Canonical Allele Identifier: CA2618193014

Gene: FGD4

Linked Data

• gnomAD v4: 12-32640239-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32640239C>T , CM000674.2:g.32640239C>T	GRCh38
NC_000012.11:g.32793173C>T , CM000674.1:g.32793173C>T	GRCh37
NC_000012.10:g.32684440C>T	NCBI36
NG_008626.2:g.245711C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427716.7:c.2044-37C>T	ENSP00000394487.2:n.2044-37C>T
ENST00000531134.7:c.2299-37C>T	ENSP00000431323.1:n.2299-37C>T
ENST00000583694.2:c.2044-37C>T	ENSP00000462623.2:n.2044-37C>T
ENST00000682739.1:c.1765-37C>T	ENSP00000507616.1:n.1765-37C>T
ENST00000683182.1:c.856-37C>T	ENSP00000507831.1:n.856-37C>T
ENST00000684033.1:n.842-37C>T
ENST00000525053.6:c.2044-37C>T	ENSP00000433666.2:n.2044-37C>T
ENST00000531134.6:c.2299-37C>T	ENSP00000431323.1:n.2299-37C>T
ENST00000534526.7:c.2455-37C>T MANE Select	ENSP00000449273.1:n.2455-37C>T
ENST00000427716.6:c.2044-37C>T	ENSP00000394487.2:n.2044-37C>T
ENST00000493087.5:c.*1455-37C>T	ENSP00000437109.1:n.*1455-37C>T
ENST00000494977.1:c.1932-37C>T
ENST00000525053.5:c.2380-37C>T	ENSP00000433666.1:n.2380-37C>T
ENST00000531134.5:c.2299-37C>T	ENSP00000431323.1:n.2299-37C>T
ENST00000534526.6:c.2455-37C>T	ENSP00000449273.1:n.2455-37C>T
ENST00000546442.5:c.1765-37C>T	ENSP00000446695.1:n.1765-37C>T
ENST00000551984.5:c.*1413-37C>T	ENSP00000449614.1:n.*1413-37C>T
NM_001304480.1:c.2380-37C>T	NP_001291409.1:n.2380-37C>T
NM_001304481.1:c.2299-37C>T	NP_001291410.1:n.2299-37C>T
NM_001304484.1:c.1012-37C>T	NP_001291413.1:n.1012-37C>T
NM_139241.3:c.2044-37C>T	NP_640334.2:n.2044-37C>T
XM_005253304.3:c.2536-37C>T	XP_005253361.1:n.2536-37C>T
XM_005253307.2:c.1765-37C>T	XP_005253364.1:n.1765-37C>T
XM_005253308.3:c.1765-37C>T	XP_005253365.1:n.1765-37C>T
XM_005253309.1:c.1765-37C>T	XP_005253366.1:n.1765-37C>T
XM_005253310.3:c.1300-37C>T	XP_005253367.1:n.1300-37C>T
XM_011520554.1:c.2338-37C>T	XP_011518856.1:n.2338-37C>T
XM_011520555.1:c.2044-37C>T	XP_011518857.1:n.2044-37C>T
XM_011520556.1:c.2044-37C>T	XP_011518858.1:n.2044-37C>T
XM_011520557.1:c.1492-37C>T	XP_011518859.1:n.1492-37C>T
XM_011520558.1:c.1447-37C>T	XP_011518860.1:n.1447-37C>T
XM_011520559.1:c.1279-37C>T	XP_011518861.1:n.1279-37C>T
NM_001330373.1:c.1765-37C>T	NP_001317302.1:n.1765-37C>T
NM_001330374.1:c.1765-37C>T	NP_001317303.1:n.1765-37C>T
XM_005253304.4:c.2536-37C>T	XP_005253361.1:n.2536-37C>T
XM_005253308.5:c.1765-37C>T	XP_005253365.1:n.1765-37C>T
XM_005253310.4:c.1300-37C>T	XP_005253367.1:n.1300-37C>T
XM_011520558.2:c.1447-37C>T	XP_011518860.1:n.1447-37C>T
XM_011520559.3:c.1279-37C>T	XP_011518861.1:n.1279-37C>T
XM_017018803.1:c.2536-37C>T	XP_016874292.1:n.2536-37C>T
XM_017018805.1:c.1492-37C>T	XP_016874294.1:n.1492-37C>T
XM_024448837.1:c.1765-37C>T	XP_024304605.1:n.1765-37C>T
XM_024448838.1:c.1765-37C>T	XP_024304606.1:n.1765-37C>T
XM_024448839.1:c.1765-37C>T	XP_024304607.1:n.1765-37C>T
XM_024448840.1:c.1153-37C>T	XP_024304608.1:n.1153-37C>T
NM_001370297.1:c.1492-37C>T	NP_001357226.1:n.1492-37C>T
NM_001370298.1:c.2536-37C>T	NP_001357227.1:n.2536-37C>T
NM_001304484.2:c.1012-37C>T	NP_001291413.1:n.1012-37C>T
NM_001330373.2:c.1765-37C>T	NP_001317302.1:n.1765-37C>T
NM_001330374.2:c.1765-37C>T	NP_001317303.1:n.1765-37C>T
NM_001370298.3:c.2455-37C>T MANE Select	NP_001357227.2:n.2455-37C>T
NM_001384126.1:c.2455-37C>T	NP_001371055.1:n.2455-37C>T
NM_001384127.1:c.2044-37C>T	NP_001371056.1:n.2044-37C>T
NM_001384128.1:c.2044-37C>T	NP_001371057.1:n.2044-37C>T
NM_001384130.1:c.1765-37C>T	NP_001371059.1:n.1765-37C>T
NM_001385118.1:c.2044-37C>T	NP_001372047.1:n.2044-37C>T