Canonical Allele Identifier: CA384372342

Gene: FGD4

Linked Data

• gnomAD v4: 12-32640335-G-C
• MyVariant Identifiers: chr12:g.32793269G>C (hg19) ; chr12:g.32640335G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32640335G>C , CM000674.2:g.32640335G>C	GRCh38
NC_000012.11:g.32793269G>C , CM000674.1:g.32793269G>C	GRCh37
NC_000012.10:g.32684536G>C	NCBI36
NG_008626.2:g.245807G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427716.7:c.2103G>C	ENSP00000394487.2:p.Arg701Ser
ENST00000531134.7:c.2358G>C	ENSP00000431323.1:p.Arg786Ser
ENST00000583694.2:c.2103G>C	ENSP00000462623.2:p.Arg701Ser
ENST00000682739.1:c.1824G>C	ENSP00000507616.1:p.Arg608Ser
ENST00000683182.1:c.915G>C	ENSP00000507831.1:p.Arg305Ser
ENST00000684033.1:n.901G>C
ENST00000525053.6:c.2103G>C	ENSP00000433666.2:p.Arg701Ser
ENST00000531134.6:c.2358G>C	ENSP00000431323.1:p.Arg786Ser
ENST00000534526.7:c.2514G>C MANE Select	ENSP00000449273.1:p.Arg838Ser
ENST00000427716.6:c.2103G>C	ENSP00000394487.2:p.Arg701Ser
ENST00000493087.5:c.*1514G>C	ENSP00000437109.1:n.*1514G>C
ENST00000494977.1:c.1991G>C
ENST00000525053.5:c.2439G>C	ENSP00000433666.1:p.Arg813Ser
ENST00000531134.5:c.2358G>C	ENSP00000431323.1:p.Arg786Ser
ENST00000534526.6:c.2514G>C	ENSP00000449273.1:p.Arg838Ser
ENST00000546442.5:c.1824G>C	ENSP00000446695.1:p.Arg608Ser
ENST00000551984.5:c.*1472G>C	ENSP00000449614.1:n.*1472G>C
NM_001304480.1:c.2439G>C	NP_001291409.1:p.Arg813Ser
NM_001304481.1:c.2358G>C	NP_001291410.1:p.Arg786Ser
NM_001304484.1:c.1071G>C	NP_001291413.1:p.Arg357Ser
NM_139241.3:c.2103G>C	NP_640334.2:p.Arg701Ser
XM_005253304.3:c.2595G>C	XP_005253361.1:p.Arg865Ser
XM_005253307.2:c.1824G>C	XP_005253364.1:p.Arg608Ser
XM_005253308.3:c.1824G>C	XP_005253365.1:p.Arg608Ser
XM_005253309.1:c.1824G>C	XP_005253366.1:p.Arg608Ser
XM_005253310.3:c.1359G>C	XP_005253367.1:p.Arg453Ser
XM_011520554.1:c.2397G>C	XP_011518856.1:p.Arg799Ser
XM_011520555.1:c.2103G>C	XP_011518857.1:p.Arg701Ser
XM_011520556.1:c.2103G>C	XP_011518858.1:p.Arg701Ser
XM_011520557.1:c.1551G>C	XP_011518859.1:p.Arg517Ser
XM_011520558.1:c.1506G>C	XP_011518860.1:p.Arg502Ser
XM_011520559.1:c.1338G>C	XP_011518861.1:p.Arg446Ser
NM_001330373.1:c.1824G>C	NP_001317302.1:p.Arg608Ser
NM_001330374.1:c.1824G>C	NP_001317303.1:p.Arg608Ser
XM_005253304.4:c.2595G>C	XP_005253361.1:p.Arg865Ser
XM_005253308.5:c.1824G>C	XP_005253365.1:p.Arg608Ser
XM_005253310.4:c.1359G>C	XP_005253367.1:p.Arg453Ser
XM_011520558.2:c.1506G>C	XP_011518860.1:p.Arg502Ser
XM_011520559.3:c.1338G>C	XP_011518861.1:p.Arg446Ser
XM_017018803.1:c.2595G>C	XP_016874292.1:p.Arg865Ser
XM_017018805.1:c.1551G>C	XP_016874294.1:p.Arg517Ser
XM_024448837.1:c.1824G>C	XP_024304605.1:p.Arg608Ser
XM_024448838.1:c.1824G>C	XP_024304606.1:p.Arg608Ser
XM_024448839.1:c.1824G>C	XP_024304607.1:p.Arg608Ser
XM_024448840.1:c.1212G>C	XP_024304608.1:p.Arg404Ser
NM_001370297.1:c.1551G>C	NP_001357226.1:p.Arg517Ser
NM_001370298.1:c.2595G>C	NP_001357227.1:p.Arg865Ser
NM_001304484.2:c.1071G>C	NP_001291413.1:p.Arg357Ser
NM_001330373.2:c.1824G>C	NP_001317302.1:p.Arg608Ser
NM_001330374.2:c.1824G>C	NP_001317303.1:p.Arg608Ser
NM_001370298.3:c.2514G>C MANE Select	NP_001357227.2:p.Arg838Ser
NM_001384126.1:c.2514G>C	NP_001371055.1:p.Arg838Ser
NM_001384127.1:c.2103G>C	NP_001371056.1:p.Arg701Ser
NM_001384128.1:c.2103G>C	NP_001371057.1:p.Arg701Ser
NM_001384130.1:c.1824G>C	NP_001371059.1:p.Arg608Ser
NM_001385118.1:c.2103G>C	NP_001372047.1:p.Arg701Ser