Canonical Allele Identifier: CA2026243998

Gene: FGD4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32625737T= , CM000674.2:g.32625737T=	GRCh38
NC_000012.11:g.32778671T= , CM000674.1:g.32778671T=	GRCh37
NC_000012.10:g.32669938T=	NCBI36
NG_008626.2:g.231209T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427716.7:c.1719T=	ENSP00000394487.2:p.Asn573=
ENST00000531134.7:c.1974T=	ENSP00000431323.1:p.Asn658=
ENST00000583694.2:c.1719T=	ENSP00000462623.2:p.Asn573=
ENST00000682739.1:c.1440T=	ENSP00000507616.1:p.Asn480=
ENST00000683182.1:c.531T=	ENSP00000507831.1:p.Asn177=
ENST00000683515.1:n.1226T=
ENST00000684033.1:n.517T=
ENST00000525053.6:c.1719T=	ENSP00000433666.2:p.Asn573=
ENST00000531134.6:c.1974T=	ENSP00000431323.1:p.Asn658=
ENST00000534526.7:c.2130T= MANE Select	ENSP00000449273.1:p.Asn710=
ENST00000395740.5:c.*1111T=	ENSP00000379089.1:n.*1111T=
ENST00000427716.6:c.1719T=	ENSP00000394487.2:p.Asn573=
ENST00000493087.5:c.*1130T=	ENSP00000437109.1:n.*1130T=
ENST00000494977.1:c.1401T=
ENST00000525053.5:c.2055T=	ENSP00000433666.1:p.Asn685=
ENST00000531134.5:c.1974T=	ENSP00000431323.1:p.Asn658=
ENST00000534526.6:c.2130T=	ENSP00000449273.1:p.Asn710=
ENST00000546442.5:c.1440T=	ENSP00000446695.1:p.Asn480=
ENST00000551984.5:c.*1088T=	ENSP00000449614.1:n.*1088T=
NM_001304480.1:c.2055T=	NP_001291409.1:p.Asn685=
NM_001304481.1:c.1974T=	NP_001291410.1:p.Asn658=
NM_001304483.1:c.975T=	NP_001291412.1:p.Asn325=
NM_001304484.1:c.687T=	NP_001291413.1:p.Asn229=
NM_139241.3:c.1719T=	NP_640334.2:p.Asn573=
XM_005253304.3:c.2211T=	XP_005253361.1:p.Asn737=
XM_005253307.2:c.1440T=	XP_005253364.1:p.Asn480=
XM_005253308.3:c.1440T=	XP_005253365.1:p.Asn480=
XM_005253309.1:c.1440T=	XP_005253366.1:p.Asn480=
XM_005253310.3:c.975T=	XP_005253367.1:p.Asn325=
XM_011520554.1:c.2013T=	XP_011518856.1:p.Asn671=
XM_011520555.1:c.1719T=	XP_011518857.1:p.Asn573=
XM_011520556.1:c.1719T=	XP_011518858.1:p.Asn573=
XM_011520557.1:c.1167T=	XP_011518859.1:p.Asn389=
XM_011520558.1:c.1122T=	XP_011518860.1:p.Asn374=
XM_011520559.1:c.954T=	XP_011518861.1:p.Asn318=
NM_001330373.1:c.1440T=	NP_001317302.1:p.Asn480=
NM_001330374.1:c.1440T=	NP_001317303.1:p.Asn480=
XM_005253304.4:c.2211T=	XP_005253361.1:p.Asn737=
XM_005253308.5:c.1440T=	XP_005253365.1:p.Asn480=
XM_005253310.4:c.975T=	XP_005253367.1:p.Asn325=
XM_011520558.2:c.1122T=	XP_011518860.1:p.Asn374=
XM_011520559.3:c.954T=	XP_011518861.1:p.Asn318=
XM_017018803.1:c.2211T=	XP_016874292.1:p.Asn737=
XM_017018805.1:c.1167T=	XP_016874294.1:p.Asn389=
XM_024448837.1:c.1440T=	XP_024304605.1:p.Asn480=
XM_024448838.1:c.1440T=	XP_024304606.1:p.Asn480=
XM_024448839.1:c.1440T=	XP_024304607.1:p.Asn480=
XM_024448840.1:c.828T=	XP_024304608.1:p.Asn276=
NM_001370297.1:c.1167T=	NP_001357226.1:p.Asn389=
NM_001370298.1:c.2211T=	NP_001357227.1:p.Asn737=
NM_001304483.2:c.975T=	NP_001291412.1:p.Asn325=
NM_001304484.2:c.687T=	NP_001291413.1:p.Asn229=
NM_001330373.2:c.1440T=	NP_001317302.1:p.Asn480=
NM_001330374.2:c.1440T=	NP_001317303.1:p.Asn480=
NM_001370298.3:c.2130T= MANE Select	NP_001357227.2:p.Asn710=
NM_001384126.1:c.2130T=	NP_001371055.1:p.Asn710=
NM_001384127.1:c.1719T=	NP_001371056.1:p.Asn573=
NM_001384128.1:c.1719T=	NP_001371057.1:p.Asn573=
NM_001384130.1:c.1440T=	NP_001371059.1:p.Asn480=
NM_001385118.1:c.1719T=	NP_001372047.1:p.Asn573=