Canonical Allele Identifier: CA338115182
Gene: PLEKHG5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.6468128G>A , CM000663.2:g.6468128G>A GRCh38
NC_000001.10:g.6528188G>A , CM000663.1:g.6528188G>A GRCh37
NC_000001.9:g.6450775G>A NCBI36
NG_007978.1:g.56882C>T , LRG_262:g.56882C>T
NG_029910.1:g.3068C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000340850.10:c.2708C>T ENSP00000344570.5:p.Ser903Leu
ENST00000377728.8:c.2708C>T MANE Select ENSP00000366957.3:p.Ser903Leu
ENST00000377740.5:c.2708C>T ENSP00000366969.4:p.Ser903Leu
ENST00000377748.6:c.2882C>T ENSP00000366977.2:p.Ser961Leu
ENST00000400913.6:c.2708C>T ENSP00000383704.1:p.Ser903Leu
ENST00000400915.8:c.2819C>T ENSP00000383706.4:p.Ser940Leu
ENST00000489097.6:n.3184C>T
ENST00000535355.6:c.2915C>T ENSP00000441445.1:p.Ser972Leu
ENST00000537245.6:c.2819C>T ENSP00000439625.2:p.Ser940Leu
ENST00000673471.2:c.3005C>T ENSP00000500749.1:p.Ser1002Leu
ENST00000674790.1:c.*2920C>T ENSP00000502815.1:n.*2920C>T
ENST00000675123.1:c.2250-235C>T ENSP00000502132.1:n.2250-235C>T
ENST00000675548.1:c.*2536C>T ENSP00000502684.1:n.*2536C>T
ENST00000675694.1:c.2708C>T ENSP00000501925.1:p.Ser903Leu
ENST00000675976.1:c.581C>T ENSP00000501611.1:p.Ser194Leu
ENST00000340850.9:c.2708C>T ENSP00000344570.5:p.Ser903Leu
ENST00000377725.5:c.2708C>T ENSP00000366954.1:p.Ser903Leu
ENST00000377728.7:c.2708C>T ENSP00000366957.3:p.Ser903Leu
ENST00000377732.5:c.2819C>T ENSP00000366961.1:p.Ser940Leu
ENST00000377740.4:c.2481-235C>T ENSP00000366969.3:n.2481-235C>T
ENST00000377748.5:c.2939C>T ENSP00000366977.1:p.Ser980Leu
ENST00000400913.5:c.2708C>T ENSP00000383704.1:p.Ser903Leu
ENST00000400915.7:c.2876C>T ENSP00000383706.3:p.Ser959Leu
ENST00000487949.4:n.1910C>T
ENST00000489097.5:n.3184C>T
ENST00000535355.5:c.2915C>T ENSP00000441445.1:p.Ser972Leu
ENST00000537245.5:c.2945C>T ENSP00000439625.1:p.Ser982Leu
NM_001042663.1:c.2876C>T NP_001036128.1:p.Ser959Leu
NM_001042664.1:c.2708C>T NP_001036129.1:p.Ser903Leu
NM_001042665.1:c.2708C>T NP_001036130.1:p.Ser903Leu
NM_001265592.1:c.2945C>T NP_001252521.1:p.Ser982Leu
NM_001265593.1:c.2915C>T NP_001252522.1:p.Ser972Leu
NM_001265594.1:c.2708C>T NP_001252523.1:p.Ser903Leu
NM_020631.4:c.2708C>T NP_065682.2:p.Ser903Leu
NM_198681.3:c.2939C>T NP_941374.2:p.Ser980Leu
NM_001042663.2:c.2876C>T NP_001036128.1:p.Ser959Leu
NM_001265594.2:c.2708C>T NP_001252523.1:p.Ser903Leu
NM_020631.5:c.2708C>T NP_065682.2:p.Ser903Leu
NM_001042663.3:c.2819C>T NP_001036128.2:p.Ser940Leu
NM_001265592.2:c.2819C>T NP_001252521.2:p.Ser940Leu
NM_020631.6:c.2708C>T MANE Select NP_065682.2:p.Ser903Leu
NM_198681.4:c.2708C>T NP_941374.3:p.Ser903Leu