Canonical Allele Identifier: CA1151520575

Gene: PLEKHG5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6469155_6469164delinsCTCCTGCTCA , CM000663.2:g.6469155_6469164delinsCTCCTGCTCA	GRCh38
NC_000001.10:g.6529215_6529224delinsCTCCTGCTCA , CM000663.1:g.6529215_6529224delinsCTCCTGCTCA	GRCh37
NC_000001.9:g.6451802_6451811delinsCTCCTGCTCA	NCBI36
NG_007978.1:g.55846_55855delinsTGAGCAGGAG , LRG_262:g.55846_55855delinsTGAGCAGGAG
NG_029910.1:g.2032_2041delinsTGAGCAGGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.2127_2136delinsTGAGCAGGAG	ENSP00000344570.5:p.Asp709=
ENST00000377728.8:c.2127_2136delinsTGAGCAGGAG MANE Select	ENSP00000366957.3:p.Asp709=
ENST00000377740.5:c.2127_2136delinsTGAGCAGGAG	ENSP00000366969.4:p.Asp709=
ENST00000377748.6:c.2301_2310delinsTGAGCAGGAG	ENSP00000366977.2:p.Asp767=
ENST00000400913.6:c.2127_2136delinsTGAGCAGGAG	ENSP00000383704.1:p.Asp709=
ENST00000400915.8:c.2238_2247delinsTGAGCAGGAG	ENSP00000383706.4:p.Asp746=
ENST00000489097.6:n.2603_2612delinsTGAGCAGGAG
ENST00000535355.6:c.2334_2343delinsTGAGCAGGAG	ENSP00000441445.1:p.Asp778=
ENST00000537245.6:c.2238_2247delinsTGAGCAGGAG	ENSP00000439625.2:p.Asp746=
ENST00000673471.2:c.2424_2433delinsTGAGCAGGAG	ENSP00000500749.1:p.Asp808=
ENST00000674790.1:c.*2339_*2348delinsTGAGCAGGAG	ENSP00000502815.1:n.*2339_*2348delinsTGAGCAGGAG
ENST00000675123.1:c.2127_2136delinsTGAGCAGGAG	ENSP00000502132.1:p.Asp709=
ENST00000675139.1:n.198_207delinsTGAGCAGGAG
ENST00000675548.1:c.*1955_*1964delinsTGAGCAGGAG	ENSP00000502684.1:n.*1955_*1964delinsTGAGCAGGAG
ENST00000675694.1:c.2127_2136delinsTGAGCAGGAG	ENSP00000501925.1:p.Asp709=
ENST00000340850.9:c.2127_2136delinsTGAGCAGGAG	ENSP00000344570.5:p.Asp709=
ENST00000377725.5:c.2127_2136delinsTGAGCAGGAG	ENSP00000366954.1:p.Asp709=
ENST00000377728.7:c.2127_2136delinsTGAGCAGGAG	ENSP00000366957.3:p.Asp709=
ENST00000377732.5:c.2238_2247delinsTGAGCAGGAG	ENSP00000366961.1:p.Asp746=
ENST00000377740.4:c.2358_2367delinsTGAGCAGGAG	ENSP00000366969.3:p.Asp786=
ENST00000377748.5:c.2358_2367delinsTGAGCAGGAG	ENSP00000366977.1:p.Asp786=
ENST00000400913.5:c.2127_2136delinsTGAGCAGGAG	ENSP00000383704.1:p.Asp709=
ENST00000400915.7:c.2295_2304delinsTGAGCAGGAG	ENSP00000383706.3:p.Asp765=
ENST00000487949.4:n.1329_1338delinsTGAGCAGGAG
ENST00000489097.5:n.2603_2612delinsTGAGCAGGAG
ENST00000535355.5:c.2334_2343delinsTGAGCAGGAG	ENSP00000441445.1:p.Asp778=
ENST00000537245.5:c.2364_2373delinsTGAGCAGGAG	ENSP00000439625.1:p.Asp788=
NM_001042663.1:c.2295_2304delinsTGAGCAGGAG	NP_001036128.1:p.Asp765=
NM_001042664.1:c.2127_2136delinsTGAGCAGGAG	NP_001036129.1:p.Asp709=
NM_001042665.1:c.2127_2136delinsTGAGCAGGAG	NP_001036130.1:p.Asp709=
NM_001265592.1:c.2364_2373delinsTGAGCAGGAG	NP_001252521.1:p.Asp788=
NM_001265593.1:c.2334_2343delinsTGAGCAGGAG	NP_001252522.1:p.Asp778=
NM_001265594.1:c.2127_2136delinsTGAGCAGGAG	NP_001252523.1:p.Asp709=
NM_020631.4:c.2127_2136delinsTGAGCAGGAG	NP_065682.2:p.Asp709=
NM_198681.3:c.2358_2367delinsTGAGCAGGAG	NP_941374.2:p.Asp786=
NM_001042663.2:c.2295_2304delinsTGAGCAGGAG	NP_001036128.1:p.Asp765=
NM_001265594.2:c.2127_2136delinsTGAGCAGGAG	NP_001252523.1:p.Asp709=
NM_020631.5:c.2127_2136delinsTGAGCAGGAG	NP_065682.2:p.Asp709=
NM_001042663.3:c.2238_2247delinsTGAGCAGGAG	NP_001036128.2:p.Asp746=
NM_001265592.2:c.2238_2247delinsTGAGCAGGAG	NP_001252521.2:p.Asp746=
NM_020631.6:c.2127_2136delinsTGAGCAGGAG MANE Select	NP_065682.2:p.Asp709=
NM_198681.4:c.2127_2136delinsTGAGCAGGAG	NP_941374.3:p.Asp709=