Canonical Allele Identifier: CA2839342408
Gene: FGD4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32582366dup , CM000674.2:g.32582366dup GRCh38
NC_000012.11:g.32735300dup , CM000674.1:g.32735300dup GRCh37
NC_000012.10:g.32626567dup NCBI36
NG_008626.2:g.187838dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000427716.7:c.499dup ENSP00000394487.2:p.Leu167ProfsTer?
ENST00000531134.7:c.754dup ENSP00000431323.1:p.Leu252ProfsTer?
ENST00000583694.2:c.499dup ENSP00000462623.2:p.Leu167ProfsTer?
ENST00000682739.1:c.220dup ENSP00000507616.1:p.Leu74ProfsTer?
ENST00000683182.1:c.-449-16131dup ENSP00000507831.1:n.-449-16131dup
ENST00000683515.1:n.6dup
ENST00000525053.6:c.499dup ENSP00000433666.2:p.Leu167ProfsTer?
ENST00000531134.6:c.754dup ENSP00000431323.1:p.Leu252ProfsTer?
ENST00000534526.7:c.910dup MANE Select ENSP00000449273.1:p.Leu304ProfsTer?
ENST00000395740.5:c.499dup ENSP00000379089.1:p.Leu167ProfsTer?
ENST00000427716.6:c.499dup ENSP00000394487.2:p.Leu167ProfsTer?
ENST00000472289.5:c.499dup ENSP00000434356.1:p.Leu167ProfsTer?
ENST00000493087.5:c.499dup ENSP00000437109.1:p.Leu167ProfsTer?
ENST00000494275.5:n.850dup
ENST00000525053.5:c.835dup ENSP00000433666.1:p.Leu279ProfsTer?
ENST00000531134.5:c.754dup ENSP00000431323.1:p.Leu252ProfsTer?
ENST00000534526.6:c.910dup ENSP00000449273.1:p.Leu304ProfsTer?
ENST00000546442.5:c.220dup ENSP00000446695.1:p.Leu74ProfsTer?
ENST00000551984.5:c.92+5917dup ENSP00000449614.1:n.92+5917dup
NM_001304480.1:c.835dup NP_001291409.1:p.Leu279ProfsTer?
NM_001304481.1:c.754dup NP_001291410.1:p.Leu252ProfsTer?
NM_001304483.1:c.-346dup NP_001291412.1:n.-346dup
NM_001304484.1:c.-653dup NP_001291413.1:n.-653dup
NM_139241.3:c.499dup NP_640334.2:p.Leu167ProfsTer?
XM_005253304.3:c.991dup XP_005253361.1:p.Leu331ProfsTer?
XM_005253307.2:c.220dup XP_005253364.1:p.Leu74ProfsTer?
XM_005253308.3:c.220dup XP_005253365.1:p.Leu74ProfsTer?
XM_005253309.1:c.220dup XP_005253366.1:p.Leu74ProfsTer?
XM_011520554.1:c.793dup XP_011518856.1:p.Leu265ProfsTer?
XM_011520555.1:c.499dup XP_011518857.1:p.Leu167ProfsTer?
XM_011520556.1:c.499dup XP_011518858.1:p.Leu167ProfsTer?
XM_011520557.1:c.49-16131dup XP_011518859.1:n.49-16131dup
NM_001330373.1:c.220dup NP_001317302.1:p.Leu74ProfsTer?
NM_001330374.1:c.220dup NP_001317303.1:p.Leu74ProfsTer?
XM_005253304.4:c.991dup XP_005253361.1:p.Leu331ProfsTer?
XM_005253308.5:c.220dup XP_005253365.1:p.Leu74ProfsTer?
XM_005253310.4:c.-346dup XP_005253367.1:n.-346dup
XM_017018803.1:c.991dup XP_016874292.1:p.Leu331ProfsTer?
XM_017018805.1:c.49-16131dup XP_016874294.1:n.49-16131dup
XM_024448837.1:c.220dup XP_024304605.1:p.Leu74ProfsTer?
XM_024448838.1:c.220dup XP_024304606.1:p.Leu74ProfsTer?
XM_024448839.1:c.220dup XP_024304607.1:p.Leu74ProfsTer?
XM_024448840.1:c.-202-16131dup XP_024304608.1:n.-202-16131dup
XR_001748576.1:n.1181dup
NM_001370297.1:c.49-16131dup NP_001357226.1:n.49-16131dup
NM_001370298.1:c.991dup NP_001357227.1:p.Leu331ProfsTer?
NM_001304483.2:c.-346dup NP_001291412.1:n.-346dup
NM_001304484.2:c.-653dup NP_001291413.1:n.-653dup
NM_001330373.2:c.220dup NP_001317302.1:p.Leu74ProfsTer?
NM_001330374.2:c.220dup NP_001317303.1:p.Leu74ProfsTer?
NM_001370298.3:c.910dup MANE Select NP_001357227.2:p.Leu304ProfsTer?
NM_001384126.1:c.910dup NP_001371055.1:p.Leu304ProfsTer?
NM_001384127.1:c.499dup NP_001371056.1:p.Leu167ProfsTer?
NM_001384128.1:c.499dup NP_001371057.1:p.Leu167ProfsTer?
NM_001384130.1:c.220dup NP_001371059.1:p.Leu74ProfsTer?
NM_001384131.1:c.499dup NP_001371060.1:p.Leu167ProfsTer?
NM_001384132.1:c.499dup NP_001371061.1:p.Leu167ProfsTer?
NM_001385118.1:c.499dup NP_001372047.1:p.Leu167ProfsTer?
NR_168884.1:n.736dup