Canonical Allele Identifier: CA2642975259

Gene: PLEKHG5

Linked Data

• gnomAD v4: 1-6469149-T-TGCTCA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6469149_6469150insGCTCA , CM000663.2:g.6469149_6469150insGCTCA	GRCh38
NC_000001.10:g.6529209_6529210insGCTCA , CM000663.1:g.6529209_6529210insGCTCA	GRCh37
NC_000001.9:g.6451796_6451797insGCTCA	NCBI36
NG_007978.1:g.55860_55861insTGAGC , LRG_262:g.55860_55861insTGAGC
NG_029910.1:g.2046_2047insTGAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.2141_2142insTGAGC	ENSP00000344570.5:p.Glu714AspfsTer?
ENST00000377728.8:c.2141_2142insTGAGC MANE Select	ENSP00000366957.3:p.Glu714AspfsTer?
ENST00000377740.5:c.2141_2142insTGAGC	ENSP00000366969.4:p.Glu714AspfsTer?
ENST00000377748.6:c.2315_2316insTGAGC	ENSP00000366977.2:p.Glu772AspfsTer?
ENST00000400913.6:c.2141_2142insTGAGC	ENSP00000383704.1:p.Glu714AspfsTer?
ENST00000400915.8:c.2252_2253insTGAGC	ENSP00000383706.4:p.Glu751AspfsTer?
ENST00000489097.6:n.2617_2618insTGAGC
ENST00000535355.6:c.2348_2349insTGAGC	ENSP00000441445.1:p.Glu783AspfsTer?
ENST00000537245.6:c.2252_2253insTGAGC	ENSP00000439625.2:p.Glu751AspfsTer?
ENST00000673471.2:c.2438_2439insTGAGC	ENSP00000500749.1:p.Glu813AspfsTer?
ENST00000674790.1:c.*2353_*2354insTGAGC	ENSP00000502815.1:n.*2353_*2354insTGAGC
ENST00000675123.1:c.2141_2142insTGAGC	ENSP00000502132.1:p.Glu714AspfsTer?
ENST00000675139.1:n.212_213insTGAGC
ENST00000675548.1:c.*1969_*1970insTGAGC	ENSP00000502684.1:n.*1969_*1970insTGAGC
ENST00000675694.1:c.2141_2142insTGAGC	ENSP00000501925.1:p.Glu714AspfsTer?
ENST00000675976.1:c.14_15insTGAGC	ENSP00000501611.1:p.Glu5AspfsTer?
ENST00000340850.9:c.2141_2142insTGAGC	ENSP00000344570.5:p.Glu714AspfsTer?
ENST00000377725.5:c.2141_2142insTGAGC	ENSP00000366954.1:p.Glu714AspfsTer?
ENST00000377728.7:c.2141_2142insTGAGC	ENSP00000366957.3:p.Glu714AspfsTer?
ENST00000377732.5:c.2252_2253insTGAGC	ENSP00000366961.1:p.Glu751AspfsTer?
ENST00000377740.4:c.2372_2373insTGAGC	ENSP00000366969.3:p.Glu791AspfsTer?
ENST00000377748.5:c.2372_2373insTGAGC	ENSP00000366977.1:p.Glu791AspfsTer?
ENST00000400913.5:c.2141_2142insTGAGC	ENSP00000383704.1:p.Glu714AspfsTer?
ENST00000400915.7:c.2309_2310insTGAGC	ENSP00000383706.3:p.Glu770AspfsTer?
ENST00000487949.4:n.1343_1344insTGAGC
ENST00000489097.5:n.2617_2618insTGAGC
ENST00000535355.5:c.2348_2349insTGAGC	ENSP00000441445.1:p.Glu783AspfsTer?
ENST00000537245.5:c.2378_2379insTGAGC	ENSP00000439625.1:p.Glu793AspfsTer?
NM_001042663.1:c.2309_2310insTGAGC	NP_001036128.1:p.Glu770AspfsTer?
NM_001042664.1:c.2141_2142insTGAGC	NP_001036129.1:p.Glu714AspfsTer?
NM_001042665.1:c.2141_2142insTGAGC	NP_001036130.1:p.Glu714AspfsTer?
NM_001265592.1:c.2378_2379insTGAGC	NP_001252521.1:p.Glu793AspfsTer?
NM_001265593.1:c.2348_2349insTGAGC	NP_001252522.1:p.Glu783AspfsTer?
NM_001265594.1:c.2141_2142insTGAGC	NP_001252523.1:p.Glu714AspfsTer?
NM_020631.4:c.2141_2142insTGAGC	NP_065682.2:p.Glu714AspfsTer?
NM_198681.3:c.2372_2373insTGAGC	NP_941374.2:p.Glu791AspfsTer?
NM_001042663.2:c.2309_2310insTGAGC	NP_001036128.1:p.Glu770AspfsTer?
NM_001265594.2:c.2141_2142insTGAGC	NP_001252523.1:p.Glu714AspfsTer?
NM_020631.5:c.2141_2142insTGAGC	NP_065682.2:p.Glu714AspfsTer?
NM_001042663.3:c.2252_2253insTGAGC	NP_001036128.2:p.Glu751AspfsTer?
NM_001265592.2:c.2252_2253insTGAGC	NP_001252521.2:p.Glu751AspfsTer?
NM_020631.6:c.2141_2142insTGAGC MANE Select	NP_065682.2:p.Glu714AspfsTer?
NM_198681.4:c.2141_2142insTGAGC	NP_941374.3:p.Glu714AspfsTer?