Canonical Allele Identifier: CA2840114419

Gene: PLEKHG5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6473990_6473991insCT , CM000663.2:g.6473990_6473991insCT	GRCh38
NC_000001.10:g.6534050_6534051insCT , CM000663.1:g.6534050_6534051insCT	GRCh37
NC_000001.9:g.6456637_6456638insCT	NCBI36
NG_007978.1:g.51019_51020insAG , LRG_262:g.51019_51020insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.591+22_591+23insAG	ENSP00000344570.5:n.591+22_591+23insAG
ENST00000377728.8:c.591+22_591+23insAG MANE Select	ENSP00000366957.3:n.591+22_591+23insAG
ENST00000377740.5:c.591+22_591+23insAG	ENSP00000366969.4:n.591+22_591+23insAG
ENST00000377748.6:c.765+22_765+23insAG	ENSP00000366977.2:n.765+22_765+23insAG
ENST00000400913.6:c.591+22_591+23insAG	ENSP00000383704.1:n.591+22_591+23insAG
ENST00000400915.8:c.702+22_702+23insAG	ENSP00000383706.4:n.702+22_702+23insAG
ENST00000489097.6:n.1067+22_1067+23insAG
ENST00000535355.6:c.798+22_798+23insAG	ENSP00000441445.1:n.798+22_798+23insAG
ENST00000537245.6:c.702+22_702+23insAG	ENSP00000439625.2:n.702+22_702+23insAG
ENST00000673471.2:c.888+22_888+23insAG	ENSP00000500749.1:n.888+22_888+23insAG
ENST00000674790.1:c.*803+22_*803+23insAG	ENSP00000502815.1:n.*803+22_*803+23insAG
ENST00000675123.1:c.591+22_591+23insAG	ENSP00000502132.1:n.591+22_591+23insAG
ENST00000675548.1:c.*419+22_*419+23insAG	ENSP00000502684.1:n.*419+22_*419+23insAG
ENST00000675694.1:c.591+22_591+23insAG	ENSP00000501925.1:n.591+22_591+23insAG
ENST00000340850.9:c.591+22_591+23insAG	ENSP00000344570.5:n.591+22_591+23insAG
ENST00000377725.5:c.591+22_591+23insAG	ENSP00000366954.1:n.591+22_591+23insAG
ENST00000377728.7:c.591+22_591+23insAG	ENSP00000366957.3:n.591+22_591+23insAG
ENST00000377732.5:c.702+22_702+23insAG	ENSP00000366961.1:n.702+22_702+23insAG
ENST00000377740.4:c.822+22_822+23insAG	ENSP00000366969.3:n.822+22_822+23insAG
ENST00000377748.5:c.822+22_822+23insAG	ENSP00000366977.1:n.822+22_822+23insAG
ENST00000400913.5:c.591+22_591+23insAG	ENSP00000383704.1:n.591+22_591+23insAG
ENST00000400915.7:c.759+22_759+23insAG	ENSP00000383706.3:n.759+22_759+23insAG
ENST00000489097.5:n.1067+22_1067+23insAG
ENST00000535355.5:c.798+22_798+23insAG	ENSP00000441445.1:n.798+22_798+23insAG
ENST00000537245.5:c.828+22_828+23insAG	ENSP00000439625.1:n.828+22_828+23insAG
NM_001042663.1:c.759+22_759+23insAG	NP_001036128.1:n.759+22_759+23insAG
NM_001042664.1:c.591+22_591+23insAG	NP_001036129.1:n.591+22_591+23insAG
NM_001042665.1:c.591+22_591+23insAG	NP_001036130.1:n.591+22_591+23insAG
NM_001265592.1:c.828+22_828+23insAG	NP_001252521.1:n.828+22_828+23insAG
NM_001265593.1:c.798+22_798+23insAG	NP_001252522.1:n.798+22_798+23insAG
NM_001265594.1:c.591+22_591+23insAG	NP_001252523.1:n.591+22_591+23insAG
NM_020631.4:c.591+22_591+23insAG	NP_065682.2:n.591+22_591+23insAG
NM_198681.3:c.822+22_822+23insAG	NP_941374.2:n.822+22_822+23insAG
NM_001042663.2:c.759+22_759+23insAG	NP_001036128.1:n.759+22_759+23insAG
NM_001265594.2:c.591+22_591+23insAG	NP_001252523.1:n.591+22_591+23insAG
NM_020631.5:c.591+22_591+23insAG	NP_065682.2:n.591+22_591+23insAG
NM_001042663.3:c.702+22_702+23insAG	NP_001036128.2:n.702+22_702+23insAG
NM_001265592.2:c.702+22_702+23insAG	NP_001252521.2:n.702+22_702+23insAG
NM_020631.6:c.591+22_591+23insAG MANE Select	NP_065682.2:n.591+22_591+23insAG
NM_198681.4:c.591+22_591+23insAG	NP_941374.3:n.591+22_591+23insAG