Canonical Allele Identifier: CA2026230720
Gene: FGD4 HGNC NCBI

Linked Data

dbSNP Id: rs1946668238

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32582179_32582180insTTTTTGTTGAGGT , CM000674.2:g.32582179_32582180insTTTTTGTTGAGGT GRCh38
NC_000012.11:g.32735113_32735114insTTTTTGTTGAGGT , CM000674.1:g.32735113_32735114insTTTTTGTTGAGGT GRCh37
NC_000012.10:g.32626380_32626381insTTTTTGTTGAGGT NCBI36
NG_008626.2:g.187651_187652insTTTTTGTTGAGGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000427716.7:c.312_313insTTTTTGTTGAGGT ENSP00000394487.2:p.Glu105PhefsTer5
ENST00000531134.7:c.567_568insTTTTTGTTGAGGT ENSP00000431323.1:p.Glu190PhefsTer5
ENST00000583694.2:c.312_313insTTTTTGTTGAGGT ENSP00000462623.2:p.Glu105PhefsTer5
ENST00000682739.1:c.33_34insTTTTTGTTGAGGT ENSP00000507616.1:p.Glu12PhefsTer5
ENST00000683182.1:c.-449-16318_-449-16317insTTTTTGTTGAGGT ENSP00000507831.1:n.-449-16318_-449-16317insTTTTTGTTGAGGT
ENST00000525053.6:c.312_313insTTTTTGTTGAGGT ENSP00000433666.2:p.Glu105PhefsTer5
ENST00000531134.6:c.567_568insTTTTTGTTGAGGT ENSP00000431323.1:p.Glu190PhefsTer5
ENST00000534526.7:c.723_724insTTTTTGTTGAGGT MANE Select ENSP00000449273.1:p.Glu242PhefsTer5
ENST00000395740.5:c.312_313insTTTTTGTTGAGGT ENSP00000379089.1:p.Glu105PhefsTer5
ENST00000427716.6:c.312_313insTTTTTGTTGAGGT ENSP00000394487.2:p.Glu105PhefsTer5
ENST00000472289.5:c.312_313insTTTTTGTTGAGGT ENSP00000434356.1:p.Glu105PhefsTer5
ENST00000493087.5:c.312_313insTTTTTGTTGAGGT ENSP00000437109.1:p.Glu105PhefsTer5
ENST00000494275.5:n.663_664insTTTTTGTTGAGGT
ENST00000525053.5:c.648_649insTTTTTGTTGAGGT ENSP00000433666.1:p.Glu217PhefsTer5
ENST00000531134.5:c.567_568insTTTTTGTTGAGGT ENSP00000431323.1:p.Glu190PhefsTer5
ENST00000534526.6:c.723_724insTTTTTGTTGAGGT ENSP00000449273.1:p.Glu242PhefsTer5
ENST00000546442.5:c.33_34insTTTTTGTTGAGGT ENSP00000446695.1:p.Glu12PhefsTer5
ENST00000550091.5:n.477_478insTTTTTGTTGAGGT
ENST00000551984.5:c.92+5730_92+5731insTTTTTGTTGAGGT ENSP00000449614.1:n.92+5730_92+5731insTTTTTGTTGAGGT
NM_001304480.1:c.648_649insTTTTTGTTGAGGT NP_001291409.1:p.Glu217PhefsTer5
NM_001304481.1:c.567_568insTTTTTGTTGAGGT NP_001291410.1:p.Glu190PhefsTer5
NM_001304483.1:c.-533_-532insTTTTTGTTGAGGT NP_001291412.1:n.-533_-532insTTTTTGTTGAGGT
NM_001304484.1:c.-840_-839insTTTTTGTTGAGGT NP_001291413.1:n.-840_-839insTTTTTGTTGAGGT
NM_139241.3:c.312_313insTTTTTGTTGAGGT NP_640334.2:p.Glu105PhefsTer5
XM_005253304.3:c.804_805insTTTTTGTTGAGGT XP_005253361.1:p.Glu269PhefsTer5
XM_005253307.2:c.33_34insTTTTTGTTGAGGT XP_005253364.1:p.Glu12PhefsTer5
