Canonical Allele Identifier: CA416022503

Gene: PLEKHG5

Linked Data

• MyVariant Identifiers: chr1:g.6529245C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6469185C>T , CM000663.2:g.6469185C>T	GRCh38
NC_000001.10:g.6529245C>T , CM000663.1:g.6529245C>T	GRCh37
NC_000001.9:g.6451832C>T	NCBI36
NG_007978.1:g.55825G>A , LRG_262:g.55825G>A
NG_029910.1:g.2011G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.2106G>A	ENSP00000344570.5:p.Gln702=
ENST00000377728.8:c.2106G>A MANE Select	ENSP00000366957.3:p.Gln702=
ENST00000377740.5:c.2106G>A	ENSP00000366969.4:p.Gln702=
ENST00000377748.6:c.2280G>A	ENSP00000366977.2:p.Gln760=
ENST00000400913.6:c.2106G>A	ENSP00000383704.1:p.Gln702=
ENST00000400915.8:c.2217G>A	ENSP00000383706.4:p.Gln739=
ENST00000489097.6:n.2582G>A
ENST00000535355.6:c.2313G>A	ENSP00000441445.1:p.Gln771=
ENST00000537245.6:c.2217G>A	ENSP00000439625.2:p.Gln739=
ENST00000673471.2:c.2403G>A	ENSP00000500749.1:p.Gln801=
ENST00000674790.1:c.*2318G>A	ENSP00000502815.1:n.*2318G>A
ENST00000675123.1:c.2106G>A	ENSP00000502132.1:p.Gln702=
ENST00000675139.1:n.177G>A
ENST00000675548.1:c.*1934G>A	ENSP00000502684.1:n.*1934G>A
ENST00000675694.1:c.2106G>A	ENSP00000501925.1:p.Gln702=
ENST00000340850.9:c.2106G>A	ENSP00000344570.5:p.Gln702=
ENST00000377725.5:c.2106G>A	ENSP00000366954.1:p.Gln702=
ENST00000377728.7:c.2106G>A	ENSP00000366957.3:p.Gln702=
ENST00000377732.5:c.2217G>A	ENSP00000366961.1:p.Gln739=
ENST00000377740.4:c.2337G>A	ENSP00000366969.3:p.Gln779=
ENST00000377748.5:c.2337G>A	ENSP00000366977.1:p.Gln779=
ENST00000400913.5:c.2106G>A	ENSP00000383704.1:p.Gln702=
ENST00000400915.7:c.2274G>A	ENSP00000383706.3:p.Gln758=
ENST00000487949.4:n.1308G>A
ENST00000489097.5:n.2582G>A
ENST00000535355.5:c.2313G>A	ENSP00000441445.1:p.Gln771=
ENST00000537245.5:c.2343G>A	ENSP00000439625.1:p.Gln781=
NM_001042663.1:c.2274G>A	NP_001036128.1:p.Gln758=
NM_001042664.1:c.2106G>A	NP_001036129.1:p.Gln702=
NM_001042665.1:c.2106G>A	NP_001036130.1:p.Gln702=
NM_001265592.1:c.2343G>A	NP_001252521.1:p.Gln781=
NM_001265593.1:c.2313G>A	NP_001252522.1:p.Gln771=
NM_001265594.1:c.2106G>A	NP_001252523.1:p.Gln702=
NM_020631.4:c.2106G>A	NP_065682.2:p.Gln702=
NM_198681.3:c.2337G>A	NP_941374.2:p.Gln779=
NM_001042663.2:c.2274G>A	NP_001036128.1:p.Gln758=
NM_001265594.2:c.2106G>A	NP_001252523.1:p.Gln702=
NM_020631.5:c.2106G>A	NP_065682.2:p.Gln702=
NM_001042663.3:c.2217G>A	NP_001036128.2:p.Gln739=
NM_001265592.2:c.2217G>A	NP_001252521.2:p.Gln739=
NM_020631.6:c.2106G>A MANE Select	NP_065682.2:p.Gln702=
NM_198681.4:c.2106G>A	NP_941374.3:p.Gln702=