Canonical Allele Identifier: CA1151525148
Gene: PLEKHG5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.6470727A= , CM000663.2:g.6470727A= GRCh38
NC_000001.10:g.6530787A= , CM000663.1:g.6530787A= GRCh37
NC_000001.9:g.6453374A= NCBI36
NG_007978.1:g.54283T= , LRG_262:g.54283T=
NG_029910.1:g.469T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000340850.10:c.1542+8T= ENSP00000344570.5:n.1542+8T=
ENST00000377728.8:c.1542+8T= MANE Select ENSP00000366957.3:n.1542+8T=
ENST00000377740.5:c.1542+8T= ENSP00000366969.4:n.1542+8T=
ENST00000377748.6:c.1716+8T= ENSP00000366977.2:n.1716+8T=
ENST00000400913.6:c.1542+8T= ENSP00000383704.1:n.1542+8T=
ENST00000400915.8:c.1653+8T= ENSP00000383706.4:n.1653+8T=
ENST00000489097.6:n.2018+8T=
ENST00000535355.6:c.1749+8T= ENSP00000441445.1:n.1749+8T=
ENST00000537245.6:c.1653+8T= ENSP00000439625.2:n.1653+8T=
ENST00000673471.2:c.1839+8T= ENSP00000500749.1:n.1839+8T=
ENST00000674685.1:n.575+8T=
ENST00000674790.1:c.*1754+8T= ENSP00000502815.1:n.*1754+8T=
ENST00000674943.1:n.204+8T=
ENST00000675123.1:c.1542+8T= ENSP00000502132.1:n.1542+8T=
ENST00000675548.1:c.*1370+8T= ENSP00000502684.1:n.*1370+8T=
ENST00000675694.1:c.1542+8T= ENSP00000501925.1:n.1542+8T=
ENST00000676401.1:n.6T=
ENST00000340850.9:c.1542+8T= ENSP00000344570.5:n.1542+8T=
ENST00000377725.5:c.1542+8T= ENSP00000366954.1:n.1542+8T=
ENST00000377728.7:c.1542+8T= ENSP00000366957.3:n.1542+8T=
ENST00000377732.5:c.1653+8T= ENSP00000366961.1:n.1653+8T=
ENST00000377740.4:c.1773+8T= ENSP00000366969.3:n.1773+8T=
ENST00000377748.5:c.1773+8T= ENSP00000366977.1:n.1773+8T=
ENST00000400913.5:c.1542+8T= ENSP00000383704.1:n.1542+8T=
ENST00000400915.7:c.1710+8T= ENSP00000383706.3:n.1710+8T=
ENST00000487949.4:n.744+8T=
ENST00000489097.5:n.2018+8T=
ENST00000535355.5:c.1749+8T= ENSP00000441445.1:n.1749+8T=
ENST00000537245.5:c.1779+8T= ENSP00000439625.1:n.1779+8T=
NM_001042663.1:c.1710+8T= NP_001036128.1:n.1710+8T=
NM_001042664.1:c.1542+8T= NP_001036129.1:n.1542+8T=
NM_001042665.1:c.1542+8T= NP_001036130.1:n.1542+8T=
NM_001265592.1:c.1779+8T= NP_001252521.1:n.1779+8T=
NM_001265593.1:c.1749+8T= NP_001252522.1:n.1749+8T=
NM_001265594.1:c.1542+8T= NP_001252523.1:n.1542+8T=
NM_020631.4:c.1542+8T= NP_065682.2:n.1542+8T=
NM_198681.3:c.1773+8T= NP_941374.2:n.1773+8T=
NM_001042663.2:c.1710+8T= NP_001036128.1:n.1710+8T=
NM_001265594.2:c.1542+8T= NP_001252523.1:n.1542+8T=
NM_020631.5:c.1542+8T= NP_065682.2:n.1542+8T=
NM_001042663.3:c.1653+8T= NP_001036128.2:n.1653+8T=
NM_001265592.2:c.1653+8T= NP_001252521.2:n.1653+8T=
NM_020631.6:c.1542+8T= MANE Select NP_065682.2:n.1542+8T=
NM_198681.4:c.1542+8T= NP_941374.3:n.1542+8T=