Canonical Allele Identifier: CA2618214730

Gene: FGD4

Linked Data

• gnomAD v4: 12-32611322-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32611322A>G , CM000674.2:g.32611322A>G	GRCh38
NC_000012.11:g.32764256A>G , CM000674.1:g.32764256A>G	GRCh37
NC_000012.10:g.32655523A>G	NCBI36
NG_008626.2:g.216794A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427716.7:c.1338+39A>G	ENSP00000394487.2:n.1338+39A>G
ENST00000531134.7:c.1593+39A>G	ENSP00000431323.1:n.1593+39A>G
ENST00000583694.2:c.1338+39A>G	ENSP00000462623.2:n.1338+39A>G
ENST00000682739.1:c.1059+39A>G	ENSP00000507616.1:n.1059+39A>G
ENST00000683182.1:c.150+39A>G	ENSP00000507831.1:n.150+39A>G
ENST00000683515.1:n.845+39A>G
ENST00000525053.6:c.1338+39A>G	ENSP00000433666.2:n.1338+39A>G
ENST00000531134.6:c.1593+39A>G	ENSP00000431323.1:n.1593+39A>G
ENST00000534526.7:c.1749+39A>G MANE Select	ENSP00000449273.1:n.1749+39A>G
ENST00000395740.5:c.*730+39A>G	ENSP00000379089.1:n.*730+39A>G
ENST00000427716.6:c.1338+39A>G	ENSP00000394487.2:n.1338+39A>G
ENST00000493087.5:c.*749+39A>G	ENSP00000437109.1:n.*749+39A>G
ENST00000494977.1:c.927+39A>G
ENST00000525053.5:c.1674+39A>G	ENSP00000433666.1:n.1674+39A>G
ENST00000531134.5:c.1593+39A>G	ENSP00000431323.1:n.1593+39A>G
ENST00000534526.6:c.1749+39A>G	ENSP00000449273.1:n.1749+39A>G
ENST00000546442.5:c.1059+39A>G	ENSP00000446695.1:n.1059+39A>G
ENST00000551984.5:c.*707+39A>G	ENSP00000449614.1:n.*707+39A>G
NM_001304480.1:c.1674+39A>G	NP_001291409.1:n.1674+39A>G
NM_001304481.1:c.1593+39A>G	NP_001291410.1:n.1593+39A>G
NM_001304483.1:c.594+39A>G	NP_001291412.1:n.594+39A>G
NM_001304484.1:c.306+39A>G	NP_001291413.1:n.306+39A>G
NM_139241.3:c.1338+39A>G	NP_640334.2:n.1338+39A>G
XM_005253304.3:c.1830+39A>G	XP_005253361.1:n.1830+39A>G
XM_005253307.2:c.1059+39A>G	XP_005253364.1:n.1059+39A>G
XM_005253308.3:c.1059+39A>G	XP_005253365.1:n.1059+39A>G
XM_005253309.1:c.1059+39A>G	XP_005253366.1:n.1059+39A>G
XM_005253310.3:c.594+39A>G	XP_005253367.1:n.594+39A>G
XM_011520554.1:c.1632+39A>G	XP_011518856.1:n.1632+39A>G
XM_011520555.1:c.1338+39A>G	XP_011518857.1:n.1338+39A>G
XM_011520556.1:c.1338+39A>G	XP_011518858.1:n.1338+39A>G
XM_011520557.1:c.786+39A>G	XP_011518859.1:n.786+39A>G
XM_011520558.1:c.741+39A>G	XP_011518860.1:n.741+39A>G
XM_011520559.1:c.573+39A>G	XP_011518861.1:n.573+39A>G
NM_001330373.1:c.1059+39A>G	NP_001317302.1:n.1059+39A>G
NM_001330374.1:c.1059+39A>G	NP_001317303.1:n.1059+39A>G
XM_005253304.4:c.1830+39A>G	XP_005253361.1:n.1830+39A>G
XM_005253308.5:c.1059+39A>G	XP_005253365.1:n.1059+39A>G
XM_005253310.4:c.594+39A>G	XP_005253367.1:n.594+39A>G
XM_011520558.2:c.741+39A>G	XP_011518860.1:n.741+39A>G
XM_011520559.3:c.573+39A>G	XP_011518861.1:n.573+39A>G
XM_017018803.1:c.1830+39A>G	XP_016874292.1:n.1830+39A>G
XM_017018805.1:c.786+39A>G	XP_016874294.1:n.786+39A>G
XM_024448837.1:c.1059+39A>G	XP_024304605.1:n.1059+39A>G
XM_024448838.1:c.1059+39A>G	XP_024304606.1:n.1059+39A>G
XM_024448839.1:c.1059+39A>G	XP_024304607.1:n.1059+39A>G
XM_024448840.1:c.447+39A>G	XP_024304608.1:n.447+39A>G
NM_001370297.1:c.786+39A>G	NP_001357226.1:n.786+39A>G
NM_001370298.1:c.1830+39A>G	NP_001357227.1:n.1830+39A>G
NM_001304483.2:c.594+39A>G	NP_001291412.1:n.594+39A>G
NM_001304484.2:c.306+39A>G	NP_001291413.1:n.306+39A>G
NM_001330373.2:c.1059+39A>G	NP_001317302.1:n.1059+39A>G
NM_001330374.2:c.1059+39A>G	NP_001317303.1:n.1059+39A>G
NM_001370298.3:c.1749+39A>G MANE Select	NP_001357227.2:n.1749+39A>G
NM_001384126.1:c.1749+39A>G	NP_001371055.1:n.1749+39A>G
NM_001384127.1:c.1338+39A>G	NP_001371056.1:n.1338+39A>G
NM_001384128.1:c.1338+39A>G	NP_001371057.1:n.1338+39A>G
NM_001384130.1:c.1059+39A>G	NP_001371059.1:n.1059+39A>G
NM_001385118.1:c.1338+39A>G	NP_001372047.1:n.1338+39A>G