Canonical Allele Identifier: CA1151502224

Gene: PLEKHG5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6472692_6472693delinsAC , CM000663.2:g.6472692_6472693delinsAC	GRCh38
NC_000001.10:g.6532752_6532753delinsAC , CM000663.1:g.6532752_6532753delinsAC	GRCh37
NC_000001.9:g.6455339_6455340delinsAC	NCBI36
NG_007978.1:g.52317_52318delinsGT , LRG_262:g.52317_52318delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.985-71_985-70delinsGT	ENSP00000344570.5:n.985-71_985-70delinsGT
ENST00000377728.8:c.985-71_985-70delinsGT MANE Select	ENSP00000366957.3:n.985-71_985-70delinsGT
ENST00000377740.5:c.985-71_985-70delinsGT	ENSP00000366969.4:n.985-71_985-70delinsGT
ENST00000377748.6:c.1159-71_1159-70delinsGT	ENSP00000366977.2:n.1159-71_1159-70delinsGT
ENST00000400913.6:c.985-71_985-70delinsGT	ENSP00000383704.1:n.985-71_985-70delinsGT
ENST00000400915.8:c.1096-71_1096-70delinsGT	ENSP00000383706.4:n.1096-71_1096-70delinsGT
ENST00000489097.6:n.1461-71_1461-70delinsGT
ENST00000535355.6:c.1192-71_1192-70delinsGT	ENSP00000441445.1:n.1192-71_1192-70delinsGT
ENST00000537245.6:c.1096-71_1096-70delinsGT	ENSP00000439625.2:n.1096-71_1096-70delinsGT
ENST00000673471.2:c.1282-71_1282-70delinsGT	ENSP00000500749.1:n.1282-71_1282-70delinsGT
ENST00000674790.1:c.*1197-71_*1197-70delinsGT	ENSP00000502815.1:n.*1197-71_*1197-70delinsGT
ENST00000675123.1:c.985-71_985-70delinsGT	ENSP00000502132.1:n.985-71_985-70delinsGT
ENST00000675548.1:c.*813-71_*813-70delinsGT	ENSP00000502684.1:n.*813-71_*813-70delinsGT
ENST00000675694.1:c.985-71_985-70delinsGT	ENSP00000501925.1:n.985-71_985-70delinsGT
ENST00000340850.9:c.985-71_985-70delinsGT	ENSP00000344570.5:n.985-71_985-70delinsGT
ENST00000377725.5:c.985-71_985-70delinsGT	ENSP00000366954.1:n.985-71_985-70delinsGT
ENST00000377728.7:c.985-71_985-70delinsGT	ENSP00000366957.3:n.985-71_985-70delinsGT
ENST00000377732.5:c.1096-71_1096-70delinsGT	ENSP00000366961.1:n.1096-71_1096-70delinsGT
ENST00000377740.4:c.1216-71_1216-70delinsGT	ENSP00000366969.3:n.1216-71_1216-70delinsGT
ENST00000377748.5:c.1216-71_1216-70delinsGT	ENSP00000366977.1:n.1216-71_1216-70delinsGT
ENST00000400913.5:c.985-71_985-70delinsGT	ENSP00000383704.1:n.985-71_985-70delinsGT
ENST00000400915.7:c.1153-71_1153-70delinsGT	ENSP00000383706.3:n.1153-71_1153-70delinsGT
ENST00000489097.5:n.1461-71_1461-70delinsGT
ENST00000535355.5:c.1192-71_1192-70delinsGT	ENSP00000441445.1:n.1192-71_1192-70delinsGT
ENST00000537245.5:c.1222-71_1222-70delinsGT	ENSP00000439625.1:n.1222-71_1222-70delinsGT
NM_001042663.1:c.1153-71_1153-70delinsGT	NP_001036128.1:n.1153-71_1153-70delinsGT
NM_001042664.1:c.985-71_985-70delinsGT	NP_001036129.1:n.985-71_985-70delinsGT
NM_001042665.1:c.985-71_985-70delinsGT	NP_001036130.1:n.985-71_985-70delinsGT
NM_001265592.1:c.1222-71_1222-70delinsGT	NP_001252521.1:n.1222-71_1222-70delinsGT
NM_001265593.1:c.1192-71_1192-70delinsGT	NP_001252522.1:n.1192-71_1192-70delinsGT
NM_001265594.1:c.985-71_985-70delinsGT	NP_001252523.1:n.985-71_985-70delinsGT
NM_020631.4:c.985-71_985-70delinsGT	NP_065682.2:n.985-71_985-70delinsGT
NM_198681.3:c.1216-71_1216-70delinsGT	NP_941374.2:n.1216-71_1216-70delinsGT
NM_001042663.2:c.1153-71_1153-70delinsGT	NP_001036128.1:n.1153-71_1153-70delinsGT
NM_001265594.2:c.985-71_985-70delinsGT	NP_001252523.1:n.985-71_985-70delinsGT
NM_020631.5:c.985-71_985-70delinsGT	NP_065682.2:n.985-71_985-70delinsGT
NM_001042663.3:c.1096-71_1096-70delinsGT	NP_001036128.2:n.1096-71_1096-70delinsGT
NM_001265592.2:c.1096-71_1096-70delinsGT	NP_001252521.2:n.1096-71_1096-70delinsGT
NM_020631.6:c.985-71_985-70delinsGT MANE Select	NP_065682.2:n.985-71_985-70delinsGT
NM_198681.4:c.985-71_985-70delinsGT	NP_941374.3:n.985-71_985-70delinsGT