Canonical Allele Identifier: CA384372362

Gene: FGD4

Linked Data

• MyVariant Identifiers: chr12:g.32793278C>G (hg19) ; chr12:g.32640344C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32640344C>G , CM000674.2:g.32640344C>G	GRCh38
NC_000012.11:g.32793278C>G , CM000674.1:g.32793278C>G	GRCh37
NC_000012.10:g.32684545C>G	NCBI36
NG_008626.2:g.245816C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427716.7:c.2112C>G	ENSP00000394487.2:p.Asp704Glu
ENST00000531134.7:c.2367C>G	ENSP00000431323.1:p.Asp789Glu
ENST00000583694.2:c.2112C>G	ENSP00000462623.2:p.Asp704Glu
ENST00000682739.1:c.1833C>G	ENSP00000507616.1:p.Asp611Glu
ENST00000683182.1:c.924C>G	ENSP00000507831.1:p.Asp308Glu
ENST00000684033.1:n.910C>G
ENST00000525053.6:c.2112C>G	ENSP00000433666.2:p.Asp704Glu
ENST00000531134.6:c.2367C>G	ENSP00000431323.1:p.Asp789Glu
ENST00000534526.7:c.2523C>G MANE Select	ENSP00000449273.1:p.Asp841Glu
ENST00000427716.6:c.2112C>G	ENSP00000394487.2:p.Asp704Glu
ENST00000493087.5:c.*1523C>G	ENSP00000437109.1:n.*1523C>G
ENST00000494977.1:c.2000C>G
ENST00000525053.5:c.2448C>G	ENSP00000433666.1:p.Asp816Glu
ENST00000531134.5:c.2367C>G	ENSP00000431323.1:p.Asp789Glu
ENST00000534526.6:c.2523C>G	ENSP00000449273.1:p.Asp841Glu
ENST00000546442.5:c.1833C>G	ENSP00000446695.1:p.Asp611Glu
ENST00000551984.5:c.*1481C>G	ENSP00000449614.1:n.*1481C>G
NM_001304480.1:c.2448C>G	NP_001291409.1:p.Asp816Glu
NM_001304481.1:c.2367C>G	NP_001291410.1:p.Asp789Glu
NM_001304484.1:c.1080C>G	NP_001291413.1:p.Asp360Glu
NM_139241.3:c.2112C>G	NP_640334.2:p.Asp704Glu
XM_005253304.3:c.2604C>G	XP_005253361.1:p.Asp868Glu
XM_005253307.2:c.1833C>G	XP_005253364.1:p.Asp611Glu
XM_005253308.3:c.1833C>G	XP_005253365.1:p.Asp611Glu
XM_005253309.1:c.1833C>G	XP_005253366.1:p.Asp611Glu
XM_005253310.3:c.1368C>G	XP_005253367.1:p.Asp456Glu
XM_011520554.1:c.2406C>G	XP_011518856.1:p.Asp802Glu
XM_011520555.1:c.2112C>G	XP_011518857.1:p.Asp704Glu
XM_011520556.1:c.2112C>G	XP_011518858.1:p.Asp704Glu
XM_011520557.1:c.1560C>G	XP_011518859.1:p.Asp520Glu
XM_011520558.1:c.1515C>G	XP_011518860.1:p.Asp505Glu
XM_011520559.1:c.1347C>G	XP_011518861.1:p.Asp449Glu
NM_001330373.1:c.1833C>G	NP_001317302.1:p.Asp611Glu
NM_001330374.1:c.1833C>G	NP_001317303.1:p.Asp611Glu
XM_005253304.4:c.2604C>G	XP_005253361.1:p.Asp868Glu
XM_005253308.5:c.1833C>G	XP_005253365.1:p.Asp611Glu
XM_005253310.4:c.1368C>G	XP_005253367.1:p.Asp456Glu
XM_011520558.2:c.1515C>G	XP_011518860.1:p.Asp505Glu
XM_011520559.3:c.1347C>G	XP_011518861.1:p.Asp449Glu
XM_017018803.1:c.2604C>G	XP_016874292.1:p.Asp868Glu
XM_017018805.1:c.1560C>G	XP_016874294.1:p.Asp520Glu
XM_024448837.1:c.1833C>G	XP_024304605.1:p.Asp611Glu
XM_024448838.1:c.1833C>G	XP_024304606.1:p.Asp611Glu
XM_024448839.1:c.1833C>G	XP_024304607.1:p.Asp611Glu
XM_024448840.1:c.1221C>G	XP_024304608.1:p.Asp407Glu
NM_001370297.1:c.1560C>G	NP_001357226.1:p.Asp520Glu
NM_001370298.1:c.2604C>G	NP_001357227.1:p.Asp868Glu
NM_001304484.2:c.1080C>G	NP_001291413.1:p.Asp360Glu
NM_001330373.2:c.1833C>G	NP_001317302.1:p.Asp611Glu
NM_001330374.2:c.1833C>G	NP_001317303.1:p.Asp611Glu
NM_001370298.3:c.2523C>G MANE Select	NP_001357227.2:p.Asp841Glu
NM_001384126.1:c.2523C>G	NP_001371055.1:p.Asp841Glu
NM_001384127.1:c.2112C>G	NP_001371056.1:p.Asp704Glu
NM_001384128.1:c.2112C>G	NP_001371057.1:p.Asp704Glu
NM_001384130.1:c.1833C>G	NP_001371059.1:p.Asp611Glu
NM_001385118.1:c.2112C>G	NP_001372047.1:p.Asp704Glu