Canonical Allele Identifier: CA1151517888

Gene: PLEKHG5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6468295_6468296delinsTG , CM000663.2:g.6468295_6468296delinsTG	GRCh38
NC_000001.10:g.6528355_6528356delinsTG , CM000663.1:g.6528355_6528356delinsTG	GRCh37
NC_000001.9:g.6450942_6450943delinsTG	NCBI36
NG_007978.1:g.56714_56715delinsCA , LRG_262:g.56714_56715delinsCA
NG_029910.1:g.2900_2901delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.2540_2541delinsCA	ENSP00000344570.5:p.Pro847=
ENST00000377728.8:c.2540_2541delinsCA MANE Select	ENSP00000366957.3:p.Pro847=
ENST00000377740.5:c.2540_2541delinsCA	ENSP00000366969.4:p.Pro847=
ENST00000377748.6:c.2714_2715delinsCA	ENSP00000366977.2:p.Pro905=
ENST00000400913.6:c.2540_2541delinsCA	ENSP00000383704.1:p.Pro847=
ENST00000400915.8:c.2651_2652delinsCA	ENSP00000383706.4:p.Pro884=
ENST00000489097.6:n.3016_3017delinsCA
ENST00000535355.6:c.2747_2748delinsCA	ENSP00000441445.1:p.Pro916=
ENST00000537245.6:c.2651_2652delinsCA	ENSP00000439625.2:p.Pro884=
ENST00000673471.2:c.2837_2838delinsCA	ENSP00000500749.1:p.Pro946=
ENST00000674790.1:c.*2752_*2753delinsCA	ENSP00000502815.1:n.*2752_*2753delinsCA
ENST00000675123.1:c.2250-403_2250-402delinsCA	ENSP00000502132.1:n.2250-403_2250-402delinsCA
ENST00000675548.1:c.*2368_*2369delinsCA	ENSP00000502684.1:n.*2368_*2369delinsCA
ENST00000675694.1:c.2540_2541delinsCA	ENSP00000501925.1:p.Pro847=
ENST00000675976.1:c.413_414delinsCA	ENSP00000501611.1:p.Pro138=
ENST00000340850.9:c.2540_2541delinsCA	ENSP00000344570.5:p.Pro847=
ENST00000377725.5:c.2540_2541delinsCA	ENSP00000366954.1:p.Pro847=
ENST00000377728.7:c.2540_2541delinsCA	ENSP00000366957.3:p.Pro847=
ENST00000377732.5:c.2651_2652delinsCA	ENSP00000366961.1:p.Pro884=
ENST00000377740.4:c.2481-403_2481-402delinsCA	ENSP00000366969.3:n.2481-403_2481-402delinsCA
ENST00000377748.5:c.2771_2772delinsCA	ENSP00000366977.1:p.Pro924=
ENST00000400913.5:c.2540_2541delinsCA	ENSP00000383704.1:p.Pro847=
ENST00000400915.7:c.2708_2709delinsCA	ENSP00000383706.3:p.Pro903=
ENST00000487949.4:n.1742_1743delinsCA
ENST00000489097.5:n.3016_3017delinsCA
ENST00000535355.5:c.2747_2748delinsCA	ENSP00000441445.1:p.Pro916=
ENST00000537245.5:c.2777_2778delinsCA	ENSP00000439625.1:p.Pro926=
NM_001042663.1:c.2708_2709delinsCA	NP_001036128.1:p.Pro903=
NM_001042664.1:c.2540_2541delinsCA	NP_001036129.1:p.Pro847=
NM_001042665.1:c.2540_2541delinsCA	NP_001036130.1:p.Pro847=
NM_001265592.1:c.2777_2778delinsCA	NP_001252521.1:p.Pro926=
NM_001265593.1:c.2747_2748delinsCA	NP_001252522.1:p.Pro916=
NM_001265594.1:c.2540_2541delinsCA	NP_001252523.1:p.Pro847=
NM_020631.4:c.2540_2541delinsCA	NP_065682.2:p.Pro847=
NM_198681.3:c.2771_2772delinsCA	NP_941374.2:p.Pro924=
NM_001042663.2:c.2708_2709delinsCA	NP_001036128.1:p.Pro903=
NM_001265594.2:c.2540_2541delinsCA	NP_001252523.1:p.Pro847=
NM_020631.5:c.2540_2541delinsCA	NP_065682.2:p.Pro847=
NM_001042663.3:c.2651_2652delinsCA	NP_001036128.2:p.Pro884=
NM_001265592.2:c.2651_2652delinsCA	NP_001252521.2:p.Pro884=
NM_020631.6:c.2540_2541delinsCA MANE Select	NP_065682.2:p.Pro847=
NM_198681.4:c.2540_2541delinsCA	NP_941374.3:p.Pro847=