Canonical Allele Identifier: CA10632552
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 308279
ClinVar RCV Id: RCV000282326
dbSNP Id: rs184708096

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32502214G>A , CM000674.2:g.32502214G>A GRCh38
NC_000012.11:g.32655148G>A , CM000674.1:g.32655148G>A GRCh37
NC_000012.10:g.32546415G>A NCBI36
NG_008626.2:g.107686G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000427716.7:c.-492G>A ENSP00000394487.2:n.-492G>A
ENST00000531134.7:c.10+16071G>A ENSP00000431323.1:n.10+16071G>A
ENST00000583694.2:c.-370G>A ENSP00000462623.2:n.-370G>A
ENST00000682739.1:c.-1142G>A ENSP00000507616.1:n.-1142G>A
ENST00000683182.1:c.-727G>A ENSP00000507831.1:n.-727G>A
ENST00000531134.6:c.10+16071G>A ENSP00000431323.1:n.10+16071G>A
ENST00000534526.7:c.167-61923G>A MANE Select ENSP00000449273.1:n.167-61923G>A
ENST00000395740.5:c.-370G>A ENSP00000379089.1:n.-370G>A
ENST00000427716.6:c.-370G>A ENSP00000394487.2:n.-370G>A
ENST00000472289.5:c.-370G>A ENSP00000434356.1:n.-370G>A
ENST00000473513.5:n.54G>A
ENST00000479023.5:n.36G>A
ENST00000493087.5:c.-370G>A ENSP00000437109.1:n.-370G>A
ENST00000494275.5:n.166G>A
ENST00000497153.5:n.84G>A
ENST00000531134.5:c.10+16071G>A ENSP00000431323.1:n.10+16071G>A
ENST00000534526.6:c.167-61923G>A ENSP00000449273.1:n.167-61923G>A
ENST00000546442.5:c.-465G>A ENSP00000446695.1:n.-465G>A
ENST00000550091.5:n.105-61923G>A
ENST00000551984.5:c.-370G>A ENSP00000449614.1:n.-370G>A
NM_001304481.1:c.10+16071G>A NP_001291410.1:n.10+16071G>A
NM_001304483.1:c.-1214G>A NP_001291412.1:n.-1214G>A
NM_001304484.1:c.-1521G>A NP_001291413.1:n.-1521G>A
NM_139241.3:c.-370G>A NP_640334.2:n.-370G>A
XM_005253304.3:c.248-61923G>A XP_005253361.1:n.248-61923G>A
XM_005253307.2:c.-465G>A XP_005253364.1:n.-465G>A
XM_005253309.1:c.-340-61923G>A XP_005253366.1:n.-340-61923G>A
XM_011520556.1:c.-513G>A XP_011518858.1:n.-513G>A
NM_001330373.1:c.-465G>A NP_001317302.1:n.-465G>A
NM_001330374.1:c.-341+16071G>A NP_001317303.1:n.-341+16071G>A
XM_005253304.4:c.248-61923G>A XP_005253361.1:n.248-61923G>A
XM_017018803.1:c.248-61923G>A XP_016874292.1:n.248-61923G>A
XM_024448837.1:c.-999G>A XP_024304605.1:n.-999G>A
XM_024448838.1:c.-798G>A XP_024304606.1:n.-798G>A
XM_024448839.1:c.-1142G>A XP_024304607.1:n.-1142G>A
XM_024448840.1:c.-355-61923G>A XP_024304608.1:n.-355-61923G>A
XR_001748576.1:n.438-61923G>A
NM_001370297.1:c.-230G>A NP_001357226.1:n.-230G>A
NM_001370298.1:c.248-61923G>A NP_001357227.1:n.248-61923G>A
NM_001304483.2:c.-1214G>A NP_001291412.1:n.-1214G>A
NM_001304484.2:c.-1521G>A NP_001291413.1:n.-1521G>A
NM_001330373.2:c.-465G>A NP_001317302.1:n.-465G>A
NM_001330374.2:c.-341+16071G>A NP_001317303.1:n.-341+16071G>A
NM_001370298.3:c.167-61923G>A MANE Select NP_001357227.2:n.167-61923G>A
NM_001384126.1:c.167-61923G>A NP_001371055.1:n.167-61923G>A
NM_001384127.1:c.-370G>A NP_001371056.1:n.-370G>A
NM_001384131.1:c.-370G>A NP_001371060.1:n.-370G>A
NR_168884.1:n.52G>A