Canonical Allele Identifier: CA338117842

Gene: PLEKHG5

Linked Data

• MyVariant Identifiers: chr1:g.6528620A>G (hg19) ; chr1:g.6468560A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6468560A>G , CM000663.2:g.6468560A>G	GRCh38
NC_000001.10:g.6528620A>G , CM000663.1:g.6528620A>G	GRCh37
NC_000001.9:g.6451207A>G	NCBI36
NG_007978.1:g.56450T>C , LRG_262:g.56450T>C
NG_029910.1:g.2636T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.2276T>C	ENSP00000344570.5:p.Leu759Pro
ENST00000377728.8:c.2276T>C MANE Select	ENSP00000366957.3:p.Leu759Pro
ENST00000377740.5:c.2276T>C	ENSP00000366969.4:p.Leu759Pro
ENST00000377748.6:c.2450T>C	ENSP00000366977.2:p.Leu817Pro
ENST00000400913.6:c.2276T>C	ENSP00000383704.1:p.Leu759Pro
ENST00000400915.8:c.2387T>C	ENSP00000383706.4:p.Leu796Pro
ENST00000489097.6:n.2752T>C
ENST00000535355.6:c.2483T>C	ENSP00000441445.1:p.Leu828Pro
ENST00000537245.6:c.2387T>C	ENSP00000439625.2:p.Leu796Pro
ENST00000673471.2:c.2573T>C	ENSP00000500749.1:p.Leu858Pro
ENST00000674790.1:c.*2488T>C	ENSP00000502815.1:n.*2488T>C
ENST00000675123.1:c.2249+482T>C	ENSP00000502132.1:n.2249+482T>C
ENST00000675548.1:c.*2104T>C	ENSP00000502684.1:n.*2104T>C
ENST00000675694.1:c.2276T>C	ENSP00000501925.1:p.Leu759Pro
ENST00000675976.1:c.149T>C	ENSP00000501611.1:p.Leu50Pro
ENST00000340850.9:c.2276T>C	ENSP00000344570.5:p.Leu759Pro
ENST00000377725.5:c.2276T>C	ENSP00000366954.1:p.Leu759Pro
ENST00000377728.7:c.2276T>C	ENSP00000366957.3:p.Leu759Pro
ENST00000377732.5:c.2387T>C	ENSP00000366961.1:p.Leu796Pro
ENST00000377740.4:c.2480+482T>C	ENSP00000366969.3:n.2480+482T>C
ENST00000377748.5:c.2507T>C	ENSP00000366977.1:p.Leu836Pro
ENST00000400913.5:c.2276T>C	ENSP00000383704.1:p.Leu759Pro
ENST00000400915.7:c.2444T>C	ENSP00000383706.3:p.Leu815Pro
ENST00000487949.4:n.1478T>C
ENST00000489097.5:n.2752T>C
ENST00000535355.5:c.2483T>C	ENSP00000441445.1:p.Leu828Pro
ENST00000537245.5:c.2513T>C	ENSP00000439625.1:p.Leu838Pro
NM_001042663.1:c.2444T>C	NP_001036128.1:p.Leu815Pro
NM_001042664.1:c.2276T>C	NP_001036129.1:p.Leu759Pro
NM_001042665.1:c.2276T>C	NP_001036130.1:p.Leu759Pro
NM_001265592.1:c.2513T>C	NP_001252521.1:p.Leu838Pro
NM_001265593.1:c.2483T>C	NP_001252522.1:p.Leu828Pro
NM_001265594.1:c.2276T>C	NP_001252523.1:p.Leu759Pro
NM_020631.4:c.2276T>C	NP_065682.2:p.Leu759Pro
NM_198681.3:c.2507T>C	NP_941374.2:p.Leu836Pro
NM_001042663.2:c.2444T>C	NP_001036128.1:p.Leu815Pro
NM_001265594.2:c.2276T>C	NP_001252523.1:p.Leu759Pro
NM_020631.5:c.2276T>C	NP_065682.2:p.Leu759Pro
NM_001042663.3:c.2387T>C	NP_001036128.2:p.Leu796Pro
NM_001265592.2:c.2387T>C	NP_001252521.2:p.Leu796Pro
NM_020631.6:c.2276T>C MANE Select	NP_065682.2:p.Leu759Pro
NM_198681.4:c.2276T>C	NP_941374.3:p.Leu759Pro