Canonical Allele Identifier: CA339862
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1017
dbSNP Id: rs281865065

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32633547A>G , CM000674.2:g.32633547A>G GRCh38
NC_000012.11:g.32786481A>G , CM000674.1:g.32786481A>G GRCh37
NC_000012.10:g.32677748A>G NCBI36
NG_008626.2:g.239019A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000427716.7:c.1762-2A>G ENSP00000394487.2:n.1762-2A>G
ENST00000531134.7:c.2017-2A>G ENSP00000431323.1:n.2017-2A>G
ENST00000583694.2:c.1762-2A>G ENSP00000462623.2:n.1762-2A>G
ENST00000682739.1:c.1483-2A>G ENSP00000507616.1:n.1483-2A>G
ENST00000683182.1:c.574-2A>G ENSP00000507831.1:n.574-2A>G
ENST00000684033.1:n.560-2A>G
ENST00000525053.6:c.1762-2A>G ENSP00000433666.2:n.1762-2A>G
ENST00000531134.6:c.2017-2A>G ENSP00000431323.1:n.2017-2A>G
ENST00000534526.7:c.2173-2A>G MANE Select ENSP00000449273.1:n.2173-2A>G
ENST00000395740.5:c.*1154-2A>G ENSP00000379089.1:n.*1154-2A>G
ENST00000427716.6:c.1762-2A>G ENSP00000394487.2:n.1762-2A>G
ENST00000493087.5:c.*1173-2A>G ENSP00000437109.1:n.*1173-2A>G
ENST00000494977.1:c.1444-2A>G
ENST00000525053.5:c.2098-2A>G ENSP00000433666.1:n.2098-2A>G
ENST00000531134.5:c.2017-2A>G ENSP00000431323.1:n.2017-2A>G
ENST00000534526.6:c.2173-2A>G ENSP00000449273.1:n.2173-2A>G
ENST00000546442.5:c.1483-2A>G ENSP00000446695.1:n.1483-2A>G
ENST00000551984.5:c.*1131-2A>G ENSP00000449614.1:n.*1131-2A>G
NM_001304480.1:c.2098-2A>G NP_001291409.1:n.2098-2A>G
NM_001304481.1:c.2017-2A>G NP_001291410.1:n.2017-2A>G
NM_001304483.1:c.1018-2A>G NP_001291412.1:n.1018-2A>G
NM_001304484.1:c.730-2A>G NP_001291413.1:n.730-2A>G
NM_139241.3:c.1762-2A>G NP_640334.2:n.1762-2A>G
XM_005253304.3:c.2254-2A>G XP_005253361.1:n.2254-2A>G
XM_005253307.2:c.1483-2A>G XP_005253364.1:n.1483-2A>G
XM_005253308.3:c.1483-2A>G XP_005253365.1:n.1483-2A>G
XM_005253309.1:c.1483-2A>G XP_005253366.1:n.1483-2A>G
XM_005253310.3:c.1018-2A>G XP_005253367.1:n.1018-2A>G
XM_011520554.1:c.2056-2A>G XP_011518856.1:n.2056-2A>G
XM_011520555.1:c.1762-2A>G XP_011518857.1:n.1762-2A>G
XM_011520556.1:c.1762-2A>G XP_011518858.1:n.1762-2A>G
XM_011520557.1:c.1210-2A>G XP_011518859.1:n.1210-2A>G
XM_011520558.1:c.1165-2A>G XP_011518860.1:n.1165-2A>G
XM_011520559.1:c.997-2A>G XP_011518861.1:n.997-2A>G
NM_001330373.1:c.1483-2A>G NP_001317302.1:n.1483-2A>G
NM_001330374.1:c.1483-2A>G NP_001317303.1:n.1483-2A>G
XM_005253304.4:c.2254-2A>G XP_005253361.1:n.2254-2A>G
XM_005253308.5:c.1483-2A>G XP_005253365.1:n.1483-2A>G
XM_005253310.4:c.1018-2A>G XP_005253367.1:n.1018-2A>G
XM_011520558.2:c.1165-2A>G XP_011518860.1:n.1165-2A>G
XM_011520559.3:c.997-2A>G XP_011518861.1:n.997-2A>G
XM_017018803.1:c.2254-2A>G XP_016874292.1:n.2254-2A>G
XM_017018805.1:c.1210-2A>G XP_016874294.1:n.1210-2A>G
XM_024448837.1:c.1483-2A>G XP_024304605.1:n.1483-2A>G
XM_024448838.1:c.1483-2A>G XP_024304606.1:n.1483-2A>G
XM_024448839.1:c.1483-2A>G XP_024304607.1:n.1483-2A>G
XM_024448840.1:c.871-2A>G XP_024304608.1:n.871-2A>G
NM_001370297.1:c.1210-2A>G NP_001357226.1:n.1210-2A>G
NM_001370298.1:c.2254-2A>G NP_001357227.1:n.2254-2A>G
NM_001304483.2:c.1018-2A>G NP_001291412.1:n.1018-2A>G
NM_001304484.2:c.730-2A>G NP_001291413.1:n.730-2A>G
NM_001330373.2:c.1483-2A>G NP_001317302.1:n.1483-2A>G
NM_001330374.2:c.1483-2A>G NP_001317303.1:n.1483-2A>G
NM_001370298.3:c.2173-2A>G MANE Select NP_001357227.2:n.2173-2A>G
NM_001384126.1:c.2173-2A>G NP_001371055.1:n.2173-2A>G
NM_001384127.1:c.1762-2A>G NP_001371056.1:n.1762-2A>G
NM_001384128.1:c.1762-2A>G NP_001371057.1:n.1762-2A>G
NM_001384130.1:c.1483-2A>G NP_001371059.1:n.1483-2A>G
NM_001385118.1:c.1762-2A>G NP_001372047.1:n.1762-2A>G