Canonical Allele Identifier: CA2839601364
Gene: PLEKHG5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.6477685A>C , CM000663.2:g.6477685A>C GRCh38
NC_000001.10:g.6537745A>C , CM000663.1:g.6537745A>C GRCh37
NC_000001.9:g.6460332A>C NCBI36
NG_007978.1:g.47325T>G , LRG_262:g.47325T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000340850.10:c.-87-27T>G ENSP00000344570.5:n.-87-27T>G
ENST00000377728.8:c.-87-27T>G MANE Select ENSP00000366957.3:n.-87-27T>G
ENST00000377740.5:c.-87-27T>G ENSP00000366969.4:n.-87-27T>G
ENST00000377748.6:c.25-27T>G ENSP00000366977.2:n.25-27T>G
ENST00000400913.6:c.-87-27T>G ENSP00000383704.1:n.-87-27T>G
ENST00000400915.8:c.25-27T>G ENSP00000383706.4:n.25-27T>G
ENST00000535355.6:c.121-27T>G ENSP00000441445.1:n.121-27T>G
ENST00000537245.6:c.25-27T>G ENSP00000439625.2:n.25-27T>G
ENST00000673471.2:c.211-27T>G ENSP00000500749.1:n.211-27T>G
ENST00000674790.1:c.*126-27T>G ENSP00000502815.1:n.*126-27T>G
ENST00000674803.1:n.144-27T>G
ENST00000675093.1:c.-87-27T>G ENSP00000502687.1:n.-87-27T>G
ENST00000675548.1:c.99-27T>G ENSP00000502684.1:n.99-27T>G
ENST00000675655.1:n.120-27T>G
ENST00000675694.1:c.-87-27T>G ENSP00000501925.1:n.-87-27T>G
ENST00000676287.1:c.-87-27T>G ENSP00000502810.1:n.-87-27T>G
ENST00000676362.1:n.137-27T>G
ENST00000340850.9:c.-87-27T>G ENSP00000344570.5:n.-87-27T>G
ENST00000377725.5:c.-87-27T>G ENSP00000366954.1:n.-87-27T>G
ENST00000377728.7:c.-87-27T>G ENSP00000366957.3:n.-87-27T>G
ENST00000377732.5:c.25-27T>G ENSP00000366961.1:n.25-27T>G
ENST00000377740.4:c.145-27T>G ENSP00000366969.3:n.145-27T>G
ENST00000377748.5:c.145-27T>G ENSP00000366977.1:n.145-27T>G
ENST00000400913.5:c.-87-27T>G ENSP00000383704.1:n.-87-27T>G
ENST00000400915.7:c.82-27T>G ENSP00000383706.3:n.82-27T>G
ENST00000535355.5:c.121-27T>G ENSP00000441445.1:n.121-27T>G
ENST00000537245.5:c.151-27T>G ENSP00000439625.1:n.151-27T>G
NM_001042663.1:c.82-27T>G NP_001036128.1:n.82-27T>G
NM_001042664.1:c.-87-27T>G NP_001036129.1:n.-87-27T>G
NM_001042665.1:c.-87-27T>G NP_001036130.1:n.-87-27T>G
NM_001265592.1:c.151-27T>G NP_001252521.1:n.151-27T>G
NM_001265593.1:c.121-27T>G NP_001252522.1:n.121-27T>G
NM_001265594.1:c.-87-27T>G NP_001252523.1:n.-87-27T>G
NM_020631.4:c.-87-27T>G NP_065682.2:n.-87-27T>G
NM_198681.3:c.145-27T>G NP_941374.2:n.145-27T>G
NM_001042663.2:c.82-27T>G NP_001036128.1:n.82-27T>G
NM_001265594.2:c.-87-27T>G NP_001252523.1:n.-87-27T>G
NM_020631.5:c.-87-27T>G NP_065682.2:n.-87-27T>G
NM_001042663.3:c.25-27T>G NP_001036128.2:n.25-27T>G
NM_001265592.2:c.25-27T>G NP_001252521.2:n.25-27T>G
NM_020631.6:c.-87-27T>G MANE Select NP_065682.2:n.-87-27T>G
NM_198681.4:c.-87-27T>G NP_941374.3:n.-87-27T>G