Canonical Allele Identifier: CA6506851
Gene: FGD4 HGNC NCBI

Linked Data

dbSNP Id: rs748420696

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32611190C>A , CM000674.2:g.32611190C>A GRCh38
NC_000012.11:g.32764124C>A , CM000674.1:g.32764124C>A GRCh37
NC_000012.10:g.32655391C>A NCBI36
NG_008626.2:g.216662C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000427716.7:c.1245C>A ENSP00000394487.2:p.Asp415Glu
ENST00000531134.7:c.1500C>A ENSP00000431323.1:p.Asp500Glu
ENST00000583694.2:c.1245C>A ENSP00000462623.2:p.Asp415Glu
ENST00000682739.1:c.966C>A ENSP00000507616.1:p.Asp322Glu
ENST00000683182.1:c.57C>A ENSP00000507831.1:p.Asp19Glu
ENST00000683515.1:n.752C>A
ENST00000525053.6:c.1245C>A ENSP00000433666.2:p.Asp415Glu
ENST00000531134.6:c.1500C>A ENSP00000431323.1:p.Asp500Glu
ENST00000534526.7:c.1656C>A MANE Select ENSP00000449273.1:p.Asp552Glu
ENST00000395740.5:c.*637C>A ENSP00000379089.1:n.*637C>A
ENST00000427716.6:c.1245C>A ENSP00000394487.2:p.Asp415Glu
ENST00000493087.5:c.*656C>A ENSP00000437109.1:n.*656C>A
ENST00000494977.1:c.834C>A
ENST00000525053.5:c.1581C>A ENSP00000433666.1:p.Asp527Glu
ENST00000531134.5:c.1500C>A ENSP00000431323.1:p.Asp500Glu
ENST00000534526.6:c.1656C>A ENSP00000449273.1:p.Asp552Glu
ENST00000546442.5:c.966C>A ENSP00000446695.1:p.Asp322Glu
ENST00000551984.5:c.*614C>A ENSP00000449614.1:n.*614C>A
NM_001304480.1:c.1581C>A NP_001291409.1:p.Asp527Glu
NM_001304481.1:c.1500C>A NP_001291410.1:p.Asp500Glu
NM_001304483.1:c.501C>A NP_001291412.1:p.Asp167Glu
NM_001304484.1:c.213C>A NP_001291413.1:p.Asp71Glu
NM_139241.3:c.1245C>A NP_640334.2:p.Asp415Glu
XM_005253304.3:c.1737C>A XP_005253361.1:p.Asp579Glu
XM_005253307.2:c.966C>A XP_005253364.1:p.Asp322Glu
XM_005253308.3:c.966C>A XP_005253365.1:p.Asp322Glu
XM_005253309.1:c.966C>A XP_005253366.1:p.Asp322Glu
XM_005253310.3:c.501C>A XP_005253367.1:p.Asp167Glu
XM_011520554.1:c.1539C>A XP_011518856.1:p.Asp513Glu
XM_011520555.1:c.1245C>A XP_011518857.1:p.Asp415Glu
XM_011520556.1:c.1245C>A XP_011518858.1:p.Asp415Glu
XM_011520557.1:c.693C>A XP_011518859.1:p.Asp231Glu
XM_011520558.1:c.648C>A XP_011518860.1:p.Asp216Glu
XM_011520559.1:c.480C>A XP_011518861.1:p.Asp160Glu
NM_001330373.1:c.966C>A NP_001317302.1:p.Asp322Glu
NM_001330374.1:c.966C>A NP_001317303.1:p.Asp322Glu
XM_005253304.4:c.1737C>A XP_005253361.1:p.Asp579Glu
XM_005253308.5:c.966C>A XP_005253365.1:p.Asp322Glu
XM_005253310.4:c.501C>A XP_005253367.1:p.Asp167Glu
XM_011520558.2:c.648C>A XP_011518860.1:p.Asp216Glu
XM_011520559.3:c.480C>A XP_011518861.1:p.Asp160Glu
XM_017018803.1:c.1737C>A XP_016874292.1:p.Asp579Glu
XM_017018805.1:c.693C>A XP_016874294.1:p.Asp231Glu
XM_024448837.1:c.966C>A XP_024304605.1:p.Asp322Glu
XM_024448838.1:c.966C>A XP_024304606.1:p.Asp322Glu
XM_024448839.1:c.966C>A XP_024304607.1:p.Asp322Glu
XM_024448840.1:c.354C>A XP_024304608.1:p.Asp118Glu
XR_001748576.1:n.1946C>A
NM_001370297.1:c.693C>A NP_001357226.1:p.Asp231Glu
NM_001370298.1:c.1737C>A NP_001357227.1:p.Asp579Glu
NM_001304483.2:c.501C>A NP_001291412.1:p.Asp167Glu
NM_001304484.2:c.213C>A NP_001291413.1:p.Asp71Glu
NM_001330373.2:c.966C>A NP_001317302.1:p.Asp322Glu
NM_001330374.2:c.966C>A NP_001317303.1:p.Asp322Glu
NM_001370298.3:c.1656C>A MANE Select NP_001357227.2:p.Asp552Glu
NM_001384126.1:c.1656C>A NP_001371055.1:p.Asp552Glu
NM_001384127.1:c.1245C>A NP_001371056.1:p.Asp415Glu
NM_001384128.1:c.1245C>A NP_001371057.1:p.Asp415Glu
NM_001384130.1:c.966C>A NP_001371059.1:p.Asp322Glu
NM_001385118.1:c.1245C>A NP_001372047.1:p.Asp415Glu