Canonical Allele Identifier: CA1144908299

Gene: PLEKHG5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6468075_6468078delinsGAGG , CM000663.2:g.6468075_6468078delinsGAGG	GRCh38
NC_000001.10:g.6528135_6528138delinsGAGG , CM000663.1:g.6528135_6528138delinsGAGG	GRCh37
NC_000001.9:g.6450722_6450725delinsGAGG	NCBI36
NG_007978.1:g.56932_56935delinsCCTC , LRG_262:g.56932_56935delinsCCTC
NG_029910.1:g.3118_3121delinsCCTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000340850.10:c.2758_2761delinsCCTC	ENSP00000344570.5:p.Pro920=
ENST00000377728.8:c.2758_2761delinsCCTC MANE Select	ENSP00000366957.3:p.Pro920=
ENST00000377740.5:c.2758_2761delinsCCTC	ENSP00000366969.4:p.Pro920=
ENST00000377748.6:c.2932_2935delinsCCTC	ENSP00000366977.2:p.Pro978=
ENST00000400913.6:c.2758_2761delinsCCTC	ENSP00000383704.1:p.Pro920=
ENST00000400915.8:c.2869_2872delinsCCTC	ENSP00000383706.4:p.Pro957=
ENST00000489097.6:n.3234_3237delinsCCTC
ENST00000535355.6:c.2965_2968delinsCCTC	ENSP00000441445.1:p.Pro989=
ENST00000537245.6:c.2869_2872delinsCCTC	ENSP00000439625.2:p.Pro957=
ENST00000673471.2:c.3055_3058delinsCCTC	ENSP00000500749.1:p.Pro1019=
ENST00000674790.1:c.*2970_*2973delinsCCTC	ENSP00000502815.1:n.*2970_*2973delinsCCTC
ENST00000675123.1:c.2250-185_2250-182delinsCCTC	ENSP00000502132.1:n.2250-185_2250-182delinsCCTC
ENST00000675548.1:c.*2586_*2589delinsCCTC	ENSP00000502684.1:n.*2586_*2589delinsCCTC
ENST00000675694.1:c.2758_2761delinsCCTC	ENSP00000501925.1:p.Pro920=
ENST00000675976.1:c.631_634delinsCCTC	ENSP00000501611.1:p.Pro211=
ENST00000340850.9:c.2758_2761delinsCCTC	ENSP00000344570.5:p.Pro920=
ENST00000377725.5:c.2737+21_2737+24delinsCCTC	ENSP00000366954.1:n.2737+21_2737+24delinsCCTC
ENST00000377728.7:c.2758_2761delinsCCTC	ENSP00000366957.3:p.Pro920=
ENST00000377732.5:c.2869_2872delinsCCTC	ENSP00000366961.1:p.Pro957=
ENST00000377740.4:c.2481-185_2481-182delinsCCTC	ENSP00000366969.3:n.2481-185_2481-182delinsCCTC
ENST00000377748.5:c.2989_2992delinsCCTC	ENSP00000366977.1:p.Pro997=
ENST00000400913.5:c.2758_2761delinsCCTC	ENSP00000383704.1:p.Pro920=
ENST00000400915.7:c.2926_2929delinsCCTC	ENSP00000383706.3:p.Pro976=
ENST00000487949.4:n.1960_1963delinsCCTC
ENST00000489097.5:n.3234_3237delinsCCTC
ENST00000535355.5:c.2965_2968delinsCCTC	ENSP00000441445.1:p.Pro989=
ENST00000537245.5:c.2995_2998delinsCCTC	ENSP00000439625.1:p.Pro999=
NM_001042663.1:c.2926_2929delinsCCTC	NP_001036128.1:p.Pro976=
NM_001042664.1:c.2758_2761delinsCCTC	NP_001036129.1:p.Pro920=
NM_001042665.1:c.2758_2761delinsCCTC	NP_001036130.1:p.Pro920=
NM_001265592.1:c.2995_2998delinsCCTC	NP_001252521.1:p.Pro999=
NM_001265593.1:c.2965_2968delinsCCTC	NP_001252522.1:p.Pro989=
NM_001265594.1:c.2737+21_2737+24delinsCCTC	NP_001252523.1:n.2737+21_2737+24delinsCCTC
NM_020631.4:c.2758_2761delinsCCTC	NP_065682.2:p.Pro920=
NM_198681.3:c.2989_2992delinsCCTC	NP_941374.2:p.Pro997=
NM_001042663.2:c.2926_2929delinsCCTC	NP_001036128.1:p.Pro976=
NM_001265594.2:c.2737+21_2737+24delinsCCTC	NP_001252523.1:n.2737+21_2737+24delinsCCTC
NM_020631.5:c.2758_2761delinsCCTC	NP_065682.2:p.Pro920=
NM_001042663.3:c.2869_2872delinsCCTC	NP_001036128.2:p.Pro957=
NM_001265592.2:c.2869_2872delinsCCTC	NP_001252521.2:p.Pro957=
NM_020631.6:c.2758_2761delinsCCTC MANE Select	NP_065682.2:p.Pro920=
NM_198681.4:c.2758_2761delinsCCTC	NP_941374.3:p.Pro920=