Canonical Allele Identifier: CA2026256403
Gene: FGD4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32601315G= , CM000674.2:g.32601315G= GRCh38
NC_000012.11:g.32754249G= , CM000674.1:g.32754249G= GRCh37
NC_000012.10:g.32645516G= NCBI36
NG_008626.2:g.206787G=

Transcript Alleles

HGVS Amino-acid change
ENST00000427716.7:c.728G= ENSP00000394487.2:p.Gly243=
ENST00000531134.7:c.983G= ENSP00000431323.1:p.Gly328=
ENST00000583694.2:c.728G= ENSP00000462623.2:p.Gly243=
ENST00000682739.1:c.449G= ENSP00000507616.1:p.Gly150=
ENST00000683182.1:c.-322G= ENSP00000507831.1:n.-322G=
ENST00000683515.1:n.235G=
ENST00000525053.6:c.728G= ENSP00000433666.2:p.Gly243=
ENST00000531134.6:c.983G= ENSP00000431323.1:p.Gly328=
ENST00000534526.7:c.1139G= MANE Select ENSP00000449273.1:p.Gly380=
ENST00000395740.5:c.*120G= ENSP00000379089.1:n.*120G=
ENST00000427716.6:c.728G= ENSP00000394487.2:p.Gly243=
ENST00000493087.5:c.*120G= ENSP00000437109.1:n.*120G=
ENST00000494977.1:c.317G=
ENST00000525053.5:c.1064G= ENSP00000433666.1:p.Gly355=
ENST00000531134.5:c.983G= ENSP00000431323.1:p.Gly328=
ENST00000534526.6:c.1139G= ENSP00000449273.1:p.Gly380=
ENST00000546442.5:c.449G= ENSP00000446695.1:p.Gly150=
ENST00000551984.5:c.*97G= ENSP00000449614.1:n.*97G=
NM_001304480.1:c.1064G= NP_001291409.1:p.Gly355=
NM_001304481.1:c.983G= NP_001291410.1:p.Gly328=
NM_001304483.1:c.-17G= NP_001291412.1:n.-17G=
NM_001304484.1:c.-324G= NP_001291413.1:n.-324G=
NM_139241.3:c.728G= NP_640334.2:p.Gly243=
XM_005253304.3:c.1220G= XP_005253361.1:p.Gly407=
XM_005253307.2:c.449G= XP_005253364.1:p.Gly150=
XM_005253308.3:c.449G= XP_005253365.1:p.Gly150=
XM_005253309.1:c.449G= XP_005253366.1:p.Gly150=
XM_005253310.3:c.-17G= XP_005253367.1:n.-17G=
XM_011520554.1:c.1022G= XP_011518856.1:p.Gly341=
XM_011520555.1:c.728G= XP_011518857.1:p.Gly243=
XM_011520556.1:c.728G= XP_011518858.1:p.Gly243=
XM_011520557.1:c.176G= XP_011518859.1:p.Gly59=
XM_011520558.1:c.131G= XP_011518860.1:p.Gly44=
XM_011520559.1:c.52G= XP_011518861.1:p.Ala18=
NM_001330373.1:c.449G= NP_001317302.1:p.Gly150=
NM_001330374.1:c.449G= NP_001317303.1:p.Gly150=
XM_005253304.4:c.1220G= XP_005253361.1:p.Gly407=
XM_005253308.5:c.449G= XP_005253365.1:p.Gly150=
XM_005253310.4:c.-17G= XP_005253367.1:n.-17G=
XM_011520558.2:c.131G= XP_011518860.1:p.Gly44=
XM_011520559.3:c.52G= XP_011518861.1:p.Ala18=
XM_017018803.1:c.1220G= XP_016874292.1:p.Gly407=
XM_017018805.1:c.176G= XP_016874294.1:p.Gly59=
XM_024448837.1:c.449G= XP_024304605.1:p.Gly150=
XM_024448838.1:c.449G= XP_024304606.1:p.Gly150=
XM_024448839.1:c.449G= XP_024304607.1:p.Gly150=
XM_024448840.1:c.-75G= XP_024304608.1:n.-75G=
XR_001748576.1:n.1410G=
NM_001370297.1:c.176G= NP_001357226.1:p.Gly59=
NM_001370298.1:c.1220G= NP_001357227.1:p.Gly407=
NM_001304483.2:c.-17G= NP_001291412.1:n.-17G=
NM_001304484.2:c.-324G= NP_001291413.1:n.-324G=
NM_001330373.2:c.449G= NP_001317302.1:p.Gly150=
NM_001330374.2:c.449G= NP_001317303.1:p.Gly150=
NM_001370298.3:c.1139G= MANE Select NP_001357227.2:p.Gly380=
NM_001384126.1:c.1139G= NP_001371055.1:p.Gly380=
NM_001384127.1:c.728G= NP_001371056.1:p.Gly243=
NM_001384128.1:c.728G= NP_001371057.1:p.Gly243=
NM_001384130.1:c.449G= NP_001371059.1:p.Gly150=
NM_001385118.1:c.728G= NP_001372047.1:p.Gly243=