Canonical Allele Identifier: CA338138745
Gene: PLEKHG5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.6474110T>G , CM000663.2:g.6474110T>G GRCh38
NC_000001.10:g.6534170T>G , CM000663.1:g.6534170T>G GRCh37
NC_000001.9:g.6456757T>G NCBI36
NG_007978.1:g.50900A>C , LRG_262:g.50900A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000340850.10:c.494A>C ENSP00000344570.5:p.Lys165Thr
ENST00000377728.8:c.494A>C MANE Select ENSP00000366957.3:p.Lys165Thr
ENST00000377740.5:c.494A>C ENSP00000366969.4:p.Lys165Thr
ENST00000377748.6:c.668A>C ENSP00000366977.2:p.Lys223Thr
ENST00000400913.6:c.494A>C ENSP00000383704.1:p.Lys165Thr
ENST00000400915.8:c.605A>C ENSP00000383706.4:p.Lys202Thr
ENST00000489097.6:n.970A>C
ENST00000535355.6:c.701A>C ENSP00000441445.1:p.Lys234Thr
ENST00000537245.6:c.605A>C ENSP00000439625.2:p.Lys202Thr
ENST00000673471.2:c.791A>C ENSP00000500749.1:p.Lys264Thr
ENST00000674790.1:c.*706A>C ENSP00000502815.1:n.*706A>C
ENST00000675123.1:c.494A>C ENSP00000502132.1:p.Lys165Thr
ENST00000675548.1:c.*322A>C ENSP00000502684.1:n.*322A>C
ENST00000675694.1:c.494A>C ENSP00000501925.1:p.Lys165Thr
ENST00000340850.9:c.494A>C ENSP00000344570.5:p.Lys165Thr
ENST00000377725.5:c.494A>C ENSP00000366954.1:p.Lys165Thr
ENST00000377728.7:c.494A>C ENSP00000366957.3:p.Lys165Thr
ENST00000377732.5:c.605A>C ENSP00000366961.1:p.Lys202Thr
ENST00000377740.4:c.725A>C ENSP00000366969.3:p.Lys242Thr
ENST00000377748.5:c.725A>C ENSP00000366977.1:p.Lys242Thr
ENST00000400913.5:c.494A>C ENSP00000383704.1:p.Lys165Thr
ENST00000400915.7:c.662A>C ENSP00000383706.3:p.Lys221Thr
ENST00000489097.5:n.970A>C
ENST00000535355.5:c.701A>C ENSP00000441445.1:p.Lys234Thr
ENST00000537245.5:c.731A>C ENSP00000439625.1:p.Lys244Thr
NM_001042663.1:c.662A>C NP_001036128.1:p.Lys221Thr
NM_001042664.1:c.494A>C NP_001036129.1:p.Lys165Thr
NM_001042665.1:c.494A>C NP_001036130.1:p.Lys165Thr
NM_001265592.1:c.731A>C NP_001252521.1:p.Lys244Thr
NM_001265593.1:c.701A>C NP_001252522.1:p.Lys234Thr
NM_001265594.1:c.494A>C NP_001252523.1:p.Lys165Thr
NM_020631.4:c.494A>C NP_065682.2:p.Lys165Thr
NM_198681.3:c.725A>C NP_941374.2:p.Lys242Thr
NM_001042663.2:c.662A>C NP_001036128.1:p.Lys221Thr
NM_001265594.2:c.494A>C NP_001252523.1:p.Lys165Thr
NM_020631.5:c.494A>C NP_065682.2:p.Lys165Thr
NM_001042663.3:c.605A>C NP_001036128.2:p.Lys202Thr
NM_001265592.2:c.605A>C NP_001252521.2:p.Lys202Thr
NM_020631.6:c.494A>C MANE Select NP_065682.2:p.Lys165Thr
NM_198681.4:c.494A>C NP_941374.3:p.Lys165Thr