Canonical Allele Identifier: CA645577290

Gene: FGD4

Linked Data

• COSMIC: COSM6136772

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32582431_32582432delinsAT , CM000674.2:g.32582431_32582432delinsAT	GRCh38
NC_000012.11:g.32735365_32735366delinsAT , CM000674.1:g.32735365_32735366delinsAT	GRCh37
NC_000012.10:g.32626632_32626633delinsAT	NCBI36
NG_008626.2:g.187903_187904delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427716.7:c.564_565delinsAT	ENSP00000394487.2:p.Leu189Ter
ENST00000531134.7:c.819_820delinsAT	ENSP00000431323.1:p.Leu274Ter
ENST00000583694.2:c.564_565delinsAT	ENSP00000462623.2:p.Leu189Ter
ENST00000682739.1:c.285_286delinsAT	ENSP00000507616.1:p.Leu96Ter
ENST00000683182.1:c.-449-16066_-449-16065delinsAT	ENSP00000507831.1:n.-449-16066_-449-16065delinsAT
ENST00000683515.1:n.71_72delinsAT
ENST00000525053.6:c.564_565delinsAT	ENSP00000433666.2:p.Leu189Ter
ENST00000531134.6:c.819_820delinsAT	ENSP00000431323.1:p.Leu274Ter
ENST00000534526.7:c.975_976delinsAT MANE Select	ENSP00000449273.1:p.Leu326Ter
ENST00000395740.5:c.564_565delinsAT	ENSP00000379089.1:p.Leu189Ter
ENST00000427716.6:c.564_565delinsAT	ENSP00000394487.2:p.Leu189Ter
ENST00000472289.5:c.564_565delinsAT	ENSP00000434356.1:p.Leu189Ter
ENST00000493087.5:c.564_565delinsAT	ENSP00000437109.1:p.Leu189Ter
ENST00000494275.5:n.915_916delinsAT
ENST00000494977.1:c.53_54delinsAT
ENST00000525053.5:c.900_901delinsAT	ENSP00000433666.1:p.Leu301Ter
ENST00000531134.5:c.819_820delinsAT	ENSP00000431323.1:p.Leu274Ter
ENST00000534526.6:c.975_976delinsAT	ENSP00000449273.1:p.Leu326Ter
ENST00000546442.5:c.285_286delinsAT	ENSP00000446695.1:p.Leu96Ter
ENST00000551984.5:c.92+5982_92+5983delinsAT	ENSP00000449614.1:n.92+5982_92+5983delinsAT
NM_001304480.1:c.900_901delinsAT	NP_001291409.1:p.Leu301Ter
NM_001304481.1:c.819_820delinsAT	NP_001291410.1:p.Leu274Ter
NM_001304483.1:c.-281_-280delinsAT	NP_001291412.1:n.-281_-280delinsAT
NM_001304484.1:c.-588_-587delinsAT	NP_001291413.1:n.-588_-587delinsAT
NM_139241.3:c.564_565delinsAT	NP_640334.2:p.Leu189Ter
XM_005253304.3:c.1056_1057delinsAT	XP_005253361.1:p.Leu353Ter
XM_005253307.2:c.285_286delinsAT	XP_005253364.1:p.Leu96Ter
XM_005253308.3:c.285_286delinsAT	XP_005253365.1:p.Leu96Ter
XM_005253309.1:c.285_286delinsAT	XP_005253366.1:p.Leu96Ter
XM_011520554.1:c.858_859delinsAT	XP_011518856.1:p.Leu287Ter
XM_011520555.1:c.564_565delinsAT	XP_011518857.1:p.Leu189Ter
XM_011520556.1:c.564_565delinsAT	XP_011518858.1:p.Leu189Ter
XM_011520557.1:c.49-16066_49-16065delinsAT	XP_011518859.1:n.49-16066_49-16065delinsAT
NM_001330373.1:c.285_286delinsAT	NP_001317302.1:p.Leu96Ter
NM_001330374.1:c.285_286delinsAT	NP_001317303.1:p.Leu96Ter
XM_005253304.4:c.1056_1057delinsAT	XP_005253361.1:p.Leu353Ter
XM_005253308.5:c.285_286delinsAT	XP_005253365.1:p.Leu96Ter
XM_005253310.4:c.-281_-280delinsAT	XP_005253367.1:n.-281_-280delinsAT
XM_017018803.1:c.1056_1057delinsAT	XP_016874292.1:p.Leu353Ter
XM_017018805.1:c.49-16066_49-16065delinsAT	XP_016874294.1:n.49-16066_49-16065delinsAT
XM_024448837.1:c.285_286delinsAT	XP_024304605.1:p.Leu96Ter
XM_024448838.1:c.285_286delinsAT	XP_024304606.1:p.Leu96Ter
XM_024448839.1:c.285_286delinsAT	XP_024304607.1:p.Leu96Ter
XM_024448840.1:c.-202-16066_-202-16065delinsAT	XP_024304608.1:n.-202-16066_-202-16065delinsAT
XR_001748576.1:n.1246_1247delinsAT
NM_001370297.1:c.49-16066_49-16065delinsAT	NP_001357226.1:n.49-16066_49-16065delinsAT
NM_001370298.1:c.1056_1057delinsAT	NP_001357227.1:p.Leu353Ter
NM_001304483.2:c.-281_-280delinsAT	NP_001291412.1:n.-281_-280delinsAT
NM_001304484.2:c.-588_-587delinsAT	NP_001291413.1:n.-588_-587delinsAT
NM_001330373.2:c.285_286delinsAT	NP_001317302.1:p.Leu96Ter
NM_001330374.2:c.285_286delinsAT	NP_001317303.1:p.Leu96Ter
NM_001370298.3:c.975_976delinsAT MANE Select	NP_001357227.2:p.Leu326Ter
NM_001384126.1:c.975_976delinsAT	NP_001371055.1:p.Leu326Ter
NM_001384127.1:c.564_565delinsAT	NP_001371056.1:p.Leu189Ter
NM_001384128.1:c.564_565delinsAT	NP_001371057.1:p.Leu189Ter
NM_001384130.1:c.285_286delinsAT	NP_001371059.1:p.Leu96Ter
NM_001384131.1:c.564_565delinsAT	NP_001371060.1:p.Leu189Ter
NM_001384132.1:c.564_565delinsAT	NP_001371061.1:p.Leu189Ter
NM_001385118.1:c.564_565delinsAT	NP_001372047.1:p.Leu189Ter
NR_168884.1:n.801_802delinsAT