Canonical Allele Identifier: CA479388335

Gene: FGD4

Linked Data

• ClinVar Variation Id: 1547688
• ClinVar RCV Id: RCV002165638
• dbSNP Id: rs2136433041
• MyVariant Identifiers: chr12:g.32735086A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32582152A>C , CM000674.2:g.32582152A>C	GRCh38
NC_000012.11:g.32735086A>C , CM000674.1:g.32735086A>C	GRCh37
NC_000012.10:g.32626353A>C	NCBI36
NG_008626.2:g.187624A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427716.7:c.285A>C	ENSP00000394487.2:p.Ala95=
ENST00000531134.7:c.540A>C	ENSP00000431323.1:p.Ala180=
ENST00000583694.2:c.285A>C	ENSP00000462623.2:p.Ala95=
ENST00000682739.1:c.6A>C	ENSP00000507616.1:p.Ala2=
ENST00000683182.1:c.-449-16345A>C	ENSP00000507831.1:n.-449-16345A>C
ENST00000525053.6:c.285A>C	ENSP00000433666.2:p.Ala95=
ENST00000531134.6:c.540A>C	ENSP00000431323.1:p.Ala180=
ENST00000534526.7:c.696A>C MANE Select	ENSP00000449273.1:p.Ala232=
ENST00000395740.5:c.285A>C	ENSP00000379089.1:p.Ala95=
ENST00000427716.6:c.285A>C	ENSP00000394487.2:p.Ala95=
ENST00000472289.5:c.285A>C	ENSP00000434356.1:p.Ala95=
ENST00000493087.5:c.285A>C	ENSP00000437109.1:p.Ala95=
ENST00000494275.5:n.636A>C
ENST00000525053.5:c.621A>C	ENSP00000433666.1:p.Ala207=
ENST00000531134.5:c.540A>C	ENSP00000431323.1:p.Ala180=
ENST00000534526.6:c.696A>C	ENSP00000449273.1:p.Ala232=
ENST00000546442.5:c.6A>C	ENSP00000446695.1:p.Ala2=
ENST00000550091.5:n.450A>C
ENST00000551984.5:c.92+5703A>C	ENSP00000449614.1:n.92+5703A>C
NM_001304480.1:c.621A>C	NP_001291409.1:p.Ala207=
NM_001304481.1:c.540A>C	NP_001291410.1:p.Ala180=
NM_001304483.1:c.-560A>C	NP_001291412.1:n.-560A>C
NM_001304484.1:c.-867A>C	NP_001291413.1:n.-867A>C
NM_139241.3:c.285A>C	NP_640334.2:p.Ala95=
XM_005253304.3:c.777A>C	XP_005253361.1:p.Ala259=
XM_005253307.2:c.6A>C	XP_005253364.1:p.Ala2=
XM_005253308.3:c.6A>C	XP_005253365.1:p.Ala2=
XM_005253309.1:c.6A>C	XP_005253366.1:p.Ala2=
XM_011520554.1:c.579A>C	XP_011518856.1:p.Ala193=
XM_011520555.1:c.285A>C	XP_011518857.1:p.Ala95=
XM_011520556.1:c.285A>C	XP_011518858.1:p.Ala95=
XM_011520557.1:c.49-16345A>C	XP_011518859.1:n.49-16345A>C
NM_001330373.1:c.6A>C	NP_001317302.1:p.Ala2=
NM_001330374.1:c.6A>C	NP_001317303.1:p.Ala2=
XM_005253304.4:c.777A>C	XP_005253361.1:p.Ala259=
XM_005253308.5:c.6A>C	XP_005253365.1:p.Ala2=
XM_005253310.4:c.-560A>C	XP_005253367.1:n.-560A>C
XM_017018803.1:c.777A>C	XP_016874292.1:p.Ala259=
XM_017018805.1:c.49-16345A>C	XP_016874294.1:n.49-16345A>C
XM_024448837.1:c.6A>C	XP_024304605.1:p.Ala2=
XM_024448838.1:c.6A>C	XP_024304606.1:p.Ala2=
XM_024448839.1:c.6A>C	XP_024304607.1:p.Ala2=
XM_024448840.1:c.-202-16345A>C	XP_024304608.1:n.-202-16345A>C
XR_001748576.1:n.967A>C
NM_001370297.1:c.49-16345A>C	NP_001357226.1:n.49-16345A>C
NM_001370298.1:c.777A>C	NP_001357227.1:p.Ala259=
NM_001304483.2:c.-560A>C	NP_001291412.1:n.-560A>C
NM_001304484.2:c.-867A>C	NP_001291413.1:n.-867A>C
NM_001330373.2:c.6A>C	NP_001317302.1:p.Ala2=
NM_001330374.2:c.6A>C	NP_001317303.1:p.Ala2=
NM_001370298.3:c.696A>C MANE Select	NP_001357227.2:p.Ala232=
NM_001384126.1:c.696A>C	NP_001371055.1:p.Ala232=
NM_001384127.1:c.285A>C	NP_001371056.1:p.Ala95=
NM_001384128.1:c.285A>C	NP_001371057.1:p.Ala95=
NM_001384130.1:c.6A>C	NP_001371059.1:p.Ala2=
NM_001384131.1:c.285A>C	NP_001371060.1:p.Ala95=
NM_001384132.1:c.285A>C	NP_001371061.1:p.Ala95=
NM_001385118.1:c.285A>C	NP_001372047.1:p.Ala95=
NR_168884.1:n.522A>C