Canonical Allele Identifier: CA1151524194

Gene: PLEKHG5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6470537_6470539delinsACC , CM000663.2:g.6470537_6470539delinsACC	GRCh38
NC_000001.10:g.6530597_6530599delinsACC , CM000663.1:g.6530597_6530599delinsACC	GRCh37
NC_000001.9:g.6453184_6453186delinsACC	NCBI36
NG_007978.1:g.54471_54473delinsGGT , LRG_262:g.54471_54473delinsGGT
NG_029910.1:g.657_659delinsGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.1647_1649delinsGGT	ENSP00000344570.5:p.Glu549=
ENST00000377728.8:c.1647_1649delinsGGT MANE Select	ENSP00000366957.3:p.Glu549=
ENST00000377740.5:c.1647_1649delinsGGT	ENSP00000366969.4:p.Glu549=
ENST00000377748.6:c.1821_1823delinsGGT	ENSP00000366977.2:p.Glu607=
ENST00000400913.6:c.1647_1649delinsGGT	ENSP00000383704.1:p.Glu549=
ENST00000400915.8:c.1758_1760delinsGGT	ENSP00000383706.4:p.Glu586=
ENST00000489097.6:n.2123_2125delinsGGT
ENST00000535355.6:c.1854_1856delinsGGT	ENSP00000441445.1:p.Glu618=
ENST00000537245.6:c.1758_1760delinsGGT	ENSP00000439625.2:p.Glu586=
ENST00000673471.2:c.1944_1946delinsGGT	ENSP00000500749.1:p.Glu648=
ENST00000674790.1:c.*1859_*1861delinsGGT	ENSP00000502815.1:n.*1859_*1861delinsGGT
ENST00000674943.1:n.309_311delinsGGT
ENST00000675123.1:c.1647_1649delinsGGT	ENSP00000502132.1:p.Glu549=
ENST00000675548.1:c.*1475_*1477delinsGGT	ENSP00000502684.1:n.*1475_*1477delinsGGT
ENST00000675694.1:c.1647_1649delinsGGT	ENSP00000501925.1:p.Glu549=
ENST00000676401.1:n.194_196delinsGGT
ENST00000340850.9:c.1647_1649delinsGGT	ENSP00000344570.5:p.Glu549=
ENST00000377725.5:c.1647_1649delinsGGT	ENSP00000366954.1:p.Glu549=
ENST00000377728.7:c.1647_1649delinsGGT	ENSP00000366957.3:p.Glu549=
ENST00000377732.5:c.1758_1760delinsGGT	ENSP00000366961.1:p.Glu586=
ENST00000377740.4:c.1878_1880delinsGGT	ENSP00000366969.3:p.Glu626=
ENST00000377748.5:c.1878_1880delinsGGT	ENSP00000366977.1:p.Glu626=
ENST00000400913.5:c.1647_1649delinsGGT	ENSP00000383704.1:p.Glu549=
ENST00000400915.7:c.1815_1817delinsGGT	ENSP00000383706.3:p.Glu605=
ENST00000487949.4:n.849_851delinsGGT
ENST00000489097.5:n.2123_2125delinsGGT
ENST00000535355.5:c.1854_1856delinsGGT	ENSP00000441445.1:p.Glu618=
ENST00000537245.5:c.1884_1886delinsGGT	ENSP00000439625.1:p.Glu628=
NM_001042663.1:c.1815_1817delinsGGT	NP_001036128.1:p.Glu605=
NM_001042664.1:c.1647_1649delinsGGT	NP_001036129.1:p.Glu549=
NM_001042665.1:c.1647_1649delinsGGT	NP_001036130.1:p.Glu549=
NM_001265592.1:c.1884_1886delinsGGT	NP_001252521.1:p.Glu628=
NM_001265593.1:c.1854_1856delinsGGT	NP_001252522.1:p.Glu618=
NM_001265594.1:c.1647_1649delinsGGT	NP_001252523.1:p.Glu549=
NM_020631.4:c.1647_1649delinsGGT	NP_065682.2:p.Glu549=
NM_198681.3:c.1878_1880delinsGGT	NP_941374.2:p.Glu626=
NM_001042663.2:c.1815_1817delinsGGT	NP_001036128.1:p.Glu605=
NM_001265594.2:c.1647_1649delinsGGT	NP_001252523.1:p.Glu549=
NM_020631.5:c.1647_1649delinsGGT	NP_065682.2:p.Glu549=
NM_001042663.3:c.1758_1760delinsGGT	NP_001036128.2:p.Glu586=
NM_001265592.2:c.1758_1760delinsGGT	NP_001252521.2:p.Glu586=
NM_020631.6:c.1647_1649delinsGGT MANE Select	NP_065682.2:p.Glu549=
NM_198681.4:c.1647_1649delinsGGT	NP_941374.3:p.Glu549=