Canonical Allele Identifier: CA479388523
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 543495
ClinVar RCV Id: RCV000654269

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32582284T>A , CM000674.2:g.32582284T>A GRCh38
NC_000012.11:g.32735218T>A , CM000674.1:g.32735218T>A GRCh37
NC_000012.10:g.32626485T>A NCBI36
NG_008626.2:g.187756T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000525053.6:c.417T>A ENSP00000433666.2:p.Pro139=
ENST00000531134.6:c.672T>A ENSP00000431323.1:p.Pro224=
ENST00000534526.7:c.828T>A MANE Select ENSP00000449273.1:p.Pro276=
ENST00000395740.5:c.417T>A ENSP00000379089.1:p.Pro139=
ENST00000427716.6:c.417T>A ENSP00000394487.2:p.Pro139=
ENST00000472289.5:c.417T>A ENSP00000434356.1:p.Pro139=
ENST00000493087.5:c.417T>A ENSP00000437109.1:p.Pro139=
ENST00000494275.5:n.768T>A
ENST00000525053.5:c.753T>A ENSP00000433666.1:p.Pro251=
ENST00000531134.5:c.672T>A ENSP00000431323.1:p.Pro224=
ENST00000534526.6:c.828T>A ENSP00000449273.1:p.Pro276=
ENST00000546442.5:c.138T>A ENSP00000446695.1:p.Pro46=
ENST00000551984.5:c.92+5835T>A ENSP00000449614.1:p.=
NM_001304480.1:c.753T>A NP_001291409.1:p.Pro251=
NM_001304481.1:c.672T>A NP_001291410.1:p.Pro224=
NM_001304483.1:c.-428T>A NP_001291412.1:p.=
NM_001304484.1:c.-735T>A NP_001291413.1:p.=
NM_139241.3:c.417T>A NP_640334.2:p.Pro139=
XM_005253304.3:c.909T>A XP_005253361.1:p.Pro303=
XM_005253307.2:c.138T>A XP_005253364.1:p.Pro46=
XM_005253308.3:c.138T>A XP_005253365.1:p.Pro46=
XM_005253309.1:c.138T>A XP_005253366.1:p.Pro46=
XM_011520554.1:c.711T>A XP_011518856.1:p.Pro237=
XM_011520555.1:c.417T>A XP_011518857.1:p.Pro139=
XM_011520556.1:c.417T>A XP_011518858.1:p.Pro139=
XM_011520557.1:c.49-16213T>A XP_011518859.1:p.=
NM_001330373.1:c.138T>A NP_001317302.1:p.Pro46=
NM_001330374.1:c.138T>A NP_001317303.1:p.Pro46=
XM_005253304.4:c.909T>A XP_005253361.1:p.Pro303=
XM_005253308.5:c.138T>A XP_005253365.1:p.Pro46=
XM_005253310.4:c.-428T>A XP_005253367.1:p.=
XM_017018803.1:c.909T>A XP_016874292.1:p.Pro303=
XM_017018805.1:c.49-16213T>A XP_016874294.1:p.=
XM_024448837.1:c.138T>A XP_024304605.1:p.Pro46=
XM_024448838.1:c.138T>A XP_024304606.1:p.Pro46=
XM_024448839.1:c.138T>A XP_024304607.1:p.Pro46=
XM_024448840.1:c.-202-16213T>A XP_024304608.1:p.=
XR_001748576.1:n.1099T>A
NM_001370297.1:c.49-16213T>A NP_001357226.1:p.=
NM_001370298.1:c.909T>A NP_001357227.1:p.Pro303=
NM_001304483.2:c.-428T>A NP_001291412.1:p.=
NM_001304484.2:c.-735T>A NP_001291413.1:p.=
NM_001330373.2:c.138T>A NP_001317302.1:p.Pro46=
NM_001330374.2:c.138T>A NP_001317303.1:p.Pro46=
NM_001370298.3:c.828T>A MANE Select NP_001357227.2:p.Pro276=
NM_001384126.1:c.828T>A NP_001371055.1:p.Pro276=
NM_001384127.1:c.417T>A NP_001371056.1:p.Pro139=
NM_001384128.1:c.417T>A NP_001371057.1:p.Pro139=
NM_001384130.1:c.138T>A NP_001371059.1:p.Pro46=
NM_001384131.1:c.417T>A NP_001371060.1:p.Pro139=
NM_001384132.1:c.417T>A NP_001371061.1:p.Pro139=
NM_001385118.1:c.417T>A NP_001372047.1:p.Pro139=
NR_168884.1:n.654T>A