Canonical Allele Identifier: CA1151507761

Gene: PLEKHG5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6474866_6474867delinsAC , CM000663.2:g.6474866_6474867delinsAC	GRCh38
NC_000001.10:g.6534926_6534927delinsAC , CM000663.1:g.6534926_6534927delinsAC	GRCh37
NC_000001.9:g.6457513_6457514delinsAC	NCBI36
NG_007978.1:g.50143_50144delinsGT , LRG_262:g.50143_50144delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.302+180_302+181delinsGT	ENSP00000344570.5:n.302+180_302+181delinsGT
ENST00000377728.8:c.302+180_302+181delinsGT MANE Select	ENSP00000366957.3:n.302+180_302+181delinsGT
ENST00000377740.5:c.302+180_302+181delinsGT	ENSP00000366969.4:n.302+180_302+181delinsGT
ENST00000377748.6:c.476+180_476+181delinsGT	ENSP00000366977.2:n.476+180_476+181delinsGT
ENST00000400913.6:c.302+180_302+181delinsGT	ENSP00000383704.1:n.302+180_302+181delinsGT
ENST00000400915.8:c.413+180_413+181delinsGT	ENSP00000383706.4:n.413+180_413+181delinsGT
ENST00000489097.6:n.499_500delinsGT
ENST00000535355.6:c.509+180_509+181delinsGT	ENSP00000441445.1:n.509+180_509+181delinsGT
ENST00000537245.6:c.413+180_413+181delinsGT	ENSP00000439625.2:n.413+180_413+181delinsGT
ENST00000673471.2:c.599+180_599+181delinsGT	ENSP00000500749.1:n.599+180_599+181delinsGT
ENST00000674790.1:c.*514+180_*514+181delinsGT	ENSP00000502815.1:n.*514+180_*514+181delinsGT
ENST00000675093.1:c.302+180_302+181delinsGT	ENSP00000502687.1:n.302+180_302+181delinsGT
ENST00000675123.1:c.302+180_302+181delinsGT	ENSP00000502132.1:n.302+180_302+181delinsGT
ENST00000675548.1:c.*130+180_*130+181delinsGT	ENSP00000502684.1:n.*130+180_*130+181delinsGT
ENST00000675694.1:c.302+180_302+181delinsGT	ENSP00000501925.1:n.302+180_302+181delinsGT
ENST00000676255.1:c.129-35_129-34delinsGT	ENSP00000502459.1:n.129-35_129-34delinsGT
ENST00000676287.1:c.302+180_302+181delinsGT	ENSP00000502810.1:n.302+180_302+181delinsGT
ENST00000340850.9:c.302+180_302+181delinsGT	ENSP00000344570.5:n.302+180_302+181delinsGT
ENST00000377725.5:c.302+180_302+181delinsGT	ENSP00000366954.1:n.302+180_302+181delinsGT
ENST00000377728.7:c.302+180_302+181delinsGT	ENSP00000366957.3:n.302+180_302+181delinsGT
ENST00000377732.5:c.413+180_413+181delinsGT	ENSP00000366961.1:n.413+180_413+181delinsGT
ENST00000377740.4:c.533+180_533+181delinsGT	ENSP00000366969.3:n.533+180_533+181delinsGT
ENST00000377748.5:c.533+180_533+181delinsGT	ENSP00000366977.1:n.533+180_533+181delinsGT
ENST00000400913.5:c.302+180_302+181delinsGT	ENSP00000383704.1:n.302+180_302+181delinsGT
ENST00000400915.7:c.470+180_470+181delinsGT	ENSP00000383706.3:n.470+180_470+181delinsGT
ENST00000489097.5:n.499_500delinsGT
ENST00000535355.5:c.509+180_509+181delinsGT	ENSP00000441445.1:n.509+180_509+181delinsGT
ENST00000537245.5:c.539+180_539+181delinsGT	ENSP00000439625.1:n.539+180_539+181delinsGT
NM_001042663.1:c.470+180_470+181delinsGT	NP_001036128.1:n.470+180_470+181delinsGT
NM_001042664.1:c.302+180_302+181delinsGT	NP_001036129.1:n.302+180_302+181delinsGT
NM_001042665.1:c.302+180_302+181delinsGT	NP_001036130.1:n.302+180_302+181delinsGT
NM_001265592.1:c.539+180_539+181delinsGT	NP_001252521.1:n.539+180_539+181delinsGT
NM_001265593.1:c.509+180_509+181delinsGT	NP_001252522.1:n.509+180_509+181delinsGT
NM_001265594.1:c.302+180_302+181delinsGT	NP_001252523.1:n.302+180_302+181delinsGT
NM_020631.4:c.302+180_302+181delinsGT	NP_065682.2:n.302+180_302+181delinsGT
NM_198681.3:c.533+180_533+181delinsGT	NP_941374.2:n.533+180_533+181delinsGT
NM_001042663.2:c.470+180_470+181delinsGT	NP_001036128.1:n.470+180_470+181delinsGT
NM_001265594.2:c.302+180_302+181delinsGT	NP_001252523.1:n.302+180_302+181delinsGT
NM_020631.5:c.302+180_302+181delinsGT	NP_065682.2:n.302+180_302+181delinsGT
NM_001042663.3:c.413+180_413+181delinsGT	NP_001036128.2:n.413+180_413+181delinsGT
NM_001265592.2:c.413+180_413+181delinsGT	NP_001252521.2:n.413+180_413+181delinsGT
NM_020631.6:c.302+180_302+181delinsGT MANE Select	NP_065682.2:n.302+180_302+181delinsGT
NM_198681.4:c.302+180_302+181delinsGT	NP_941374.3:n.302+180_302+181delinsGT