Canonical Allele Identifier: CA415833789

Gene: PLEKHG5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6473365A>C , CM000663.2:g.6473365A>C	GRCh38
NC_000001.10:g.6533425A>C , CM000663.1:g.6533425A>C	GRCh37
NC_000001.9:g.6456012A>C	NCBI36
NG_007978.1:g.51645T>G , LRG_262:g.51645T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.681T>G	ENSP00000344570.5:p.Ser227=
ENST00000377728.8:c.681T>G MANE Select	ENSP00000366957.3:p.Ser227=
ENST00000377740.5:c.681T>G	ENSP00000366969.4:p.Ser227=
ENST00000377748.6:c.855T>G	ENSP00000366977.2:p.Ser285=
ENST00000400913.6:c.681T>G	ENSP00000383704.1:p.Ser227=
ENST00000400915.8:c.792T>G	ENSP00000383706.4:p.Ser264=
ENST00000489097.6:n.1157T>G
ENST00000535355.6:c.888T>G	ENSP00000441445.1:p.Ser296=
ENST00000537245.6:c.792T>G	ENSP00000439625.2:p.Ser264=
ENST00000673471.2:c.978T>G	ENSP00000500749.1:p.Ser326=
ENST00000674790.1:c.*893T>G	ENSP00000502815.1:n.*893T>G
ENST00000675123.1:c.681T>G	ENSP00000502132.1:p.Ser227=
ENST00000675548.1:c.*509T>G	ENSP00000502684.1:n.*509T>G
ENST00000675694.1:c.681T>G	ENSP00000501925.1:p.Ser227=
ENST00000340850.9:c.681T>G	ENSP00000344570.5:p.Ser227=
ENST00000377725.5:c.681T>G	ENSP00000366954.1:p.Ser227=
ENST00000377728.7:c.681T>G	ENSP00000366957.3:p.Ser227=
ENST00000377732.5:c.792T>G	ENSP00000366961.1:p.Ser264=
ENST00000377740.4:c.912T>G	ENSP00000366969.3:p.Ser304=
ENST00000377748.5:c.912T>G	ENSP00000366977.1:p.Ser304=
ENST00000400913.5:c.681T>G	ENSP00000383704.1:p.Ser227=
ENST00000400915.7:c.849T>G	ENSP00000383706.3:p.Ser283=
ENST00000489097.5:n.1157T>G
ENST00000535355.5:c.888T>G	ENSP00000441445.1:p.Ser296=
ENST00000537245.5:c.918T>G	ENSP00000439625.1:p.Ser306=
NM_001042663.1:c.849T>G	NP_001036128.1:p.Ser283=
NM_001042664.1:c.681T>G	NP_001036129.1:p.Ser227=
NM_001042665.1:c.681T>G	NP_001036130.1:p.Ser227=
NM_001265592.1:c.918T>G	NP_001252521.1:p.Ser306=
NM_001265593.1:c.888T>G	NP_001252522.1:p.Ser296=
NM_001265594.1:c.681T>G	NP_001252523.1:p.Ser227=
NM_020631.4:c.681T>G	NP_065682.2:p.Ser227=
NM_198681.3:c.912T>G	NP_941374.2:p.Ser304=
NM_001042663.2:c.849T>G	NP_001036128.1:p.Ser283=
NM_001265594.2:c.681T>G	NP_001252523.1:p.Ser227=
NM_020631.5:c.681T>G	NP_065682.2:p.Ser227=
NM_001042663.3:c.792T>G	NP_001036128.2:p.Ser264=
NM_001265592.2:c.792T>G	NP_001252521.2:p.Ser264=
NM_020631.6:c.681T>G MANE Select	NP_065682.2:p.Ser227=
NM_198681.4:c.681T>G	NP_941374.3:p.Ser227=