Canonical Allele Identifier: CA479169302
Gene: FGD4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.32778665T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32625731T>G , CM000674.2:g.32625731T>G GRCh38
NC_000012.11:g.32778665T>G , CM000674.1:g.32778665T>G GRCh37
NC_000012.10:g.32669932T>G NCBI36
NG_008626.2:g.231203T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000427716.7:c.1713T>G ENSP00000394487.2:p.Pro571=
ENST00000531134.7:c.1968T>G ENSP00000431323.1:p.Pro656=
ENST00000583694.2:c.1713T>G ENSP00000462623.2:p.Pro571=
ENST00000682739.1:c.1434T>G ENSP00000507616.1:p.Pro478=
ENST00000683182.1:c.525T>G ENSP00000507831.1:p.Pro175=
ENST00000683515.1:n.1220T>G
ENST00000684033.1:n.511T>G
ENST00000525053.6:c.1713T>G ENSP00000433666.2:p.Pro571=
ENST00000531134.6:c.1968T>G ENSP00000431323.1:p.Pro656=
ENST00000534526.7:c.2124T>G MANE Select ENSP00000449273.1:p.Pro708=
ENST00000395740.5:c.*1105T>G ENSP00000379089.1:n.*1105T>G
ENST00000427716.6:c.1713T>G ENSP00000394487.2:p.Pro571=
ENST00000493087.5:c.*1124T>G ENSP00000437109.1:n.*1124T>G
ENST00000494977.1:c.1395T>G
ENST00000525053.5:c.2049T>G ENSP00000433666.1:p.Pro683=
ENST00000531134.5:c.1968T>G ENSP00000431323.1:p.Pro656=
ENST00000534526.6:c.2124T>G ENSP00000449273.1:p.Pro708=
ENST00000546442.5:c.1434T>G ENSP00000446695.1:p.Pro478=
ENST00000551984.5:c.*1082T>G ENSP00000449614.1:n.*1082T>G
NM_001304480.1:c.2049T>G NP_001291409.1:p.Pro683=
NM_001304481.1:c.1968T>G NP_001291410.1:p.Pro656=
NM_001304483.1:c.969T>G NP_001291412.1:p.Pro323=
NM_001304484.1:c.681T>G NP_001291413.1:p.Pro227=
NM_139241.3:c.1713T>G NP_640334.2:p.Pro571=
XM_005253304.3:c.2205T>G XP_005253361.1:p.Pro735=
XM_005253307.2:c.1434T>G XP_005253364.1:p.Pro478=
XM_005253308.3:c.1434T>G XP_005253365.1:p.Pro478=
XM_005253309.1:c.1434T>G XP_005253366.1:p.Pro478=
XM_005253310.3:c.969T>G XP_005253367.1:p.Pro323=
XM_011520554.1:c.2007T>G XP_011518856.1:p.Pro669=
XM_011520555.1:c.1713T>G XP_011518857.1:p.Pro571=
XM_011520556.1:c.1713T>G XP_011518858.1:p.Pro571=
XM_011520557.1:c.1161T>G XP_011518859.1:p.Pro387=
XM_011520558.1:c.1116T>G XP_011518860.1:p.Pro372=
XM_011520559.1:c.948T>G XP_011518861.1:p.Pro316=
NM_001330373.1:c.1434T>G NP_001317302.1:p.Pro478=
NM_001330374.1:c.1434T>G NP_001317303.1:p.Pro478=
XM_005253304.4:c.2205T>G XP_005253361.1:p.Pro735=
XM_005253308.5:c.1434T>G XP_005253365.1:p.Pro478=
XM_005253310.4:c.969T>G XP_005253367.1:p.Pro323=
XM_011520558.2:c.1116T>G XP_011518860.1:p.Pro372=
XM_011520559.3:c.948T>G XP_011518861.1:p.Pro316=
XM_017018803.1:c.2205T>G XP_016874292.1:p.Pro735=
XM_017018805.1:c.1161T>G XP_016874294.1:p.Pro387=
XM_024448837.1:c.1434T>G XP_024304605.1:p.Pro478=
XM_024448838.1:c.1434T>G XP_024304606.1:p.Pro478=
XM_024448839.1:c.1434T>G XP_024304607.1:p.Pro478=
XM_024448840.1:c.822T>G XP_024304608.1:p.Pro274=
NM_001370297.1:c.1161T>G NP_001357226.1:p.Pro387=
NM_001370298.1:c.2205T>G NP_001357227.1:p.Pro735=
NM_001304483.2:c.969T>G NP_001291412.1:p.Pro323=
NM_001304484.2:c.681T>G NP_001291413.1:p.Pro227=
NM_001330373.2:c.1434T>G NP_001317302.1:p.Pro478=
NM_001330374.2:c.1434T>G NP_001317303.1:p.Pro478=
NM_001370298.3:c.2124T>G MANE Select NP_001357227.2:p.Pro708=
NM_001384126.1:c.2124T>G NP_001371055.1:p.Pro708=
NM_001384127.1:c.1713T>G NP_001371056.1:p.Pro571=
NM_001384128.1:c.1713T>G NP_001371057.1:p.Pro571=
NM_001384130.1:c.1434T>G NP_001371059.1:p.Pro478=
NM_001385118.1:c.1713T>G NP_001372047.1:p.Pro571=