Canonical Allele Identifier: CA338116106

Gene: PLEKHG5

Linked Data

• gnomAD v4: 1-6468287-G-T
• MyVariant Identifiers: chr1:g.6528347G>T (hg19) ; chr1:g.6468287G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6468287G>T , CM000663.2:g.6468287G>T	GRCh38
NC_000001.10:g.6528347G>T , CM000663.1:g.6528347G>T	GRCh37
NC_000001.9:g.6450934G>T	NCBI36
NG_007978.1:g.56723C>A , LRG_262:g.56723C>A
NG_029910.1:g.2909C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000340850.10:c.2549C>A	ENSP00000344570.5:p.Pro850His
ENST00000377728.8:c.2549C>A MANE Select	ENSP00000366957.3:p.Pro850His
ENST00000377740.5:c.2549C>A	ENSP00000366969.4:p.Pro850His
ENST00000377748.6:c.2723C>A	ENSP00000366977.2:p.Pro908His
ENST00000400913.6:c.2549C>A	ENSP00000383704.1:p.Pro850His
ENST00000400915.8:c.2660C>A	ENSP00000383706.4:p.Pro887His
ENST00000489097.6:n.3025C>A
ENST00000535355.6:c.2756C>A	ENSP00000441445.1:p.Pro919His
ENST00000537245.6:c.2660C>A	ENSP00000439625.2:p.Pro887His
ENST00000673471.2:c.2846C>A	ENSP00000500749.1:p.Pro949His
ENST00000674790.1:c.*2761C>A	ENSP00000502815.1:n.*2761C>A
ENST00000675123.1:c.2250-394C>A	ENSP00000502132.1:n.2250-394C>A
ENST00000675548.1:c.*2377C>A	ENSP00000502684.1:n.*2377C>A
ENST00000675694.1:c.2549C>A	ENSP00000501925.1:p.Pro850His
ENST00000675976.1:c.422C>A	ENSP00000501611.1:p.Pro141His
ENST00000340850.9:c.2549C>A	ENSP00000344570.5:p.Pro850His
ENST00000377725.5:c.2549C>A	ENSP00000366954.1:p.Pro850His
ENST00000377728.7:c.2549C>A	ENSP00000366957.3:p.Pro850His
ENST00000377732.5:c.2660C>A	ENSP00000366961.1:p.Pro887His
ENST00000377740.4:c.2481-394C>A	ENSP00000366969.3:n.2481-394C>A
ENST00000377748.5:c.2780C>A	ENSP00000366977.1:p.Pro927His
ENST00000400913.5:c.2549C>A	ENSP00000383704.1:p.Pro850His
ENST00000400915.7:c.2717C>A	ENSP00000383706.3:p.Pro906His
ENST00000487949.4:n.1751C>A
ENST00000489097.5:n.3025C>A
ENST00000535355.5:c.2756C>A	ENSP00000441445.1:p.Pro919His
ENST00000537245.5:c.2786C>A	ENSP00000439625.1:p.Pro929His
NM_001042663.1:c.2717C>A	NP_001036128.1:p.Pro906His
NM_001042664.1:c.2549C>A	NP_001036129.1:p.Pro850His
NM_001042665.1:c.2549C>A	NP_001036130.1:p.Pro850His
NM_001265592.1:c.2786C>A	NP_001252521.1:p.Pro929His
NM_001265593.1:c.2756C>A	NP_001252522.1:p.Pro919His
NM_001265594.1:c.2549C>A	NP_001252523.1:p.Pro850His
NM_020631.4:c.2549C>A	NP_065682.2:p.Pro850His
NM_198681.3:c.2780C>A	NP_941374.2:p.Pro927His
NM_001042663.2:c.2717C>A	NP_001036128.1:p.Pro906His
NM_001265594.2:c.2549C>A	NP_001252523.1:p.Pro850His
NM_020631.5:c.2549C>A	NP_065682.2:p.Pro850His
NM_001042663.3:c.2660C>A	NP_001036128.2:p.Pro887His
NM_001265592.2:c.2660C>A	NP_001252521.2:p.Pro887His
NM_020631.6:c.2549C>A MANE Select	NP_065682.2:p.Pro850His
NM_198681.4:c.2549C>A	NP_941374.3:p.Pro850His