Canonical Allele Identifier: CA338141899

Gene: PLEKHG5

Linked Data

• MyVariant Identifiers: chr1:g.6537606A>T (hg19) ; chr1:g.6477546A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6477546A>T , CM000663.2:g.6477546A>T	GRCh38
NC_000001.10:g.6537606A>T , CM000663.1:g.6537606A>T	GRCh37
NC_000001.9:g.6460193A>T	NCBI36
NG_007978.1:g.47464T>A , LRG_262:g.47464T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340850.10:c.26T>A	ENSP00000344570.5:p.Phe9Tyr
ENST00000377728.8:c.26T>A MANE Select	ENSP00000366957.3:p.Phe9Tyr
ENST00000377740.5:c.26T>A	ENSP00000366969.4:p.Phe9Tyr
ENST00000377748.6:c.137T>A	ENSP00000366977.2:p.Phe46Tyr
ENST00000400913.6:c.26T>A	ENSP00000383704.1:p.Phe9Tyr
ENST00000400915.8:c.137T>A	ENSP00000383706.4:p.Phe46Tyr
ENST00000489097.6:n.43T>A
ENST00000535355.6:c.233T>A	ENSP00000441445.1:p.Phe78Tyr
ENST00000537245.6:c.137T>A	ENSP00000439625.2:p.Phe46Tyr
ENST00000673471.2:c.323T>A	ENSP00000500749.1:p.Phe108Tyr
ENST00000674790.1:c.*238T>A	ENSP00000502815.1:n.*238T>A
ENST00000674803.1:n.256T>A
ENST00000675093.1:c.26T>A	ENSP00000502687.1:p.Phe9Tyr
ENST00000675123.1:c.26T>A	ENSP00000502132.1:p.Phe9Tyr
ENST00000675548.1:c.211T>A	ENSP00000502684.1:p.Ser71Thr
ENST00000675655.1:n.232T>A
ENST00000675694.1:c.26T>A	ENSP00000501925.1:p.Phe9Tyr
ENST00000676287.1:c.26T>A	ENSP00000502810.1:p.Phe9Tyr
ENST00000676362.1:n.249T>A
ENST00000340850.9:c.26T>A	ENSP00000344570.5:p.Phe9Tyr
ENST00000377725.5:c.26T>A	ENSP00000366954.1:p.Phe9Tyr
ENST00000377728.7:c.26T>A	ENSP00000366957.3:p.Phe9Tyr
ENST00000377732.5:c.137T>A	ENSP00000366961.1:p.Phe46Tyr
ENST00000377740.4:c.257T>A	ENSP00000366969.3:p.Phe86Tyr
ENST00000377748.5:c.257T>A	ENSP00000366977.1:p.Phe86Tyr
ENST00000400913.5:c.26T>A	ENSP00000383704.1:p.Phe9Tyr
ENST00000400915.7:c.194T>A	ENSP00000383706.3:p.Phe65Tyr
ENST00000489097.5:n.43T>A
ENST00000535355.5:c.233T>A	ENSP00000441445.1:p.Phe78Tyr
ENST00000537245.5:c.263T>A	ENSP00000439625.1:p.Phe88Tyr
NM_001042663.1:c.194T>A	NP_001036128.1:p.Phe65Tyr
NM_001042664.1:c.26T>A	NP_001036129.1:p.Phe9Tyr
NM_001042665.1:c.26T>A	NP_001036130.1:p.Phe9Tyr
NM_001265592.1:c.263T>A	NP_001252521.1:p.Phe88Tyr
NM_001265593.1:c.233T>A	NP_001252522.1:p.Phe78Tyr
NM_001265594.1:c.26T>A	NP_001252523.1:p.Phe9Tyr
NM_020631.4:c.26T>A	NP_065682.2:p.Phe9Tyr
NM_198681.3:c.257T>A	NP_941374.2:p.Phe86Tyr
NM_001042663.2:c.194T>A	NP_001036128.1:p.Phe65Tyr
NM_001265594.2:c.26T>A	NP_001252523.1:p.Phe9Tyr
NM_020631.5:c.26T>A	NP_065682.2:p.Phe9Tyr
NM_001042663.3:c.137T>A	NP_001036128.2:p.Phe46Tyr
NM_001265592.2:c.137T>A	NP_001252521.2:p.Phe46Tyr
NM_020631.6:c.26T>A MANE Select	NP_065682.2:p.Phe9Tyr
NM_198681.4:c.26T>A	NP_941374.3:p.Phe9Tyr