Canonical Allele Identifier: CA1151520715
Gene: PLEKHG5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.6469187G= , CM000663.2:g.6469187G= GRCh38
NC_000001.10:g.6529247G= , CM000663.1:g.6529247G= GRCh37
NC_000001.9:g.6451834G= NCBI36
NG_007978.1:g.55823C= , LRG_262:g.55823C=
NG_029910.1:g.2009C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000340850.10:c.2104C= ENSP00000344570.5:p.Gln702=
ENST00000377728.8:c.2104C= MANE Select ENSP00000366957.3:p.Gln702=
ENST00000377740.5:c.2104C= ENSP00000366969.4:p.Gln702=
ENST00000377748.6:c.2278C= ENSP00000366977.2:p.Gln760=
ENST00000400913.6:c.2104C= ENSP00000383704.1:p.Gln702=
ENST00000400915.8:c.2215C= ENSP00000383706.4:p.Gln739=
ENST00000489097.6:n.2580C=
ENST00000535355.6:c.2311C= ENSP00000441445.1:p.Gln771=
ENST00000537245.6:c.2215C= ENSP00000439625.2:p.Gln739=
ENST00000673471.2:c.2401C= ENSP00000500749.1:p.Gln801=
ENST00000674790.1:c.*2316C= ENSP00000502815.1:n.*2316C=
ENST00000675123.1:c.2104C= ENSP00000502132.1:p.Gln702=
ENST00000675139.1:n.175C=
ENST00000675548.1:c.*1932C= ENSP00000502684.1:n.*1932C=
ENST00000675694.1:c.2104C= ENSP00000501925.1:p.Gln702=
ENST00000340850.9:c.2104C= ENSP00000344570.5:p.Gln702=
ENST00000377725.5:c.2104C= ENSP00000366954.1:p.Gln702=
ENST00000377728.7:c.2104C= ENSP00000366957.3:p.Gln702=
ENST00000377732.5:c.2215C= ENSP00000366961.1:p.Gln739=
ENST00000377740.4:c.2335C= ENSP00000366969.3:p.Gln779=
ENST00000377748.5:c.2335C= ENSP00000366977.1:p.Gln779=
ENST00000400913.5:c.2104C= ENSP00000383704.1:p.Gln702=
ENST00000400915.7:c.2272C= ENSP00000383706.3:p.Gln758=
ENST00000487949.4:n.1306C=
ENST00000489097.5:n.2580C=
ENST00000535355.5:c.2311C= ENSP00000441445.1:p.Gln771=
ENST00000537245.5:c.2341C= ENSP00000439625.1:p.Gln781=
NM_001042663.1:c.2272C= NP_001036128.1:p.Gln758=
NM_001042664.1:c.2104C= NP_001036129.1:p.Gln702=
NM_001042665.1:c.2104C= NP_001036130.1:p.Gln702=
NM_001265592.1:c.2341C= NP_001252521.1:p.Gln781=
NM_001265593.1:c.2311C= NP_001252522.1:p.Gln771=
NM_001265594.1:c.2104C= NP_001252523.1:p.Gln702=
NM_020631.4:c.2104C= NP_065682.2:p.Gln702=
NM_198681.3:c.2335C= NP_941374.2:p.Gln779=
NM_001042663.2:c.2272C= NP_001036128.1:p.Gln758=
NM_001265594.2:c.2104C= NP_001252523.1:p.Gln702=
NM_020631.5:c.2104C= NP_065682.2:p.Gln702=
NM_001042663.3:c.2215C= NP_001036128.2:p.Gln739=
NM_001265592.2:c.2215C= NP_001252521.2:p.Gln739=
NM_020631.6:c.2104C= MANE Select NP_065682.2:p.Gln702=
NM_198681.4:c.2104C= NP_941374.3:p.Gln702=