Canonical Allele Identifier: CA2026251404

Gene: FGD4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32598779T= , CM000674.2:g.32598779T=	GRCh38
NC_000012.11:g.32751713T= , CM000674.1:g.32751713T=	GRCh37
NC_000012.10:g.32642980T=	NCBI36
NG_008626.2:g.204251T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427716.7:c.690+193T=	ENSP00000394487.2:n.690+193T=
ENST00000531134.7:c.945+193T=	ENSP00000431323.1:n.945+193T=
ENST00000583694.2:c.690+193T=	ENSP00000462623.2:n.690+193T=
ENST00000682739.1:c.411+193T=	ENSP00000507616.1:n.411+193T=
ENST00000683182.1:c.-360+193T=	ENSP00000507831.1:n.-360+193T=
ENST00000683515.1:n.197+193T=
ENST00000525053.6:c.690+193T=	ENSP00000433666.2:n.690+193T=
ENST00000531134.6:c.945+193T=	ENSP00000431323.1:n.945+193T=
ENST00000534526.7:c.1101+193T= MANE Select	ENSP00000449273.1:n.1101+193T=
ENST00000395740.5:c.690+193T=	ENSP00000379089.1:n.690+193T=
ENST00000427716.6:c.690+193T=	ENSP00000394487.2:n.690+193T=
ENST00000493087.5:c.690+193T=	ENSP00000437109.1:n.690+193T=
ENST00000494977.1:c.179+193T=
ENST00000525053.5:c.1026+193T=	ENSP00000433666.1:n.1026+193T=
ENST00000531134.5:c.945+193T=	ENSP00000431323.1:n.945+193T=
ENST00000534526.6:c.1101+193T=	ENSP00000449273.1:n.1101+193T=
ENST00000546442.5:c.411+193T=	ENSP00000446695.1:n.411+193T=
ENST00000551984.5:c.*59+193T=	ENSP00000449614.1:n.*59+193T=
NM_001304480.1:c.1026+193T=	NP_001291409.1:n.1026+193T=
NM_001304481.1:c.945+193T=	NP_001291410.1:n.945+193T=
NM_001304483.1:c.-155+193T=	NP_001291412.1:n.-155+193T=
NM_001304484.1:c.-462+193T=	NP_001291413.1:n.-462+193T=
NM_139241.3:c.690+193T=	NP_640334.2:n.690+193T=
XM_005253304.3:c.1182+193T=	XP_005253361.1:n.1182+193T=
XM_005253307.2:c.411+193T=	XP_005253364.1:n.411+193T=
XM_005253308.3:c.411+193T=	XP_005253365.1:n.411+193T=
XM_005253309.1:c.411+193T=	XP_005253366.1:n.411+193T=
XM_011520554.1:c.984+193T=	XP_011518856.1:n.984+193T=
XM_011520555.1:c.690+193T=	XP_011518857.1:n.690+193T=
XM_011520556.1:c.690+193T=	XP_011518858.1:n.690+193T=
XM_011520557.1:c.138+193T=	XP_011518859.1:n.138+193T=
XM_011520558.1:c.93+193T=	XP_011518860.1:n.93+193T=
NM_001330373.1:c.411+193T=	NP_001317302.1:n.411+193T=
NM_001330374.1:c.411+193T=	NP_001317303.1:n.411+193T=
XM_005253304.4:c.1182+193T=	XP_005253361.1:n.1182+193T=
XM_005253308.5:c.411+193T=	XP_005253365.1:n.411+193T=
XM_005253310.4:c.-155+193T=	XP_005253367.1:n.-155+193T=
XM_011520558.2:c.93+193T=	XP_011518860.1:n.93+193T=
XM_017018803.1:c.1182+193T=	XP_016874292.1:n.1182+193T=
XM_017018805.1:c.138+193T=	XP_016874294.1:n.138+193T=
XM_024448837.1:c.411+193T=	XP_024304605.1:n.411+193T=
XM_024448838.1:c.411+193T=	XP_024304606.1:n.411+193T=
XM_024448839.1:c.411+193T=	XP_024304607.1:n.411+193T=
XM_024448840.1:c.-113+193T=	XP_024304608.1:n.-113+193T=
XR_001748576.1:n.1372+193T=
NM_001370297.1:c.138+193T=	NP_001357226.1:n.138+193T=
NM_001370298.1:c.1182+193T=	NP_001357227.1:n.1182+193T=
NM_001304483.2:c.-155+193T=	NP_001291412.1:n.-155+193T=
NM_001304484.2:c.-462+193T=	NP_001291413.1:n.-462+193T=
NM_001330373.2:c.411+193T=	NP_001317302.1:n.411+193T=
NM_001330374.2:c.411+193T=	NP_001317303.1:n.411+193T=
NM_001370298.3:c.1101+193T= MANE Select	NP_001357227.2:n.1101+193T=
NM_001384126.1:c.1101+193T=	NP_001371055.1:n.1101+193T=
NM_001384127.1:c.690+193T=	NP_001371056.1:n.690+193T=
NM_001384128.1:c.690+193T=	NP_001371057.1:n.690+193T=
NM_001384130.1:c.411+193T=	NP_001371059.1:n.411+193T=
NM_001385118.1:c.690+193T=	NP_001372047.1:n.690+193T=