Canonical Allele Identifier: CA1151520186

Gene: PLEKHG5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6469120_6469123delinsCCTT , CM000663.2:g.6469120_6469123delinsCCTT	GRCh38
NC_000001.10:g.6529180_6529183delinsCCTT , CM000663.1:g.6529180_6529183delinsCCTT	GRCh37
NC_000001.9:g.6451767_6451770delinsCCTT	NCBI36
NG_007978.1:g.55887_55890delinsAAGG , LRG_262:g.55887_55890delinsAAGG
NG_029910.1:g.2073_2076delinsAAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.2168_2171delinsAAGG	ENSP00000344570.5:p.Glu723=
ENST00000377728.8:c.2168_2171delinsAAGG MANE Select	ENSP00000366957.3:p.Glu723=
ENST00000377740.5:c.2168_2171delinsAAGG	ENSP00000366969.4:p.Glu723=
ENST00000377748.6:c.2342_2345delinsAAGG	ENSP00000366977.2:p.Glu781=
ENST00000400913.6:c.2168_2171delinsAAGG	ENSP00000383704.1:p.Glu723=
ENST00000400915.8:c.2279_2282delinsAAGG	ENSP00000383706.4:p.Glu760=
ENST00000489097.6:n.2644_2647delinsAAGG
ENST00000535355.6:c.2375_2378delinsAAGG	ENSP00000441445.1:p.Glu792=
ENST00000537245.6:c.2279_2282delinsAAGG	ENSP00000439625.2:p.Glu760=
ENST00000673471.2:c.2465_2468delinsAAGG	ENSP00000500749.1:p.Glu822=
ENST00000674790.1:c.*2380_*2383delinsAAGG	ENSP00000502815.1:n.*2380_*2383delinsAAGG
ENST00000675123.1:c.2168_2171delinsAAGG	ENSP00000502132.1:p.Glu723=
ENST00000675139.1:n.239_242delinsAAGG
ENST00000675548.1:c.*1996_*1999delinsAAGG	ENSP00000502684.1:n.*1996_*1999delinsAAGG
ENST00000675694.1:c.2168_2171delinsAAGG	ENSP00000501925.1:p.Glu723=
ENST00000675976.1:c.41_44delinsAAGG	ENSP00000501611.1:p.Glu14=
ENST00000340850.9:c.2168_2171delinsAAGG	ENSP00000344570.5:p.Glu723=
ENST00000377725.5:c.2168_2171delinsAAGG	ENSP00000366954.1:p.Glu723=
ENST00000377728.7:c.2168_2171delinsAAGG	ENSP00000366957.3:p.Glu723=
ENST00000377732.5:c.2279_2282delinsAAGG	ENSP00000366961.1:p.Glu760=
ENST00000377740.4:c.2399_2402delinsAAGG	ENSP00000366969.3:p.Glu800=
ENST00000377748.5:c.2399_2402delinsAAGG	ENSP00000366977.1:p.Glu800=
ENST00000400913.5:c.2168_2171delinsAAGG	ENSP00000383704.1:p.Glu723=
ENST00000400915.7:c.2336_2339delinsAAGG	ENSP00000383706.3:p.Glu779=
ENST00000487949.4:n.1370_1373delinsAAGG
ENST00000489097.5:n.2644_2647delinsAAGG
ENST00000535355.5:c.2375_2378delinsAAGG	ENSP00000441445.1:p.Glu792=
ENST00000537245.5:c.2405_2408delinsAAGG	ENSP00000439625.1:p.Glu802=
NM_001042663.1:c.2336_2339delinsAAGG	NP_001036128.1:p.Glu779=
NM_001042664.1:c.2168_2171delinsAAGG	NP_001036129.1:p.Glu723=
NM_001042665.1:c.2168_2171delinsAAGG	NP_001036130.1:p.Glu723=
NM_001265592.1:c.2405_2408delinsAAGG	NP_001252521.1:p.Glu802=
NM_001265593.1:c.2375_2378delinsAAGG	NP_001252522.1:p.Glu792=
NM_001265594.1:c.2168_2171delinsAAGG	NP_001252523.1:p.Glu723=
NM_020631.4:c.2168_2171delinsAAGG	NP_065682.2:p.Glu723=
NM_198681.3:c.2399_2402delinsAAGG	NP_941374.2:p.Glu800=
NM_001042663.2:c.2336_2339delinsAAGG	NP_001036128.1:p.Glu779=
NM_001265594.2:c.2168_2171delinsAAGG	NP_001252523.1:p.Glu723=
NM_020631.5:c.2168_2171delinsAAGG	NP_065682.2:p.Glu723=
NM_001042663.3:c.2279_2282delinsAAGG	NP_001036128.2:p.Glu760=
NM_001265592.2:c.2279_2282delinsAAGG	NP_001252521.2:p.Glu760=
NM_020631.6:c.2168_2171delinsAAGG MANE Select	NP_065682.2:p.Glu723=
NM_198681.4:c.2168_2171delinsAAGG	NP_941374.3:p.Glu723=