Canonical Allele Identifier: CA2740090576

Gene: PLEKHG5

Linked Data

• ClinVar Variation Id: 2947865
• ClinVar RCV Id: RCV003804495

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6469138_6469142del , CM000663.2:g.6469138_6469142del	GRCh38
NC_000001.10:g.6529198_6529202del , CM000663.1:g.6529198_6529202del	GRCh37
NC_000001.9:g.6451785_6451789del	NCBI36
NG_007978.1:g.55869_55873del , LRG_262:g.55869_55873del
NG_029910.1:g.2055_2059del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.2150_2154del	ENSP00000344570.5:p.Glu717GlyfsTer?
ENST00000377728.8:c.2150_2154del MANE Select	ENSP00000366957.3:p.Glu717GlyfsTer?
ENST00000377740.5:c.2150_2154del	ENSP00000366969.4:p.Glu717GlyfsTer?
ENST00000377748.6:c.2324_2328del	ENSP00000366977.2:p.Glu775GlyfsTer?
ENST00000400913.6:c.2150_2154del	ENSP00000383704.1:p.Glu717GlyfsTer?
ENST00000400915.8:c.2261_2265del	ENSP00000383706.4:p.Glu754GlyfsTer?
ENST00000489097.6:n.2626_2630del
ENST00000535355.6:c.2357_2361del	ENSP00000441445.1:p.Glu786GlyfsTer?
ENST00000537245.6:c.2261_2265del	ENSP00000439625.2:p.Glu754GlyfsTer?
ENST00000673471.2:c.2447_2451del	ENSP00000500749.1:p.Glu816GlyfsTer?
ENST00000674790.1:c.*2362_*2366del	ENSP00000502815.1:n.*2362_*2366del
ENST00000675123.1:c.2150_2154del	ENSP00000502132.1:p.Glu717GlyfsTer?
ENST00000675139.1:n.221_225del
ENST00000675548.1:c.*1978_*1982del	ENSP00000502684.1:n.*1978_*1982del
ENST00000675694.1:c.2150_2154del	ENSP00000501925.1:p.Glu717GlyfsTer?
ENST00000675976.1:c.23_27del	ENSP00000501611.1:p.Glu8GlyfsTer?
ENST00000340850.9:c.2150_2154del	ENSP00000344570.5:p.Glu717GlyfsTer?
ENST00000377725.5:c.2150_2154del	ENSP00000366954.1:p.Glu717GlyfsTer?
ENST00000377728.7:c.2150_2154del	ENSP00000366957.3:p.Glu717GlyfsTer?
ENST00000377732.5:c.2261_2265del	ENSP00000366961.1:p.Glu754GlyfsTer?
ENST00000377740.4:c.2381_2385del	ENSP00000366969.3:p.Glu794GlyfsTer?
ENST00000377748.5:c.2381_2385del	ENSP00000366977.1:p.Glu794GlyfsTer?
ENST00000400913.5:c.2150_2154del	ENSP00000383704.1:p.Glu717GlyfsTer?
ENST00000400915.7:c.2318_2322del	ENSP00000383706.3:p.Glu773GlyfsTer?
ENST00000487949.4:n.1352_1356del
ENST00000489097.5:n.2626_2630del
ENST00000535355.5:c.2357_2361del	ENSP00000441445.1:p.Glu786GlyfsTer?
ENST00000537245.5:c.2387_2391del	ENSP00000439625.1:p.Glu796GlyfsTer?
NM_001042663.1:c.2318_2322del	NP_001036128.1:p.Glu773GlyfsTer?
NM_001042664.1:c.2150_2154del	NP_001036129.1:p.Glu717GlyfsTer?
NM_001042665.1:c.2150_2154del	NP_001036130.1:p.Glu717GlyfsTer?
NM_001265592.1:c.2387_2391del	NP_001252521.1:p.Glu796GlyfsTer?
NM_001265593.1:c.2357_2361del	NP_001252522.1:p.Glu786GlyfsTer?
NM_001265594.1:c.2150_2154del	NP_001252523.1:p.Glu717GlyfsTer?
NM_020631.4:c.2150_2154del	NP_065682.2:p.Glu717GlyfsTer?
NM_198681.3:c.2381_2385del	NP_941374.2:p.Glu794GlyfsTer?
NM_001042663.2:c.2318_2322del	NP_001036128.1:p.Glu773GlyfsTer?
NM_001265594.2:c.2150_2154del	NP_001252523.1:p.Glu717GlyfsTer?
NM_020631.5:c.2150_2154del	NP_065682.2:p.Glu717GlyfsTer?
NM_001042663.3:c.2261_2265del	NP_001036128.2:p.Glu754GlyfsTer?
NM_001265592.2:c.2261_2265del	NP_001252521.2:p.Glu754GlyfsTer?
NM_020631.6:c.2150_2154del MANE Select	NP_065682.2:p.Glu717GlyfsTer?
NM_198681.4:c.2150_2154del	NP_941374.3:p.Glu717GlyfsTer?