Canonical Allele Identifier: CA235235948

Gene: FGD4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32625289_32625290insTA , CM000674.2:g.32625289_32625290insTA	GRCh38
NC_000012.11:g.32778223_32778224insTA , CM000674.1:g.32778223_32778224insTA	GRCh37
NC_000012.10:g.32669490_32669491insTA	NCBI36
NG_008626.2:g.230761_230762insTA

Transcript Alleles

HGVS	Amino-acid Change
NM_001370298.3:c.2046+221_2046+222insTA MANE Select	NP_001357227.2:n.2046+221_2046+222insTA
ENST00000534526.7:c.2046+221_2046+222insTA MANE Select	ENSP00000449273.1:n.2046+221_2046+222insTA
NM_001304480.1:c.1971+221_1971+222insTA	NP_001291409.1:n.1971+221_1971+222insTA
NM_001304481.1:c.1890+221_1890+222insTA	NP_001291410.1:n.1890+221_1890+222insTA
NM_001304483.1:c.891+221_891+222insTA	NP_001291412.1:n.891+221_891+222insTA
NM_001304483.2:c.891+221_891+222insTA	NP_001291412.1:n.891+221_891+222insTA
NM_001304484.1:c.603+221_603+222insTA	NP_001291413.1:n.603+221_603+222insTA
NM_001304484.2:c.603+221_603+222insTA	NP_001291413.1:n.603+221_603+222insTA
NM_001330373.1:c.1356+221_1356+222insTA	NP_001317302.1:n.1356+221_1356+222insTA
NM_001330373.2:c.1356+221_1356+222insTA	NP_001317302.1:n.1356+221_1356+222insTA
NM_001330374.1:c.1356+221_1356+222insTA	NP_001317303.1:n.1356+221_1356+222insTA
NM_001330374.2:c.1356+221_1356+222insTA	NP_001317303.1:n.1356+221_1356+222insTA
NM_001370297.1:c.1083+221_1083+222insTA	NP_001357226.1:n.1083+221_1083+222insTA
NM_001370298.1:c.2127+221_2127+222insTA	NP_001357227.1:n.2127+221_2127+222insTA
NM_001384126.1:c.2046+221_2046+222insTA	NP_001371055.1:n.2046+221_2046+222insTA
NM_001384127.1:c.1635+221_1635+222insTA	NP_001371056.1:n.1635+221_1635+222insTA
NM_001384128.1:c.1635+221_1635+222insTA	NP_001371057.1:n.1635+221_1635+222insTA
NM_001384130.1:c.1356+221_1356+222insTA	NP_001371059.1:n.1356+221_1356+222insTA
NM_001385118.1:c.1635+221_1635+222insTA	NP_001372047.1:n.1635+221_1635+222insTA
NM_139241.3:c.1635+221_1635+222insTA	NP_640334.2:n.1635+221_1635+222insTA
ENST00000395740.5:c.*1027+221_*1027+222insTA	ENSP00000379089.1:n.*1027+221_*1027+222insTA
ENST00000427716.6:c.1635+221_1635+222insTA	ENSP00000394487.2:n.1635+221_1635+222insTA
ENST00000427716.7:c.1635+221_1635+222insTA	ENSP00000394487.2:n.1635+221_1635+222insTA
ENST00000493087.5:c.*1046+221_*1046+222insTA	ENSP00000437109.1:n.*1046+221_*1046+222insTA
ENST00000494977.1:c.1317+221_1317+222insTA
ENST00000525053.5:c.1971+221_1971+222insTA	ENSP00000433666.1:n.1971+221_1971+222insTA
ENST00000525053.6:c.1635+221_1635+222insTA	ENSP00000433666.2:n.1635+221_1635+222insTA
ENST00000531134.5:c.1890+221_1890+222insTA	ENSP00000431323.1:n.1890+221_1890+222insTA
ENST00000531134.6:c.1890+221_1890+222insTA	ENSP00000431323.1:n.1890+221_1890+222insTA
ENST00000531134.7:c.1890+221_1890+222insTA	ENSP00000431323.1:n.1890+221_1890+222insTA
ENST00000534526.6:c.2046+221_2046+222insTA	ENSP00000449273.1:n.2046+221_2046+222insTA
ENST00000546442.5:c.1356+221_1356+222insTA	ENSP00000446695.1:n.1356+221_1356+222insTA
ENST00000551984.5:c.*1004+221_*1004+222insTA	ENSP00000449614.1:n.*1004+221_*1004+222insTA
ENST00000583694.2:c.1635+221_1635+222insTA	ENSP00000462623.2:n.1635+221_1635+222insTA
ENST00000682739.1:c.1356+221_1356+222insTA	ENSP00000507616.1:n.1356+221_1356+222insTA
ENST00000683182.1:c.447+221_447+222insTA	ENSP00000507831.1:n.447+221_447+222insTA
ENST00000683515.1:n.1142+221_1142+222insTA
ENST00000684033.1:n.433+221_433+222insTA
XM_005253304.3:c.2127+221_2127+222insTA	XP_005253361.1:n.2127+221_2127+222insTA
XM_005253304.4:c.2127+221_2127+222insTA	XP_005253361.1:n.2127+221_2127+222insTA
XM_005253307.2:c.1356+221_1356+222insTA	XP_005253364.1:n.1356+221_1356+222insTA
XM_005253308.3:c.1356+221_1356+222insTA	XP_005253365.1:n.1356+221_1356+222insTA
XM_005253308.5:c.1356+221_1356+222insTA	XP_005253365.1:n.1356+221_1356+222insTA
XM_005253309.1:c.1356+221_1356+222insTA	XP_005253366.1:n.1356+221_1356+222insTA
XM_005253310.3:c.891+221_891+222insTA	XP_005253367.1:n.891+221_891+222insTA
XM_005253310.4:c.891+221_891+222insTA	XP_005253367.1:n.891+221_891+222insTA
XM_011520554.1:c.1929+221_1929+222insTA	XP_011518856.1:n.1929+221_1929+222insTA
XM_011520555.1:c.1635+221_1635+222insTA	XP_011518857.1:n.1635+221_1635+222insTA
XM_011520556.1:c.1635+221_1635+222insTA	XP_011518858.1:n.1635+221_1635+222insTA
XM_011520557.1:c.1083+221_1083+222insTA	XP_011518859.1:n.1083+221_1083+222insTA
XM_011520558.1:c.1038+221_1038+222insTA	XP_011518860.1:n.1038+221_1038+222insTA
XM_011520558.2:c.1038+221_1038+222insTA	XP_011518860.1:n.1038+221_1038+222insTA
XM_011520559.1:c.870+221_870+222insTA	XP_011518861.1:n.870+221_870+222insTA
XM_011520559.3:c.870+221_870+222insTA	XP_011518861.1:n.870+221_870+222insTA
XM_017018803.1:c.2127+221_2127+222insTA	XP_016874292.1:n.2127+221_2127+222insTA
XM_017018805.1:c.1083+221_1083+222insTA	XP_016874294.1:n.1083+221_1083+222insTA
XM_024448837.1:c.1356+221_1356+222insTA	XP_024304605.1:n.1356+221_1356+222insTA
XM_024448838.1:c.1356+221_1356+222insTA	XP_024304606.1:n.1356+221_1356+222insTA
XM_024448839.1:c.1356+221_1356+222insTA	XP_024304607.1:n.1356+221_1356+222insTA
XM_024448840.1:c.744+221_744+222insTA	XP_024304608.1:n.744+221_744+222insTA