XM_005253308.3:c.33_34insTTTTTGTTGAGGT XP_005253365.1:p.Glu12PhefsTer5
XM_005253309.1:c.33_34insTTTTTGTTGAGGT XP_005253366.1:p.Glu12PhefsTer5
XM_011520554.1:c.606_607insTTTTTGTTGAGGT XP_011518856.1:p.Glu203PhefsTer5
XM_011520555.1:c.312_313insTTTTTGTTGAGGT XP_011518857.1:p.Glu105PhefsTer5
XM_011520556.1:c.312_313insTTTTTGTTGAGGT XP_011518858.1:p.Glu105PhefsTer5
XM_011520557.1:c.49-16318_49-16317insTTTTTGTTGAGGT XP_011518859.1:n.49-16318_49-16317insTTTTTGTTGAGGT
NM_001330373.1:c.33_34insTTTTTGTTGAGGT NP_001317302.1:p.Glu12PhefsTer5
NM_001330374.1:c.33_34insTTTTTGTTGAGGT NP_001317303.1:p.Glu12PhefsTer5
XM_005253304.4:c.804_805insTTTTTGTTGAGGT XP_005253361.1:p.Glu269PhefsTer5
XM_005253308.5:c.33_34insTTTTTGTTGAGGT XP_005253365.1:p.Glu12PhefsTer5
XM_005253310.4:c.-533_-532insTTTTTGTTGAGGT XP_005253367.1:n.-533_-532insTTTTTGTTGAGGT
XM_017018803.1:c.804_805insTTTTTGTTGAGGT XP_016874292.1:p.Glu269PhefsTer5
XM_017018805.1:c.49-16318_49-16317insTTTTTGTTGAGGT XP_016874294.1:n.49-16318_49-16317insTTTTTGTTGAGGT
XM_024448837.1:c.33_34insTTTTTGTTGAGGT XP_024304605.1:p.Glu12PhefsTer5
XM_024448838.1:c.33_34insTTTTTGTTGAGGT XP_024304606.1:p.Glu12PhefsTer5
XM_024448839.1:c.33_34insTTTTTGTTGAGGT XP_024304607.1:p.Glu12PhefsTer5
XM_024448840.1:c.-202-16318_-202-16317insTTTTTGTTGAGGT XP_024304608.1:n.-202-16318_-202-16317insTTTTTGTTGAGGT
XR_001748576.1:n.994_995insTTTTTGTTGAGGT
NM_001370297.1:c.49-16318_49-16317insTTTTTGTTGAGGT NP_001357226.1:n.49-16318_49-16317insTTTTTGTTGAGGT
NM_001370298.1:c.804_805insTTTTTGTTGAGGT NP_001357227.1:p.Glu269PhefsTer5
NM_001304483.2:c.-533_-532insTTTTTGTTGAGGT NP_001291412.1:n.-533_-532insTTTTTGTTGAGGT
NM_001304484.2:c.-840_-839insTTTTTGTTGAGGT NP_001291413.1:n.-840_-839insTTTTTGTTGAGGT
NM_001330373.2:c.33_34insTTTTTGTTGAGGT NP_001317302.1:p.Glu12PhefsTer5
NM_001330374.2:c.33_34insTTTTTGTTGAGGT NP_001317303.1:p.Glu12PhefsTer5
NM_001370298.3:c.723_724insTTTTTGTTGAGGT MANE Select NP_001357227.2:p.Glu242PhefsTer5
NM_001384126.1:c.723_724insTTTTTGTTGAGGT NP_001371055.1:p.Glu242PhefsTer5
NM_001384127.1:c.312_313insTTTTTGTTGAGGT NP_001371056.1:p.Glu105PhefsTer5
NM_001384128.1:c.312_313insTTTTTGTTGAGGT NP_001371057.1:p.Glu105PhefsTer5
NM_001384130.1:c.33_34insTTTTTGTTGAGGT NP_001371059.1:p.Glu12PhefsTer5
NM_001384131.1:c.312_313insTTTTTGTTGAGGT NP_001371060.1:p.Glu105PhefsTer5
NM_001384132.1:c.312_313insTTTTTGTTGAGGT NP_001371061.1:p.Glu105PhefsTer5
NM_001385118.1:c.312_313insTTTTTGTTGAGGT NP_001372047.1:p.Glu105PhefsTer5
NR_168884.1:n.549_550insTTTTTGTTGAGGT