Canonical Allele Identifier: CA1148472387

Gene: PLEKHG5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6469083G= , CM000663.2:g.6469083G=	GRCh38
NC_000001.10:g.6529143G= , CM000663.1:g.6529143G=	GRCh37
NC_000001.9:g.6451730G=	NCBI36
NG_007978.1:g.55927C= , LRG_262:g.55927C=
NG_029910.1:g.2113C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.2208C=	ENSP00000344570.5:p.Thr736=
ENST00000377728.8:c.2208C= MANE Select	ENSP00000366957.3:p.Thr736=
ENST00000377740.5:c.2208C=	ENSP00000366969.4:p.Thr736=
ENST00000377748.6:c.2382C=	ENSP00000366977.2:p.Thr794=
ENST00000400913.6:c.2208C=	ENSP00000383704.1:p.Thr736=
ENST00000400915.8:c.2319C=	ENSP00000383706.4:p.Thr773=
ENST00000489097.6:n.2684C=
ENST00000535355.6:c.2415C=	ENSP00000441445.1:p.Thr805=
ENST00000537245.6:c.2319C=	ENSP00000439625.2:p.Thr773=
ENST00000673471.2:c.2505C=	ENSP00000500749.1:p.Thr835=
ENST00000674790.1:c.*2420C=	ENSP00000502815.1:n.*2420C=
ENST00000675123.1:c.2208C=	ENSP00000502132.1:p.Thr736=
ENST00000675139.1:n.279C=
ENST00000675548.1:c.*2036C=	ENSP00000502684.1:n.*2036C=
ENST00000675694.1:c.2208C=	ENSP00000501925.1:p.Thr736=
ENST00000675976.1:c.81C=	ENSP00000501611.1:p.Thr27=
ENST00000340850.9:c.2208C=	ENSP00000344570.5:p.Thr736=
ENST00000377725.5:c.2208C=	ENSP00000366954.1:p.Thr736=
ENST00000377728.7:c.2208C=	ENSP00000366957.3:p.Thr736=
ENST00000377732.5:c.2319C=	ENSP00000366961.1:p.Thr773=
ENST00000377740.4:c.2439C=	ENSP00000366969.3:p.Thr813=
ENST00000377748.5:c.2439C=	ENSP00000366977.1:p.Thr813=
ENST00000400913.5:c.2208C=	ENSP00000383704.1:p.Thr736=
ENST00000400915.7:c.2376C=	ENSP00000383706.3:p.Thr792=
ENST00000487949.4:n.1410C=
ENST00000489097.5:n.2684C=
ENST00000535355.5:c.2415C=	ENSP00000441445.1:p.Thr805=
ENST00000537245.5:c.2445C=	ENSP00000439625.1:p.Thr815=
NM_001042663.1:c.2376C=	NP_001036128.1:p.Thr792=
NM_001042664.1:c.2208C=	NP_001036129.1:p.Thr736=
NM_001042665.1:c.2208C=	NP_001036130.1:p.Thr736=
NM_001265592.1:c.2445C=	NP_001252521.1:p.Thr815=
NM_001265593.1:c.2415C=	NP_001252522.1:p.Thr805=
NM_001265594.1:c.2208C=	NP_001252523.1:p.Thr736=
NM_020631.4:c.2208C=	NP_065682.2:p.Thr736=
NM_198681.3:c.2439C=	NP_941374.2:p.Thr813=
NM_001042663.2:c.2376C=	NP_001036128.1:p.Thr792=
NM_001265594.2:c.2208C=	NP_001252523.1:p.Thr736=
NM_020631.5:c.2208C=	NP_065682.2:p.Thr736=
NM_001042663.3:c.2319C=	NP_001036128.2:p.Thr773=
NM_001265592.2:c.2319C=	NP_001252521.2:p.Thr773=
NM_020631.6:c.2208C= MANE Select	NP_065682.2:p.Thr736=
NM_198681.4:c.2208C=	NP_941374.3:p.Thr736=