Canonical Allele Identifier: CA1151513432

Gene: PLEKHG5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6477329_6477330delinsAG , CM000663.2:g.6477329_6477330delinsAG	GRCh38
NC_000001.10:g.6537389_6537390delinsAG , CM000663.1:g.6537389_6537390delinsAG	GRCh37
NC_000001.9:g.6459976_6459977delinsAG	NCBI36
NG_007978.1:g.47680_47681delinsCT , LRG_262:g.47680_47681delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.43+199_43+200delinsCT	ENSP00000344570.5:n.43+199_43+200delinsCT
ENST00000377728.8:c.43+199_43+200delinsCT MANE Select	ENSP00000366957.3:n.43+199_43+200delinsCT
ENST00000377740.5:c.43+199_43+200delinsCT	ENSP00000366969.4:n.43+199_43+200delinsCT
ENST00000377748.6:c.154+199_154+200delinsCT	ENSP00000366977.2:n.154+199_154+200delinsCT
ENST00000400913.6:c.43+199_43+200delinsCT	ENSP00000383704.1:n.43+199_43+200delinsCT
ENST00000400915.8:c.154+199_154+200delinsCT	ENSP00000383706.4:n.154+199_154+200delinsCT
ENST00000489097.6:n.60+199_60+200delinsCT
ENST00000535355.6:c.250+199_250+200delinsCT	ENSP00000441445.1:n.250+199_250+200delinsCT
ENST00000537245.6:c.154+199_154+200delinsCT	ENSP00000439625.2:n.154+199_154+200delinsCT
ENST00000673471.2:c.340+199_340+200delinsCT	ENSP00000500749.1:n.340+199_340+200delinsCT
ENST00000674790.1:c.*255+199_*255+200delinsCT	ENSP00000502815.1:n.*255+199_*255+200delinsCT
ENST00000674803.1:n.273+199_273+200delinsCT
ENST00000675093.1:c.43+199_43+200delinsCT	ENSP00000502687.1:n.43+199_43+200delinsCT
ENST00000675123.1:c.43+199_43+200delinsCT	ENSP00000502132.1:n.43+199_43+200delinsCT
ENST00000675548.1:c.228+199_228+200delinsCT	ENSP00000502684.1:n.228+199_228+200delinsCT
ENST00000675655.1:n.249+199_249+200delinsCT
ENST00000675694.1:c.43+199_43+200delinsCT	ENSP00000501925.1:n.43+199_43+200delinsCT
ENST00000676287.1:c.43+199_43+200delinsCT	ENSP00000502810.1:n.43+199_43+200delinsCT
ENST00000676362.1:n.266+199_266+200delinsCT
ENST00000340850.9:c.43+199_43+200delinsCT	ENSP00000344570.5:n.43+199_43+200delinsCT
ENST00000377725.5:c.43+199_43+200delinsCT	ENSP00000366954.1:n.43+199_43+200delinsCT
ENST00000377728.7:c.43+199_43+200delinsCT	ENSP00000366957.3:n.43+199_43+200delinsCT
ENST00000377732.5:c.154+199_154+200delinsCT	ENSP00000366961.1:n.154+199_154+200delinsCT
ENST00000377740.4:c.274+199_274+200delinsCT	ENSP00000366969.3:n.274+199_274+200delinsCT
ENST00000377748.5:c.274+199_274+200delinsCT	ENSP00000366977.1:n.274+199_274+200delinsCT
ENST00000400913.5:c.43+199_43+200delinsCT	ENSP00000383704.1:n.43+199_43+200delinsCT
ENST00000400915.7:c.211+199_211+200delinsCT	ENSP00000383706.3:n.211+199_211+200delinsCT
ENST00000489097.5:n.60+199_60+200delinsCT
ENST00000535355.5:c.250+199_250+200delinsCT	ENSP00000441445.1:n.250+199_250+200delinsCT
ENST00000537245.5:c.280+199_280+200delinsCT	ENSP00000439625.1:n.280+199_280+200delinsCT
NM_001042663.1:c.211+199_211+200delinsCT	NP_001036128.1:n.211+199_211+200delinsCT
NM_001042664.1:c.43+199_43+200delinsCT	NP_001036129.1:n.43+199_43+200delinsCT
NM_001042665.1:c.43+199_43+200delinsCT	NP_001036130.1:n.43+199_43+200delinsCT
NM_001265592.1:c.280+199_280+200delinsCT	NP_001252521.1:n.280+199_280+200delinsCT
NM_001265593.1:c.250+199_250+200delinsCT	NP_001252522.1:n.250+199_250+200delinsCT
NM_001265594.1:c.43+199_43+200delinsCT	NP_001252523.1:n.43+199_43+200delinsCT
NM_020631.4:c.43+199_43+200delinsCT	NP_065682.2:n.43+199_43+200delinsCT
NM_198681.3:c.274+199_274+200delinsCT	NP_941374.2:n.274+199_274+200delinsCT
NM_001042663.2:c.211+199_211+200delinsCT	NP_001036128.1:n.211+199_211+200delinsCT
NM_001265594.2:c.43+199_43+200delinsCT	NP_001252523.1:n.43+199_43+200delinsCT
NM_020631.5:c.43+199_43+200delinsCT	NP_065682.2:n.43+199_43+200delinsCT
NM_001042663.3:c.154+199_154+200delinsCT	NP_001036128.2:n.154+199_154+200delinsCT
NM_001265592.2:c.154+199_154+200delinsCT	NP_001252521.2:n.154+199_154+200delinsCT
NM_020631.6:c.43+199_43+200delinsCT MANE Select	NP_065682.2:n.43+199_43+200delinsCT
NM_198681.4:c.43+199_43+200delinsCT	NP_941374.3:n.43+199_43+200delinsCT