Canonical Allele Identifier: CA343976
Gene: OFD1 HGNC NCBI

Linked Data

dbSNP Id: rs312262883

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.13758381del , CM000685.2:g.13758381del GRCh38
NC_000023.10:g.13776500del , CM000685.1:g.13776500del GRCh37
NC_000023.9:g.13686421del NCBI36
NG_008872.1:g.28669del

Transcript Alleles

HGVS Amino-acid change
ENST00000380567.6:c.*1280del ENSP00000369941.2:n.*1280del
ENST00000398395.8:c.*1115+591del ENSP00000381432.5:n.*1115+591del
ENST00000464463.6:n.1750del
ENST00000490265.6:n.2116del
ENST00000682237.1:c.*1147del ENSP00000507121.1:n.*1147del
ENST00000682562.1:c.*2989del ENSP00000507874.1:n.*2989del
ENST00000682953.1:c.*2314del ENSP00000507878.1:n.*2314del
ENST00000683055.1:c.*902del ENSP00000508191.1:n.*902del
ENST00000683284.1:c.*1818del ENSP00000507837.1:n.*1818del
ENST00000683427.1:c.*311+591del ENSP00000507290.1:n.*311+591del
ENST00000683454.1:n.1601del
ENST00000683637.1:n.2696del
ENST00000683655.1:c.*1801del ENSP00000506770.1:n.*1801del
ENST00000683713.1:c.*1818del ENSP00000507797.1:n.*1818del
ENST00000684577.1:c.*1284del ENSP00000507871.1:n.*1284del
ENST00000340096.11:c.1587del MANE Select ENSP00000344314.6:p.Ala530LeufsTer3
ENST00000340096.10:c.1587del ENSP00000344314.6:p.Ala530LeufsTer3
ENST00000380550.6:c.1467del ENSP00000369923.3:p.Ala490LeufsTer3
ENST00000380567.5:c.1167del ENSP00000369941.1:p.Ala390LeufsTer3
ENST00000398395.7:c.1011+591del ENSP00000381432.4:n.1011+591del
ENST00000490265.5:n.2562del
NM_003611.2:c.1587del NP_003602.1:p.Ala530LeufsTer3
XM_005274599.2:c.1608del XP_005274656.1:p.Ala537LeufsTer3
XM_005274602.2:c.1608del XP_005274659.1:p.Ala537LeufsTer3
XM_005274603.2:c.1488del XP_005274660.1:p.Ala497LeufsTer3
XM_005274604.2:c.1467del XP_005274661.1:p.Ala490LeufsTer3
XM_005274606.2:c.1443del XP_005274663.1:p.Ala482LeufsTer3
XM_005274607.3:c.1167del XP_005274664.1:p.Ala390LeufsTer3
XM_011545591.1:c.1608del XP_011543893.1:p.Ala537LeufsTer3
XM_011545592.1:c.1395del XP_011543894.1:p.Ala466LeufsTer3
XM_011545593.1:c.1608del XP_011543895.1:p.Ala537LeufsTer3
XM_011545594.1:c.1266del XP_011543896.1:p.Ala423LeufsTer3
XM_011545595.1:c.1266del XP_011543897.1:p.Ala423LeufsTer3
XM_011545596.1:c.1608del XP_011543898.1:p.Ala537LeufsTer3
XM_011545597.1:c.1167del XP_011543899.1:p.Ala390LeufsTer3
XM_011545598.1:c.312del XP_011543900.1:p.Ala105LeufsTer3
XR_247288.2:n.1947del
NM_001330209.1:c.1467del NP_001317138.1:p.Ala490LeufsTer3
NM_001330210.1:c.1167del NP_001317139.1:p.Ala390LeufsTer3
XM_005274606.4:c.1443del XP_005274663.1:p.Ala482LeufsTer3
XM_011545592.3:c.1395del XP_011543894.1:p.Ala466LeufsTer3
XM_011545594.3:c.1266del XP_011543896.1:p.Ala423LeufsTer3
XM_011545597.2:c.1167del XP_011543899.1:p.Ala390LeufsTer3
XM_017029909.1:c.1167del XP_016885398.1:p.Ala390LeufsTer3
XM_017029911.1:c.645del XP_016885400.1:p.Ala216LeufsTer3
XM_024452468.1:c.312del XP_024308236.1:p.Ala105LeufsTer3
XM_024452469.1:c.312del XP_024308237.1:p.Ala105LeufsTer3
XM_024452470.1:c.312del XP_024308238.1:p.Ala105LeufsTer3
XM_024452471.1:c.312del XP_024308239.1:p.Ala105LeufsTer3
NM_003611.3:c.1587del MANE Select NP_003602.1:p.Ala530LeufsTer3
NM_001330209.2:c.1467del NP_001317138.1:p.Ala490LeufsTer3
NM_001330210.2:c.1167del NP_001317139.1:p.Ala390LeufsTer3