Canonical Allele Identifier: CA2566457126

Gene: PLEKHG5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6470893_6470894insACA , CM000663.2:g.6470893_6470894insACA	GRCh38
NC_000001.10:g.6530953_6530954insACA , CM000663.1:g.6530953_6530954insACA	GRCh37
NC_000001.9:g.6453540_6453541insACA	NCBI36
NG_007978.1:g.54116_54117insTGT , LRG_262:g.54116_54117insTGT
NG_029910.1:g.302_303insTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.1393-10_1393-9insTGT	ENSP00000344570.5:n.1393-10_1393-9insTGT
ENST00000377728.8:c.1393-10_1393-9insTGT MANE Select	ENSP00000366957.3:n.1393-10_1393-9insTGT
ENST00000377740.5:c.1393-10_1393-9insTGT	ENSP00000366969.4:n.1393-10_1393-9insTGT
ENST00000377748.6:c.1567-10_1567-9insTGT	ENSP00000366977.2:n.1567-10_1567-9insTGT
ENST00000400913.6:c.1393-10_1393-9insTGT	ENSP00000383704.1:n.1393-10_1393-9insTGT
ENST00000400915.8:c.1504-10_1504-9insTGT	ENSP00000383706.4:n.1504-10_1504-9insTGT
ENST00000489097.6:n.1869-10_1869-9insTGT
ENST00000535355.6:c.1600-10_1600-9insTGT	ENSP00000441445.1:n.1600-10_1600-9insTGT
ENST00000537245.6:c.1504-10_1504-9insTGT	ENSP00000439625.2:n.1504-10_1504-9insTGT
ENST00000673471.2:c.1690-10_1690-9insTGT	ENSP00000500749.1:n.1690-10_1690-9insTGT
ENST00000674685.1:n.426-10_426-9insTGT
ENST00000674790.1:c.*1605-10_*1605-9insTGT	ENSP00000502815.1:n.*1605-10_*1605-9insTGT
ENST00000674943.1:n.45_46insTGT
ENST00000675123.1:c.1393-10_1393-9insTGT	ENSP00000502132.1:n.1393-10_1393-9insTGT
ENST00000675548.1:c.*1221-10_*1221-9insTGT	ENSP00000502684.1:n.*1221-10_*1221-9insTGT
ENST00000675694.1:c.1393-10_1393-9insTGT	ENSP00000501925.1:n.1393-10_1393-9insTGT
ENST00000340850.9:c.1393-10_1393-9insTGT	ENSP00000344570.5:n.1393-10_1393-9insTGT
ENST00000377725.5:c.1393-10_1393-9insTGT	ENSP00000366954.1:n.1393-10_1393-9insTGT
ENST00000377728.7:c.1393-10_1393-9insTGT	ENSP00000366957.3:n.1393-10_1393-9insTGT
ENST00000377732.5:c.1504-10_1504-9insTGT	ENSP00000366961.1:n.1504-10_1504-9insTGT
ENST00000377740.4:c.1624-10_1624-9insTGT	ENSP00000366969.3:n.1624-10_1624-9insTGT
ENST00000377748.5:c.1624-10_1624-9insTGT	ENSP00000366977.1:n.1624-10_1624-9insTGT
ENST00000400913.5:c.1393-10_1393-9insTGT	ENSP00000383704.1:n.1393-10_1393-9insTGT
ENST00000400915.7:c.1561-10_1561-9insTGT	ENSP00000383706.3:n.1561-10_1561-9insTGT
ENST00000487949.4:n.595-10_595-9insTGT
ENST00000489097.5:n.1869-10_1869-9insTGT
ENST00000535355.5:c.1600-10_1600-9insTGT	ENSP00000441445.1:n.1600-10_1600-9insTGT
ENST00000537245.5:c.1630-10_1630-9insTGT	ENSP00000439625.1:n.1630-10_1630-9insTGT
NM_001042663.1:c.1561-10_1561-9insTGT	NP_001036128.1:n.1561-10_1561-9insTGT
NM_001042664.1:c.1393-10_1393-9insTGT	NP_001036129.1:n.1393-10_1393-9insTGT
NM_001042665.1:c.1393-10_1393-9insTGT	NP_001036130.1:n.1393-10_1393-9insTGT
NM_001265592.1:c.1630-10_1630-9insTGT	NP_001252521.1:n.1630-10_1630-9insTGT
NM_001265593.1:c.1600-10_1600-9insTGT	NP_001252522.1:n.1600-10_1600-9insTGT
NM_001265594.1:c.1393-10_1393-9insTGT	NP_001252523.1:n.1393-10_1393-9insTGT
NM_020631.4:c.1393-10_1393-9insTGT	NP_065682.2:n.1393-10_1393-9insTGT
NM_198681.3:c.1624-10_1624-9insTGT	NP_941374.2:n.1624-10_1624-9insTGT
NM_001042663.2:c.1561-10_1561-9insTGT	NP_001036128.1:n.1561-10_1561-9insTGT
NM_001265594.2:c.1393-10_1393-9insTGT	NP_001252523.1:n.1393-10_1393-9insTGT
NM_020631.5:c.1393-10_1393-9insTGT	NP_065682.2:n.1393-10_1393-9insTGT
NM_001042663.3:c.1504-10_1504-9insTGT	NP_001036128.2:n.1504-10_1504-9insTGT
NM_001265592.2:c.1504-10_1504-9insTGT	NP_001252521.2:n.1504-10_1504-9insTGT
NM_020631.6:c.1393-10_1393-9insTGT MANE Select	NP_065682.2:n.1393-10_1393-9insTGT
NM_198681.4:c.1393-10_1393-9insTGT	NP_941374.3:n.1393-10_1393-9insTGT