Canonical Allele Identifier: CA1151520584

Gene: PLEKHG5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6469157_6469160delinsCCTG , CM000663.2:g.6469157_6469160delinsCCTG	GRCh38
NC_000001.10:g.6529217_6529220delinsCCTG , CM000663.1:g.6529217_6529220delinsCCTG	GRCh37
NC_000001.9:g.6451804_6451807delinsCCTG	NCBI36
NG_007978.1:g.55850_55853delinsCAGG , LRG_262:g.55850_55853delinsCAGG
NG_029910.1:g.2036_2039delinsCAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.2131_2134delinsCAGG	ENSP00000344570.5:p.Gln711=
ENST00000377728.8:c.2131_2134delinsCAGG MANE Select	ENSP00000366957.3:p.Gln711=
ENST00000377740.5:c.2131_2134delinsCAGG	ENSP00000366969.4:p.Gln711=
ENST00000377748.6:c.2305_2308delinsCAGG	ENSP00000366977.2:p.Gln769=
ENST00000400913.6:c.2131_2134delinsCAGG	ENSP00000383704.1:p.Gln711=
ENST00000400915.8:c.2242_2245delinsCAGG	ENSP00000383706.4:p.Gln748=
ENST00000489097.6:n.2607_2610delinsCAGG
ENST00000535355.6:c.2338_2341delinsCAGG	ENSP00000441445.1:p.Gln780=
ENST00000537245.6:c.2242_2245delinsCAGG	ENSP00000439625.2:p.Gln748=
ENST00000673471.2:c.2428_2431delinsCAGG	ENSP00000500749.1:p.Gln810=
ENST00000674790.1:c.*2343_*2346delinsCAGG	ENSP00000502815.1:n.*2343_*2346delinsCAGG
ENST00000675123.1:c.2131_2134delinsCAGG	ENSP00000502132.1:p.Gln711=
ENST00000675139.1:n.202_205delinsCAGG
ENST00000675548.1:c.*1959_*1962delinsCAGG	ENSP00000502684.1:n.*1959_*1962delinsCAGG
ENST00000675694.1:c.2131_2134delinsCAGG	ENSP00000501925.1:p.Gln711=
ENST00000675976.1:c.4_7delinsCAGG	ENSP00000501611.1:p.Gln2=
ENST00000340850.9:c.2131_2134delinsCAGG	ENSP00000344570.5:p.Gln711=
ENST00000377725.5:c.2131_2134delinsCAGG	ENSP00000366954.1:p.Gln711=
ENST00000377728.7:c.2131_2134delinsCAGG	ENSP00000366957.3:p.Gln711=
ENST00000377732.5:c.2242_2245delinsCAGG	ENSP00000366961.1:p.Gln748=
ENST00000377740.4:c.2362_2365delinsCAGG	ENSP00000366969.3:p.Gln788=
ENST00000377748.5:c.2362_2365delinsCAGG	ENSP00000366977.1:p.Gln788=
ENST00000400913.5:c.2131_2134delinsCAGG	ENSP00000383704.1:p.Gln711=
ENST00000400915.7:c.2299_2302delinsCAGG	ENSP00000383706.3:p.Gln767=
ENST00000487949.4:n.1333_1336delinsCAGG
ENST00000489097.5:n.2607_2610delinsCAGG
ENST00000535355.5:c.2338_2341delinsCAGG	ENSP00000441445.1:p.Gln780=
ENST00000537245.5:c.2368_2371delinsCAGG	ENSP00000439625.1:p.Gln790=
NM_001042663.1:c.2299_2302delinsCAGG	NP_001036128.1:p.Gln767=
NM_001042664.1:c.2131_2134delinsCAGG	NP_001036129.1:p.Gln711=
NM_001042665.1:c.2131_2134delinsCAGG	NP_001036130.1:p.Gln711=
NM_001265592.1:c.2368_2371delinsCAGG	NP_001252521.1:p.Gln790=
NM_001265593.1:c.2338_2341delinsCAGG	NP_001252522.1:p.Gln780=
NM_001265594.1:c.2131_2134delinsCAGG	NP_001252523.1:p.Gln711=
NM_020631.4:c.2131_2134delinsCAGG	NP_065682.2:p.Gln711=
NM_198681.3:c.2362_2365delinsCAGG	NP_941374.2:p.Gln788=
NM_001042663.2:c.2299_2302delinsCAGG	NP_001036128.1:p.Gln767=
NM_001265594.2:c.2131_2134delinsCAGG	NP_001252523.1:p.Gln711=
NM_020631.5:c.2131_2134delinsCAGG	NP_065682.2:p.Gln711=
NM_001042663.3:c.2242_2245delinsCAGG	NP_001036128.2:p.Gln748=
NM_001265592.2:c.2242_2245delinsCAGG	NP_001252521.2:p.Gln748=
NM_020631.6:c.2131_2134delinsCAGG MANE Select	NP_065682.2:p.Gln711=
NM_198681.4:c.2131_2134delinsCAGG	NP_941374.3:p.Gln711=