Canonical Allele Identifier: CA561766

Gene: PLEKHG5

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6473307C>G , CM000663.2:g.6473307C>G	GRCh38
NC_000001.10:g.6533367C>G , CM000663.1:g.6533367C>G	GRCh37
NC_000001.9:g.6455954C>G	NCBI36
NG_007978.1:g.51703G>C , LRG_262:g.51703G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.739G>C	ENSP00000344570.5:p.Ala247Pro
ENST00000377728.8:c.739G>C MANE Select	ENSP00000366957.3:p.Ala247Pro
ENST00000377740.5:c.739G>C	ENSP00000366969.4:p.Ala247Pro
ENST00000377748.6:c.913G>C	ENSP00000366977.2:p.Ala305Pro
ENST00000400913.6:c.739G>C	ENSP00000383704.1:p.Ala247Pro
ENST00000400915.8:c.850G>C	ENSP00000383706.4:p.Ala284Pro
ENST00000489097.6:n.1215G>C
ENST00000535355.6:c.946G>C	ENSP00000441445.1:p.Ala316Pro
ENST00000537245.6:c.850G>C	ENSP00000439625.2:p.Ala284Pro
ENST00000673471.2:c.1036G>C	ENSP00000500749.1:p.Ala346Pro
ENST00000674790.1:c.*951G>C	ENSP00000502815.1:n.*951G>C
ENST00000675123.1:c.739G>C	ENSP00000502132.1:p.Ala247Pro
ENST00000675548.1:c.*567G>C	ENSP00000502684.1:n.*567G>C
ENST00000675694.1:c.739G>C	ENSP00000501925.1:p.Ala247Pro
ENST00000340850.9:c.739G>C	ENSP00000344570.5:p.Ala247Pro
ENST00000377725.5:c.739G>C	ENSP00000366954.1:p.Ala247Pro
ENST00000377728.7:c.739G>C	ENSP00000366957.3:p.Ala247Pro
ENST00000377732.5:c.850G>C	ENSP00000366961.1:p.Ala284Pro
ENST00000377740.4:c.970G>C	ENSP00000366969.3:p.Ala324Pro
ENST00000377748.5:c.970G>C	ENSP00000366977.1:p.Ala324Pro
ENST00000400913.5:c.739G>C	ENSP00000383704.1:p.Ala247Pro
ENST00000400915.7:c.907G>C	ENSP00000383706.3:p.Ala303Pro
ENST00000489097.5:n.1215G>C
ENST00000535355.5:c.946G>C	ENSP00000441445.1:p.Ala316Pro
ENST00000537245.5:c.976G>C	ENSP00000439625.1:p.Ala326Pro
NM_001042663.1:c.907G>C	NP_001036128.1:p.Ala303Pro
NM_001042664.1:c.739G>C	NP_001036129.1:p.Ala247Pro
NM_001042665.1:c.739G>C	NP_001036130.1:p.Ala247Pro
NM_001265592.1:c.976G>C	NP_001252521.1:p.Ala326Pro
NM_001265593.1:c.946G>C	NP_001252522.1:p.Ala316Pro
NM_001265594.1:c.739G>C	NP_001252523.1:p.Ala247Pro
NM_020631.4:c.739G>C	NP_065682.2:p.Ala247Pro
NM_198681.3:c.970G>C	NP_941374.2:p.Ala324Pro
NM_001042663.2:c.907G>C	NP_001036128.1:p.Ala303Pro
NM_001265594.2:c.739G>C	NP_001252523.1:p.Ala247Pro
NM_020631.5:c.739G>C	NP_065682.2:p.Ala247Pro
NM_001042663.3:c.850G>C	NP_001036128.2:p.Ala284Pro
NM_001265592.2:c.850G>C	NP_001252521.2:p.Ala284Pro
NM_020631.6:c.739G>C MANE Select	NP_065682.2:p.Ala247Pro
NM_198681.4:c.739G>C	NP_941374.3:p.Ala247Pro