Canonical Allele Identifier: CA338139297
Gene: PLEKHG5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.6474514T>G , CM000663.2:g.6474514T>G GRCh38
NC_000001.10:g.6534574T>G , CM000663.1:g.6534574T>G GRCh37
NC_000001.9:g.6457161T>G NCBI36
NG_007978.1:g.50496A>C , LRG_262:g.50496A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000340850.10:c.376A>C ENSP00000344570.5:p.Asn126His
ENST00000377728.8:c.376A>C MANE Select ENSP00000366957.3:p.Asn126His
ENST00000377740.5:c.376A>C ENSP00000366969.4:p.Asn126His
ENST00000377748.6:c.550A>C ENSP00000366977.2:p.Asn184His
ENST00000400913.6:c.376A>C ENSP00000383704.1:p.Asn126His
ENST00000400915.8:c.487A>C ENSP00000383706.4:p.Asn163His
ENST00000489097.6:n.852A>C
ENST00000535355.6:c.583A>C ENSP00000441445.1:p.Asn195His
ENST00000537245.6:c.487A>C ENSP00000439625.2:p.Asn163His
ENST00000673471.2:c.673A>C ENSP00000500749.1:p.Asn225His
ENST00000674790.1:c.*588A>C ENSP00000502815.1:n.*588A>C
ENST00000675123.1:c.376A>C ENSP00000502132.1:p.Asn126His
ENST00000675548.1:c.*204A>C ENSP00000502684.1:n.*204A>C
ENST00000675694.1:c.376A>C ENSP00000501925.1:p.Asn126His
ENST00000676255.1:c.338A>C ENSP00000502459.1:n.338A>C
ENST00000340850.9:c.376A>C ENSP00000344570.5:p.Asn126His
ENST00000377725.5:c.376A>C ENSP00000366954.1:p.Asn126His
ENST00000377728.7:c.376A>C ENSP00000366957.3:p.Asn126His
ENST00000377732.5:c.487A>C ENSP00000366961.1:p.Asn163His
ENST00000377740.4:c.607A>C ENSP00000366969.3:p.Asn203His
ENST00000377748.5:c.607A>C ENSP00000366977.1:p.Asn203His
ENST00000400913.5:c.376A>C ENSP00000383704.1:p.Asn126His
ENST00000400915.7:c.544A>C ENSP00000383706.3:p.Asn182His
ENST00000489097.5:n.852A>C
ENST00000535355.5:c.583A>C ENSP00000441445.1:p.Asn195His
ENST00000537245.5:c.613A>C ENSP00000439625.1:p.Asn205His
NM_001042663.1:c.544A>C NP_001036128.1:p.Asn182His
NM_001042664.1:c.376A>C NP_001036129.1:p.Asn126His
NM_001042665.1:c.376A>C NP_001036130.1:p.Asn126His
NM_001265592.1:c.613A>C NP_001252521.1:p.Asn205His
NM_001265593.1:c.583A>C NP_001252522.1:p.Asn195His
NM_001265594.1:c.376A>C NP_001252523.1:p.Asn126His
NM_020631.4:c.376A>C NP_065682.2:p.Asn126His
NM_198681.3:c.607A>C NP_941374.2:p.Asn203His
NM_001042663.2:c.544A>C NP_001036128.1:p.Asn182His
NM_001265594.2:c.376A>C NP_001252523.1:p.Asn126His
NM_020631.5:c.376A>C NP_065682.2:p.Asn126His
NM_001042663.3:c.487A>C NP_001036128.2:p.Asn163His
NM_001265592.2:c.487A>C NP_001252521.2:p.Asn163His
NM_020631.6:c.376A>C MANE Select NP_065682.2:p.Asn126His
NM_198681.4:c.376A>C NP_941374.3:p.Asn126His