625.2:p.Leu24=
ENST00000673471.2:c.256_257delinsCT	ENSP00000500749.1:p.Leu86=
ENST00000674790.1:c.*171_*172delinsCT	ENSP00000502815.1:n.*171_*172delinsCT
ENST00000674803.1:n.189_190delinsCT
ENST00000675093.1:c.-42_-41delinsCT	ENSP00000502687.1:n.-42_-41delinsCT
ENST00000675123.1:c.-42_-41delinsCT	ENSP00000502132.1:n.-42_-41delinsCT
ENST00000675548.1:c.144_145delinsCT	ENSP00000502684.1:p.Pro48=
ENST00000675655.1:n.165_166delinsCT
ENST00000675694.1:c.-42_-41delinsCT	ENSP00000501925.1:n.-42_-41delinsCT
ENST00000676287.1:c.-42_-41delinsCT	ENSP00000502810.1:n.-42_-41delinsCT
ENST00000676362.1:n.182_183delinsCT
ENST00000340850.9:c.-42_-41delinsCT	ENSP00000344570.5:n.-42_-41delinsCT
ENST00000377725.5:c.-42_-41delinsCT	ENSP00000366954.1:n.-42_-41delinsCT
ENST00000377728.7:c.-42_-41delinsCT	ENSP00000366957.3:n.-42_-41delinsCT
ENST00000377732.5:c.70_71delinsCT	ENSP00000366961.1:p.Leu24=
ENST00000377740.4:c.190_191delinsCT	ENSP00000366969.3:p.Leu64=
ENST00000377748.5:c.190_191delinsCT	ENSP00000366977.1:p.Leu64=
ENST00000400913.5:c.-42_-41delinsCT	ENSP00000383704.1:n.-42_-41delinsCT
ENST00000400915.7:c.127_128delinsCT	ENSP00000383706.3:p.Leu43=
ENST00000535355.5:c.166_167delinsCT	ENSP00000441445.1:p.Leu56=
ENST00000537245.5:c.196_197delinsCT	ENSP00000439625.1:p.Leu66=
NM_001042663.1:c.127_128delinsCT	NP_001036128.1:p.Leu43=
NM_001042664.1:c.-42_-41delinsCT	NP_001036129.1:n.-42_-41delinsCT
NM_001042665.1:c.-42_-41delinsCT	NP_001036130.1:n.-42_-41delinsCT
NM_001265592.1:c.196_197delinsCT	NP_001252521.1:p.Leu66=
NM_001265593.1:c.166_167delinsCT	NP_001252522.1:p.Leu56=
NM_001265594.1:c.-42_-41delinsCT	NP_001252523.1:n.-42_-41delinsCT
NM_020631.4:c.-42_-41delinsCT	NP_065682.2:n.-42_-41delinsCT
NM_198681.3:c.190_191delinsCT	NP_941374.2:p.Leu64=
NM_001042663.2:c.127_128delinsCT	NP_001036128.1:p.Leu43=
NM_001265594.2:c.-42_-41delinsCT	NP_001252523.1:n.-42_-41delinsCT
NM_020631.5:c.-42_-41delinsCT	NP_065682.2:n.-42_-41delinsCT
NM_001042663.3:c.70_71delinsCT	NP_001036128.2:p.Leu24=
NM_001265592.2:c.70_71delinsCT	NP_001252521.2:p.Leu24=
NM_020631.6:c.-42_-41delinsCT MANE Select	NP_065682.2:n.-42_-41delinsCT
NM_198681.4:c.-42_-41delinsCT	NP_941374.3:n.-42_-41delinsCT