Canonical Allele Identifier: CA1151520367

Gene: PLEKHG5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6469129_6469130delinsTC , CM000663.2:g.6469129_6469130delinsTC	GRCh38
NC_000001.10:g.6529189_6529190delinsTC , CM000663.1:g.6529189_6529190delinsTC	GRCh37
NC_000001.9:g.6451776_6451777delinsTC	NCBI36
NG_007978.1:g.55880_55881delinsGA , LRG_262:g.55880_55881delinsGA
NG_029910.1:g.2066_2067delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.2161_2162delinsGA	ENSP00000344570.5:p.Glu721=
ENST00000377728.8:c.2161_2162delinsGA MANE Select	ENSP00000366957.3:p.Glu721=
ENST00000377740.5:c.2161_2162delinsGA	ENSP00000366969.4:p.Glu721=
ENST00000377748.6:c.2335_2336delinsGA	ENSP00000366977.2:p.Glu779=
ENST00000400913.6:c.2161_2162delinsGA	ENSP00000383704.1:p.Glu721=
ENST00000400915.8:c.2272_2273delinsGA	ENSP00000383706.4:p.Glu758=
ENST00000489097.6:n.2637_2638delinsGA
ENST00000535355.6:c.2368_2369delinsGA	ENSP00000441445.1:p.Glu790=
ENST00000537245.6:c.2272_2273delinsGA	ENSP00000439625.2:p.Glu758=
ENST00000673471.2:c.2458_2459delinsGA	ENSP00000500749.1:p.Glu820=
ENST00000674790.1:c.*2373_*2374delinsGA	ENSP00000502815.1:n.*2373_*2374delinsGA
ENST00000675123.1:c.2161_2162delinsGA	ENSP00000502132.1:p.Glu721=
ENST00000675139.1:n.232_233delinsGA
ENST00000675548.1:c.*1989_*1990delinsGA	ENSP00000502684.1:n.*1989_*1990delinsGA
ENST00000675694.1:c.2161_2162delinsGA	ENSP00000501925.1:p.Glu721=
ENST00000675976.1:c.34_35delinsGA	ENSP00000501611.1:p.Glu12=
ENST00000340850.9:c.2161_2162delinsGA	ENSP00000344570.5:p.Glu721=
ENST00000377725.5:c.2161_2162delinsGA	ENSP00000366954.1:p.Glu721=
ENST00000377728.7:c.2161_2162delinsGA	ENSP00000366957.3:p.Glu721=
ENST00000377732.5:c.2272_2273delinsGA	ENSP00000366961.1:p.Glu758=
ENST00000377740.4:c.2392_2393delinsGA	ENSP00000366969.3:p.Glu798=
ENST00000377748.5:c.2392_2393delinsGA	ENSP00000366977.1:p.Glu798=
ENST00000400913.5:c.2161_2162delinsGA	ENSP00000383704.1:p.Glu721=
ENST00000400915.7:c.2329_2330delinsGA	ENSP00000383706.3:p.Glu777=
ENST00000487949.4:n.1363_1364delinsGA
ENST00000489097.5:n.2637_2638delinsGA
ENST00000535355.5:c.2368_2369delinsGA	ENSP00000441445.1:p.Glu790=
ENST00000537245.5:c.2398_2399delinsGA	ENSP00000439625.1:p.Glu800=
NM_001042663.1:c.2329_2330delinsGA	NP_001036128.1:p.Glu777=
NM_001042664.1:c.2161_2162delinsGA	NP_001036129.1:p.Glu721=
NM_001042665.1:c.2161_2162delinsGA	NP_001036130.1:p.Glu721=
NM_001265592.1:c.2398_2399delinsGA	NP_001252521.1:p.Glu800=
NM_001265593.1:c.2368_2369delinsGA	NP_001252522.1:p.Glu790=
NM_001265594.1:c.2161_2162delinsGA	NP_001252523.1:p.Glu721=
NM_020631.4:c.2161_2162delinsGA	NP_065682.2:p.Glu721=
NM_198681.3:c.2392_2393delinsGA	NP_941374.2:p.Glu798=
NM_001042663.2:c.2329_2330delinsGA	NP_001036128.1:p.Glu777=
NM_001265594.2:c.2161_2162delinsGA	NP_001252523.1:p.Glu721=
NM_020631.5:c.2161_2162delinsGA	NP_065682.2:p.Glu721=
NM_001042663.3:c.2272_2273delinsGA	NP_001036128.2:p.Glu758=
NM_001265592.2:c.2272_2273delinsGA	NP_001252521.2:p.Glu758=
NM_020631.6:c.2161_2162delinsGA MANE Select	NP_065682.2:p.Glu721=
NM_198681.4:c.2161_2162delinsGA	NP_941374.3:p.Glu721=