Canonical Allele Identifier: CA384361044

Gene: FGD4

Linked Data

• ClinVar Variation Id: 2141629
• ClinVar RCV Id: RCV003074001
• dbSNP Id: rs1208112274
• MyVariant Identifiers: chr12:g.32764118A>C (hg19) ; chr12:g.32611184A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32611184A>C , CM000674.2:g.32611184A>C	GRCh38
NC_000012.11:g.32764118A>C , CM000674.1:g.32764118A>C	GRCh37
NC_000012.10:g.32655385A>C	NCBI36
NG_008626.2:g.216656A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427716.7:c.1239A>C	ENSP00000394487.2:p.Glu413Asp
ENST00000531134.7:c.1494A>C	ENSP00000431323.1:p.Glu498Asp
ENST00000583694.2:c.1239A>C	ENSP00000462623.2:p.Glu413Asp
ENST00000682739.1:c.960A>C	ENSP00000507616.1:p.Glu320Asp
ENST00000683182.1:c.51A>C	ENSP00000507831.1:p.Glu17Asp
ENST00000683515.1:n.746A>C
ENST00000525053.6:c.1239A>C	ENSP00000433666.2:p.Glu413Asp
ENST00000531134.6:c.1494A>C	ENSP00000431323.1:p.Glu498Asp
ENST00000534526.7:c.1650A>C MANE Select	ENSP00000449273.1:p.Glu550Asp
ENST00000395740.5:c.*631A>C	ENSP00000379089.1:n.*631A>C
ENST00000427716.6:c.1239A>C	ENSP00000394487.2:p.Glu413Asp
ENST00000493087.5:c.*650A>C	ENSP00000437109.1:n.*650A>C
ENST00000494977.1:c.828A>C
ENST00000525053.5:c.1575A>C	ENSP00000433666.1:p.Glu525Asp
ENST00000531134.5:c.1494A>C	ENSP00000431323.1:p.Glu498Asp
ENST00000534526.6:c.1650A>C	ENSP00000449273.1:p.Glu550Asp
ENST00000546442.5:c.960A>C	ENSP00000446695.1:p.Glu320Asp
ENST00000551984.5:c.*608A>C	ENSP00000449614.1:n.*608A>C
NM_001304480.1:c.1575A>C	NP_001291409.1:p.Glu525Asp
NM_001304481.1:c.1494A>C	NP_001291410.1:p.Glu498Asp
NM_001304483.1:c.495A>C	NP_001291412.1:p.Glu165Asp
NM_001304484.1:c.207A>C	NP_001291413.1:p.Glu69Asp
NM_139241.3:c.1239A>C	NP_640334.2:p.Glu413Asp
XM_005253304.3:c.1731A>C	XP_005253361.1:p.Glu577Asp
XM_005253307.2:c.960A>C	XP_005253364.1:p.Glu320Asp
XM_005253308.3:c.960A>C	XP_005253365.1:p.Glu320Asp
XM_005253309.1:c.960A>C	XP_005253366.1:p.Glu320Asp
XM_005253310.3:c.495A>C	XP_005253367.1:p.Glu165Asp
XM_011520554.1:c.1533A>C	XP_011518856.1:p.Glu511Asp
XM_011520555.1:c.1239A>C	XP_011518857.1:p.Glu413Asp
XM_011520556.1:c.1239A>C	XP_011518858.1:p.Glu413Asp
XM_011520557.1:c.687A>C	XP_011518859.1:p.Glu229Asp
XM_011520558.1:c.642A>C	XP_011518860.1:p.Glu214Asp
XM_011520559.1:c.474A>C	XP_011518861.1:p.Glu158Asp
NM_001330373.1:c.960A>C	NP_001317302.1:p.Glu320Asp
NM_001330374.1:c.960A>C	NP_001317303.1:p.Glu320Asp
XM_005253304.4:c.1731A>C	XP_005253361.1:p.Glu577Asp
XM_005253308.5:c.960A>C	XP_005253365.1:p.Glu320Asp
XM_005253310.4:c.495A>C	XP_005253367.1:p.Glu165Asp
XM_011520558.2:c.642A>C	XP_011518860.1:p.Glu214Asp
XM_011520559.3:c.474A>C	XP_011518861.1:p.Glu158Asp
XM_017018803.1:c.1731A>C	XP_016874292.1:p.Glu577Asp
XM_017018805.1:c.687A>C	XP_016874294.1:p.Glu229Asp
XM_024448837.1:c.960A>C	XP_024304605.1:p.Glu320Asp
XM_024448838.1:c.960A>C	XP_024304606.1:p.Glu320Asp
XM_024448839.1:c.960A>C	XP_024304607.1:p.Glu320Asp
XM_024448840.1:c.348A>C	XP_024304608.1:p.Glu116Asp
XR_001748576.1:n.1940A>C
NM_001370297.1:c.687A>C	NP_001357226.1:p.Glu229Asp
NM_001370298.1:c.1731A>C	NP_001357227.1:p.Glu577Asp
NM_001304483.2:c.495A>C	NP_001291412.1:p.Glu165Asp
NM_001304484.2:c.207A>C	NP_001291413.1:p.Glu69Asp
NM_001330373.2:c.960A>C	NP_001317302.1:p.Glu320Asp
NM_001330374.2:c.960A>C	NP_001317303.1:p.Glu320Asp
NM_001370298.3:c.1650A>C MANE Select	NP_001357227.2:p.Glu550Asp
NM_001384126.1:c.1650A>C	NP_001371055.1:p.Glu550Asp
NM_001384127.1:c.1239A>C	NP_001371056.1:p.Glu413Asp
NM_001384128.1:c.1239A>C	NP_001371057.1:p.Glu413Asp
NM_001384130.1:c.960A>C	NP_001371059.1:p.Glu320Asp
NM_001385118.1:c.1239A>C	NP_001372047.1:p.Glu413Asp