Canonical Allele Identifier: CA1151507688
Gene: PLEKHG5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.6474809C= , CM000663.2:g.6474809C= GRCh38
NC_000001.10:g.6534869C= , CM000663.1:g.6534869C= GRCh37
NC_000001.9:g.6457456C= NCBI36
NG_007978.1:g.50201G= , LRG_262:g.50201G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000340850.10:c.303-222G= ENSP00000344570.5:n.303-222G=
ENST00000377728.8:c.303-222G= MANE Select ENSP00000366957.3:n.303-222G=
ENST00000377740.5:c.303-222G= ENSP00000366969.4:n.303-222G=
ENST00000377748.6:c.477-222G= ENSP00000366977.2:n.477-222G=
ENST00000400913.6:c.303-222G= ENSP00000383704.1:n.303-222G=
ENST00000400915.8:c.414-222G= ENSP00000383706.4:n.414-222G=
ENST00000489097.6:n.557G=
ENST00000535355.6:c.510-222G= ENSP00000441445.1:n.510-222G=
ENST00000537245.6:c.414-222G= ENSP00000439625.2:n.414-222G=
ENST00000673471.2:c.600-222G= ENSP00000500749.1:n.600-222G=
ENST00000674790.1:c.*515-222G= ENSP00000502815.1:n.*515-222G=
ENST00000675093.1:c.303-222G= ENSP00000502687.1:n.303-222G=
ENST00000675123.1:c.303-222G= ENSP00000502132.1:n.303-222G=
ENST00000675548.1:c.*131-222G= ENSP00000502684.1:n.*131-222G=
ENST00000675694.1:c.303-222G= ENSP00000501925.1:n.303-222G=
ENST00000676255.1:c.152G= ENSP00000502459.1:p.Gly51=
ENST00000676287.1:c.303-222G= ENSP00000502810.1:n.303-222G=
ENST00000340850.9:c.303-222G= ENSP00000344570.5:n.303-222G=
ENST00000377725.5:c.303-222G= ENSP00000366954.1:n.303-222G=
ENST00000377728.7:c.303-222G= ENSP00000366957.3:n.303-222G=
ENST00000377732.5:c.414-222G= ENSP00000366961.1:n.414-222G=
ENST00000377740.4:c.534-222G= ENSP00000366969.3:n.534-222G=
ENST00000377748.5:c.534-222G= ENSP00000366977.1:n.534-222G=
ENST00000400913.5:c.303-222G= ENSP00000383704.1:n.303-222G=
ENST00000400915.7:c.471-222G= ENSP00000383706.3:n.471-222G=
ENST00000489097.5:n.557G=
ENST00000535355.5:c.510-222G= ENSP00000441445.1:n.510-222G=
ENST00000537245.5:c.540-222G= ENSP00000439625.1:n.540-222G=
NM_001042663.1:c.471-222G= NP_001036128.1:n.471-222G=
NM_001042664.1:c.303-222G= NP_001036129.1:n.303-222G=
NM_001042665.1:c.303-222G= NP_001036130.1:n.303-222G=
NM_001265592.1:c.540-222G= NP_001252521.1:n.540-222G=
NM_001265593.1:c.510-222G= NP_001252522.1:n.510-222G=
NM_001265594.1:c.303-222G= NP_001252523.1:n.303-222G=
NM_020631.4:c.303-222G= NP_065682.2:n.303-222G=
NM_198681.3:c.534-222G= NP_941374.2:n.534-222G=
NM_001042663.2:c.471-222G= NP_001036128.1:n.471-222G=
NM_001265594.2:c.303-222G= NP_001252523.1:n.303-222G=
NM_020631.5:c.303-222G= NP_065682.2:n.303-222G=
NM_001042663.3:c.414-222G= NP_001036128.2:n.414-222G=
NM_001265592.2:c.414-222G= NP_001252521.2:n.414-222G=
NM_020631.6:c.303-222G= MANE Select NP_065682.2:n.303-222G=
NM_198681.4:c.303-222G= NP_941374.3:n.303-222G=