Canonical Allele Identifier: CA645577289
Gene: FGD4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32582180_32582182del , CM000674.2:g.32582180_32582182del GRCh38
NC_000012.11:g.32735114_32735116del , CM000674.1:g.32735114_32735116del GRCh37
NC_000012.10:g.32626381_32626383del NCBI36
NG_008626.2:g.187652_187654del

Transcript Alleles

HGVS Amino-acid Change
ENST00000427716.7:c.313_315del ENSP00000394487.2:p.Glu105del
ENST00000531134.7:c.568_570del ENSP00000431323.1:p.Glu190del
ENST00000583694.2:c.313_315del ENSP00000462623.2:p.Glu105del
ENST00000682739.1:c.34_36del ENSP00000507616.1:p.Glu12del
ENST00000683182.1:c.-449-16317_-449-16315del ENSP00000507831.1:n.-449-16317_-449-16315del
ENST00000525053.6:c.313_315del ENSP00000433666.2:p.Glu105del
ENST00000531134.6:c.568_570del ENSP00000431323.1:p.Glu190del
ENST00000534526.7:c.724_726del MANE Select ENSP00000449273.1:p.Glu242del
ENST00000395740.5:c.313_315del ENSP00000379089.1:p.Glu105del
ENST00000427716.6:c.313_315del ENSP00000394487.2:p.Glu105del
ENST00000472289.5:c.313_315del ENSP00000434356.1:p.Glu105del
ENST00000493087.5:c.313_315del ENSP00000437109.1:p.Glu105del
ENST00000494275.5:n.664_666del
ENST00000525053.5:c.649_651del ENSP00000433666.1:p.Glu217del
ENST00000531134.5:c.568_570del ENSP00000431323.1:p.Glu190del
ENST00000534526.6:c.724_726del ENSP00000449273.1:p.Glu242del
ENST00000546442.5:c.34_36del ENSP00000446695.1:p.Glu12del
ENST00000550091.5:n.478_480del
ENST00000551984.5:c.92+5731_92+5733del ENSP00000449614.1:n.92+5731_92+5733del
NM_001304480.1:c.649_651del NP_001291409.1:p.Glu217del
NM_001304481.1:c.568_570del NP_001291410.1:p.Glu190del
NM_001304483.1:c.-532_-530del NP_001291412.1:n.-532_-530del
NM_001304484.1:c.-839_-837del NP_001291413.1:n.-839_-837del
NM_139241.3:c.313_315del NP_640334.2:p.Glu105del
XM_005253304.3:c.805_807del XP_005253361.1:p.Glu269del
XM_005253307.2:c.34_36del XP_005253364.1:p.Glu12del
XM_005253308.3:c.34_36del XP_005253365.1:p.Glu12del
XM_005253309.1:c.34_36del XP_005253366.1:p.Glu12del
XM_011520554.1:c.607_609del XP_011518856.1:p.Glu203del
XM_011520555.1:c.313_315del XP_011518857.1:p.Glu105del
XM_011520556.1:c.313_315del XP_011518858.1:p.Glu105del
XM_011520557.1:c.49-16317_49-16315del XP_011518859.1:n.49-16317_49-16315del
NM_001330373.1:c.34_36del NP_001317302.1:p.Glu12del
NM_001330374.1:c.34_36del NP_001317303.1:p.Glu12del
XM_005253304.4:c.805_807del XP_005253361.1:p.Glu269del
XM_005253308.5:c.34_36del XP_005253365.1:p.Glu12del
XM_005253310.4:c.-532_-530del XP_005253367.1:n.-532_-530del
XM_017018803.1:c.805_807del XP_016874292.1:p.Glu269del
XM_017018805.1:c.49-16317_49-16315del XP_016874294.1:n.49-16317_49-16315del
XM_024448837.1:c.34_36del XP_024304605.1:p.Glu12del
XM_024448838.1:c.34_36del XP_024304606.1:p.Glu12del
XM_024448839.1:c.34_36del XP_024304607.1:p.Glu12del
XM_024448840.1:c.-202-16317_-202-16315del XP_024304608.1:n.-202-16317_-202-16315del
XR_001748576.1:n.995_997del
NM_001370297.1:c.49-16317_49-16315del NP_001357226.1:n.49-16317_49-16315del
NM_001370298.1:c.805_807del NP_001357227.1:p.Glu269del
NM_001304483.2:c.-532_-530del NP_001291412.1:n.-532_-530del
NM_001304484.2:c.-839_-837del NP_001291413.1:n.-839_-837del
NM_001330373.2:c.34_36del NP_001317302.1:p.Glu12del
NM_001330374.2:c.34_36del NP_001317303.1:p.Glu12del
NM_001370298.3:c.724_726del MANE Select NP_001357227.2:p.Glu242del
NM_001384126.1:c.724_726del NP_001371055.1:p.Glu242del
NM_001384127.1:c.313_315del NP_001371056.1:p.Glu105del
NM_001384128.1:c.313_315del NP_001371057.1:p.Glu105del
NM_001384130.1:c.34_36del NP_001371059.1:p.Glu12del
NM_001384131.1:c.313_315del NP_001371060.1:p.Glu105del
NM_001384132.1:c.313_315del NP_001371061.1:p.Glu105del
NM_001385118.1:c.313_315del NP_001372047.1:p.Glu105del
NR_168884.1:n.550_552del