Canonical Allele Identifier: CA1151514054

Gene: PLEKHG5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6477606_6477607delinsAG , CM000663.2:g.6477606_6477607delinsAG	GRCh38
NC_000001.10:g.6537666_6537667delinsAG , CM000663.1:g.6537666_6537667delinsAG	GRCh37
NC_000001.9:g.6460253_6460254delinsAG	NCBI36
NG_007978.1:g.47403_47404delinsCT , LRG_262:g.47403_47404delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.-36_-35delinsCT	ENSP00000344570.5:n.-36_-35delinsCT
ENST00000377728.8:c.-36_-35delinsCT MANE Select	ENSP00000366957.3:n.-36_-35delinsCT
ENST00000377740.5:c.-36_-35delinsCT	ENSP00000366969.4:n.-36_-35delinsCT
ENST00000377748.6:c.76_77delinsCT	ENSP00000366977.2:p.Leu26=
ENST00000400913.6:c.-36_-35delinsCT	ENSP00000383704.1:n.-36_-35delinsCT
ENST00000400915.8:c.76_77delinsCT	ENSP00000383706.4:p.Leu26=
ENST00000535355.6:c.172_173delinsCT	ENSP00000441445.1:p.Leu58=
ENST00000537245.6:c.76_77delinsCT	ENSP00000439625.2:p.Leu26=
ENST00000673471.2:c.262_263delinsCT	ENSP00000500749.1:p.Leu88=
ENST00000674790.1:c.*177_*178delinsCT	ENSP00000502815.1:n.*177_*178delinsCT
ENST00000674803.1:n.195_196delinsCT
ENST00000675093.1:c.-36_-35delinsCT	ENSP00000502687.1:n.-36_-35delinsCT
ENST00000675123.1:c.-36_-35delinsCT	ENSP00000502132.1:n.-36_-35delinsCT
ENST00000675548.1:c.150_151delinsCT	ENSP00000502684.1:p.Thr50=
ENST00000675655.1:n.171_172delinsCT
ENST00000675694.1:c.-36_-35delinsCT	ENSP00000501925.1:n.-36_-35delinsCT
ENST00000676287.1:c.-36_-35delinsCT	ENSP00000502810.1:n.-36_-35delinsCT
ENST00000676362.1:n.188_189delinsCT
ENST00000340850.9:c.-36_-35delinsCT	ENSP00000344570.5:n.-36_-35delinsCT
ENST00000377725.5:c.-36_-35delinsCT	ENSP00000366954.1:n.-36_-35delinsCT
ENST00000377728.7:c.-36_-35delinsCT	ENSP00000366957.3:n.-36_-35delinsCT
ENST00000377732.5:c.76_77delinsCT	ENSP00000366961.1:p.Leu26=
ENST00000377740.4:c.196_197delinsCT	ENSP00000366969.3:p.Leu66=
ENST00000377748.5:c.196_197delinsCT	ENSP00000366977.1:p.Leu66=
ENST00000400913.5:c.-36_-35delinsCT	ENSP00000383704.1:n.-36_-35delinsCT
ENST00000400915.7:c.133_134delinsCT	ENSP00000383706.3:p.Leu45=
ENST00000535355.5:c.172_173delinsCT	ENSP00000441445.1:p.Leu58=
ENST00000537245.5:c.202_203delinsCT	ENSP00000439625.1:p.Leu68=
NM_001042663.1:c.133_134delinsCT	NP_001036128.1:p.Leu45=
NM_001042664.1:c.-36_-35delinsCT	NP_001036129.1:n.-36_-35delinsCT
NM_001042665.1:c.-36_-35delinsCT	NP_001036130.1:n.-36_-35delinsCT
NM_001265592.1:c.202_203delinsCT	NP_001252521.1:p.Leu68=
NM_001265593.1:c.172_173delinsCT	NP_001252522.1:p.Leu58=
NM_001265594.1:c.-36_-35delinsCT	NP_001252523.1:n.-36_-35delinsCT
NM_020631.4:c.-36_-35delinsCT	NP_065682.2:n.-36_-35delinsCT
NM_198681.3:c.196_197delinsCT	NP_941374.2:p.Leu66=
NM_001042663.2:c.133_134delinsCT	NP_001036128.1:p.Leu45=
NM_001265594.2:c.-36_-35delinsCT	NP_001252523.1:n.-36_-35delinsCT
NM_020631.5:c.-36_-35delinsCT	NP_065682.2:n.-36_-35delinsCT
NM_001042663.3:c.76_77delinsCT	NP_001036128.2:p.Leu26=
NM_001265592.2:c.76_77delinsCT	NP_001252521.2:p.Leu26=
NM_020631.6:c.-36_-35delinsCT MANE Select	NP_065682.2:n.-36_-35delinsCT
NM_198681.4:c.-36_-35delinsCT	NP_941374.3:n.-36_-35delinsCT