Canonical Allele Identifier: CA412343473

Gene: OFD1

Linked Data

• gnomAD v4: X-13758430-C-A
• MyVariant Identifiers: chrX:g.13776549C>A (hg19) ; chrX:g.13758430C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.13758430C>A , CM000685.2:g.13758430C>A	GRCh38
NC_000023.10:g.13776549C>A , CM000685.1:g.13776549C>A	GRCh37
NC_000023.9:g.13686470C>A	NCBI36
NG_008872.1:g.28718C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380567.6:c.*1329C>A	ENSP00000369941.2:n.*1329C>A
ENST00000398395.8:c.*1115+640C>A	ENSP00000381432.5:n.*1115+640C>A
ENST00000464463.6:n.1799C>A
ENST00000490265.6:n.2165C>A
ENST00000682237.1:c.*1196C>A	ENSP00000507121.1:n.*1196C>A
ENST00000682562.1:c.*3038C>A	ENSP00000507874.1:n.*3038C>A
ENST00000682953.1:c.*2363C>A	ENSP00000507878.1:n.*2363C>A
ENST00000683055.1:c.*951C>A	ENSP00000508191.1:n.*951C>A
ENST00000683284.1:c.*1867C>A	ENSP00000507837.1:n.*1867C>A
ENST00000683427.1:c.*311+640C>A	ENSP00000507290.1:n.*311+640C>A
ENST00000683454.1:n.1650C>A
ENST00000683637.1:n.2745C>A
ENST00000683655.1:c.*1850C>A	ENSP00000506770.1:n.*1850C>A
ENST00000683713.1:c.*1867C>A	ENSP00000507797.1:n.*1867C>A
ENST00000684577.1:c.*1333C>A	ENSP00000507871.1:n.*1333C>A
ENST00000340096.11:c.1636C>A MANE Select	ENSP00000344314.6:p.Leu546Met
ENST00000340096.10:c.1636C>A	ENSP00000344314.6:p.Leu546Met
ENST00000380550.6:c.1516C>A	ENSP00000369923.3:p.Leu506Met
ENST00000380567.5:c.1216C>A	ENSP00000369941.1:p.Leu406Met
ENST00000398395.7:c.1011+640C>A	ENSP00000381432.4:n.1011+640C>A
ENST00000490265.5:n.2611C>A
NM_003611.2:c.1636C>A	NP_003602.1:p.Leu546Met
XM_005274599.2:c.1657C>A	XP_005274656.1:p.Leu553Met
XM_005274602.2:c.1657C>A	XP_005274659.1:p.Leu553Met
XM_005274603.2:c.1537C>A	XP_005274660.1:p.Leu513Met
XM_005274604.2:c.1516C>A	XP_005274661.1:p.Leu506Met
XM_005274606.2:c.1492C>A	XP_005274663.1:p.Leu498Met
XM_005274607.3:c.1216C>A	XP_005274664.1:p.Leu406Met
XM_011545591.1:c.1657C>A	XP_011543893.1:p.Leu553Met
XM_011545592.1:c.1444C>A	XP_011543894.1:p.Leu482Met
XM_011545593.1:c.1657C>A	XP_011543895.1:p.Leu553Met
XM_011545594.1:c.1315C>A	XP_011543896.1:p.Leu439Met
XM_011545595.1:c.1315C>A	XP_011543897.1:p.Leu439Met
XM_011545596.1:c.1657C>A	XP_011543898.1:p.Leu553Met
XM_011545597.1:c.1216C>A	XP_011543899.1:p.Leu406Met
XM_011545598.1:c.361C>A	XP_011543900.1:p.Leu121Met
XR_247288.2:n.1996C>A
NM_001330209.1:c.1516C>A	NP_001317138.1:p.Leu506Met
NM_001330210.1:c.1216C>A	NP_001317139.1:p.Leu406Met
XM_005274606.4:c.1492C>A	XP_005274663.1:p.Leu498Met
XM_011545592.3:c.1444C>A	XP_011543894.1:p.Leu482Met
XM_011545594.3:c.1315C>A	XP_011543896.1:p.Leu439Met
XM_011545597.2:c.1216C>A	XP_011543899.1:p.Leu406Met
XM_017029909.1:c.1216C>A	XP_016885398.1:p.Leu406Met
XM_017029911.1:c.694C>A	XP_016885400.1:p.Leu232Met
XM_024452468.1:c.361C>A	XP_024308236.1:p.Leu121Met
XM_024452469.1:c.361C>A	XP_024308237.1:p.Leu121Met
XM_024452470.1:c.361C>A	XP_024308238.1:p.Leu121Met
XM_024452471.1:c.361C>A	XP_024308239.1:p.Leu121Met
NM_003611.3:c.1636C>A MANE Select	NP_003602.1:p.Leu546Met
NM_001330209.2:c.1516C>A	NP_001317138.1:p.Leu506Met
NM_001330210.2:c.1216C>A	NP_001317139.1:p.Leu406Met