Canonical Allele Identifier: CA515466126

Gene: OFD1

Linked Data

• gnomAD v4: X-13758384-T-C
• MyVariant Identifiers: chrX:g.13776503T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.13758384T>C , CM000685.2:g.13758384T>C	GRCh38
NC_000023.10:g.13776503T>C , CM000685.1:g.13776503T>C	GRCh37
NC_000023.9:g.13686424T>C	NCBI36
NG_008872.1:g.28672T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380567.6:c.*1283T>C	ENSP00000369941.2:n.*1283T>C
ENST00000398395.8:c.*1115+594T>C	ENSP00000381432.5:n.*1115+594T>C
ENST00000464463.6:n.1753T>C
ENST00000490265.6:n.2119T>C
ENST00000682237.1:c.*1150T>C	ENSP00000507121.1:n.*1150T>C
ENST00000682562.1:c.*2992T>C	ENSP00000507874.1:n.*2992T>C
ENST00000682953.1:c.*2317T>C	ENSP00000507878.1:n.*2317T>C
ENST00000683055.1:c.*905T>C	ENSP00000508191.1:n.*905T>C
ENST00000683284.1:c.*1821T>C	ENSP00000507837.1:n.*1821T>C
ENST00000683427.1:c.*311+594T>C	ENSP00000507290.1:n.*311+594T>C
ENST00000683454.1:n.1604T>C
ENST00000683637.1:n.2699T>C
ENST00000683655.1:c.*1804T>C	ENSP00000506770.1:n.*1804T>C
ENST00000683713.1:c.*1821T>C	ENSP00000507797.1:n.*1821T>C
ENST00000684577.1:c.*1287T>C	ENSP00000507871.1:n.*1287T>C
ENST00000340096.11:c.1590T>C MANE Select	ENSP00000344314.6:p.Ala530=
ENST00000340096.10:c.1590T>C	ENSP00000344314.6:p.Ala530=
ENST00000380550.6:c.1470T>C	ENSP00000369923.3:p.Ala490=
ENST00000380567.5:c.1170T>C	ENSP00000369941.1:p.Ala390=
ENST00000398395.7:c.1011+594T>C	ENSP00000381432.4:n.1011+594T>C
ENST00000490265.5:n.2565T>C
NM_003611.2:c.1590T>C	NP_003602.1:p.Ala530=
XM_005274599.2:c.1611T>C	XP_005274656.1:p.Ala537=
XM_005274602.2:c.1611T>C	XP_005274659.1:p.Ala537=
XM_005274603.2:c.1491T>C	XP_005274660.1:p.Ala497=
XM_005274604.2:c.1470T>C	XP_005274661.1:p.Ala490=
XM_005274606.2:c.1446T>C	XP_005274663.1:p.Ala482=
XM_005274607.3:c.1170T>C	XP_005274664.1:p.Ala390=
XM_011545591.1:c.1611T>C	XP_011543893.1:p.Ala537=
XM_011545592.1:c.1398T>C	XP_011543894.1:p.Ala466=
XM_011545593.1:c.1611T>C	XP_011543895.1:p.Ala537=
XM_011545594.1:c.1269T>C	XP_011543896.1:p.Ala423=
XM_011545595.1:c.1269T>C	XP_011543897.1:p.Ala423=
XM_011545596.1:c.1611T>C	XP_011543898.1:p.Ala537=
XM_011545597.1:c.1170T>C	XP_011543899.1:p.Ala390=
XM_011545598.1:c.315T>C	XP_011543900.1:p.Ala105=
XR_247288.2:n.1950T>C
NM_001330209.1:c.1470T>C	NP_001317138.1:p.Ala490=
NM_001330210.1:c.1170T>C	NP_001317139.1:p.Ala390=
XM_005274606.4:c.1446T>C	XP_005274663.1:p.Ala482=
XM_011545592.3:c.1398T>C	XP_011543894.1:p.Ala466=
XM_011545594.3:c.1269T>C	XP_011543896.1:p.Ala423=
XM_011545597.2:c.1170T>C	XP_011543899.1:p.Ala390=
XM_017029909.1:c.1170T>C	XP_016885398.1:p.Ala390=
XM_017029911.1:c.648T>C	XP_016885400.1:p.Ala216=
XM_024452468.1:c.315T>C	XP_024308236.1:p.Ala105=
XM_024452469.1:c.315T>C	XP_024308237.1:p.Ala105=
XM_024452470.1:c.315T>C	XP_024308238.1:p.Ala105=
XM_024452471.1:c.315T>C	XP_024308239.1:p.Ala105=
NM_003611.3:c.1590T>C MANE Select	NP_003602.1:p.Ala530=
NM_001330209.2:c.1470T>C	NP_001317138.1:p.Ala490=
NM_001330210.2:c.1170T>C	NP_001317139.1:p.Ala390=