Canonical Allele Identifier: CA338138848

Gene: PLEKHG5

Linked Data

• MyVariant Identifiers: chr1:g.6534194A>G (hg19) ; chr1:g.6474134A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6474134A>G , CM000663.2:g.6474134A>G	GRCh38
NC_000001.10:g.6534194A>G , CM000663.1:g.6534194A>G	GRCh37
NC_000001.9:g.6456781A>G	NCBI36
NG_007978.1:g.50876T>C , LRG_262:g.50876T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000340850.10:c.470T>C	ENSP00000344570.5:p.Val157Ala
ENST00000377728.8:c.470T>C MANE Select	ENSP00000366957.3:p.Val157Ala
ENST00000377740.5:c.470T>C	ENSP00000366969.4:p.Val157Ala
ENST00000377748.6:c.644T>C	ENSP00000366977.2:p.Val215Ala
ENST00000400913.6:c.470T>C	ENSP00000383704.1:p.Val157Ala
ENST00000400915.8:c.581T>C	ENSP00000383706.4:p.Val194Ala
ENST00000489097.6:n.946T>C
ENST00000535355.6:c.677T>C	ENSP00000441445.1:p.Val226Ala
ENST00000537245.6:c.581T>C	ENSP00000439625.2:p.Val194Ala
ENST00000673471.2:c.767T>C	ENSP00000500749.1:p.Val256Ala
ENST00000674790.1:c.*682T>C	ENSP00000502815.1:n.*682T>C
ENST00000675123.1:c.470T>C	ENSP00000502132.1:p.Val157Ala
ENST00000675548.1:c.*298T>C	ENSP00000502684.1:n.*298T>C
ENST00000675694.1:c.470T>C	ENSP00000501925.1:p.Val157Ala
ENST00000340850.9:c.470T>C	ENSP00000344570.5:p.Val157Ala
ENST00000377725.5:c.470T>C	ENSP00000366954.1:p.Val157Ala
ENST00000377728.7:c.470T>C	ENSP00000366957.3:p.Val157Ala
ENST00000377732.5:c.581T>C	ENSP00000366961.1:p.Val194Ala
ENST00000377740.4:c.701T>C	ENSP00000366969.3:p.Val234Ala
ENST00000377748.5:c.701T>C	ENSP00000366977.1:p.Val234Ala
ENST00000400913.5:c.470T>C	ENSP00000383704.1:p.Val157Ala
ENST00000400915.7:c.638T>C	ENSP00000383706.3:p.Val213Ala
ENST00000489097.5:n.946T>C
ENST00000535355.5:c.677T>C	ENSP00000441445.1:p.Val226Ala
ENST00000537245.5:c.707T>C	ENSP00000439625.1:p.Val236Ala
NM_001042663.1:c.638T>C	NP_001036128.1:p.Val213Ala
NM_001042664.1:c.470T>C	NP_001036129.1:p.Val157Ala
NM_001042665.1:c.470T>C	NP_001036130.1:p.Val157Ala
NM_001265592.1:c.707T>C	NP_001252521.1:p.Val236Ala
NM_001265593.1:c.677T>C	NP_001252522.1:p.Val226Ala
NM_001265594.1:c.470T>C	NP_001252523.1:p.Val157Ala
NM_020631.4:c.470T>C	NP_065682.2:p.Val157Ala
NM_198681.3:c.701T>C	NP_941374.2:p.Val234Ala
NM_001042663.2:c.638T>C	NP_001036128.1:p.Val213Ala
NM_001265594.2:c.470T>C	NP_001252523.1:p.Val157Ala
NM_020631.5:c.470T>C	NP_065682.2:p.Val157Ala
NM_001042663.3:c.581T>C	NP_001036128.2:p.Val194Ala
NM_001265592.2:c.581T>C	NP_001252521.2:p.Val194Ala
NM_020631.6:c.470T>C MANE Select	NP_065682.2:p.Val157Ala
NM_198681.4:c.470T>C	NP_941374.3:p.Val157Ala