Canonical Allele Identifier: CA344012
Gene: OFD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 41117
dbSNP Id: rs312262830

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.13739020_13739023del , CM000685.2:g.13739020_13739023del GRCh38
NC_000023.10:g.13757139_13757142del , CM000685.1:g.13757139_13757142del GRCh37
NC_000023.9:g.13667060_13667063del NCBI36
NG_008872.1:g.9308_9311del
NG_011555.1:g.604_607del

Transcript Alleles

HGVS Amino-acid change
ENST00000380567.6:c.400_403del ENSP00000369941.2:p.Glu134IlefsTer8
ENST00000398395.8:c.400_403del ENSP00000381432.5:p.Glu134IlefsTer8
ENST00000464463.6:n.683_686del
ENST00000490265.6:n.262_265del
ENST00000682237.1:c.400_403del ENSP00000507121.1:p.Glu134IlefsTer10
ENST00000682562.1:c.400_403del ENSP00000507874.1:p.Glu134IlefsTer8
ENST00000682953.1:c.*463_*466del ENSP00000507878.1:n.*463_*466del
ENST00000683055.1:c.400_403del ENSP00000508191.1:p.Glu134IlefsTer27
ENST00000683284.1:c.222_225del ENSP00000507837.1:p.Lys75SerfsTer19
ENST00000683427.1:c.400_403del ENSP00000507290.1:p.Glu134IlefsTer10
ENST00000683454.1:n.289_292del
ENST00000683655.1:c.400_403del ENSP00000506770.1:p.Glu134IlefsTer10
ENST00000683713.1:c.312+2342_312+2345del ENSP00000507797.1:n.312+2342_312+2345del
ENST00000684401.1:n.791_794del
ENST00000684577.1:c.400_403del ENSP00000507871.1:p.Glu134IlefsTer8
ENST00000340096.11:c.400_403del MANE Select ENSP00000344314.6:p.Glu134IlefsTer10
ENST00000340096.10:c.400_403del ENSP00000344314.6:p.Glu134IlefsTer10
ENST00000380550.6:c.400_403del ENSP00000369923.3:p.Glu134IlefsTer10
ENST00000380567.5:c.-146_-143del ENSP00000369941.1:n.-146_-143del
ENST00000398395.7:c.-135_-132del ENSP00000381432.4:n.-135_-132del
ENST00000466534.1:n.240_243del
ENST00000490265.5:n.711_714del
NM_003611.2:c.400_403del NP_003602.1:p.Glu134IlefsTer10
XM_005274599.2:c.421_424del XP_005274656.1:p.Glu141IlefsTer10
XM_005274602.2:c.421_424del XP_005274659.1:p.Glu141IlefsTer10
XM_005274603.2:c.421_424del XP_005274660.1:p.Glu141IlefsTer10
XM_005274604.2:c.400_403del XP_005274661.1:p.Glu134IlefsTer10
XM_005274606.2:c.256_259del XP_005274663.1:p.Glu86IlefsTer10
XM_011545591.1:c.421_424del XP_011543893.1:p.Glu141IlefsTer10
XM_011545592.1:c.208_211del XP_011543894.1:p.Glu70IlefsTer10
XM_011545593.1:c.421_424del XP_011543895.1:p.Glu141IlefsTer10
XM_011545594.1:c.79_82del XP_011543896.1:p.Glu27IlefsTer10
XM_011545595.1:c.79_82del XP_011543897.1:p.Glu27IlefsTer10
XM_011545596.1:c.421_424del XP_011543898.1:p.Glu141IlefsTer10
XM_011545597.1:c.-146_-143del XP_011543899.1:n.-146_-143del
XR_247288.2:n.760_763del
NM_001330209.1:c.400_403del NP_001317138.1:p.Glu134IlefsTer10
NM_001330210.1:c.-146_-143del NP_001317139.1:n.-146_-143del
XM_005274606.4:c.256_259del XP_005274663.1:p.Glu86IlefsTer10
XM_011545592.3:c.208_211del XP_011543894.1:p.Glu70IlefsTer10
XM_011545594.3:c.79_82del XP_011543896.1:p.Glu27IlefsTer10
XM_011545597.2:c.-146_-143del XP_011543899.1:n.-146_-143del
XM_017029909.1:c.-146_-143del XP_016885398.1:n.-146_-143del
XM_024452468.1:c.-1540_-1537del XP_024308236.1:n.-1540_-1537del
XM_024452469.1:c.-1540_-1537del XP_024308237.1:n.-1540_-1537del
XM_024452470.1:c.-1540_-1537del XP_024308238.1:n.-1540_-1537del
XM_024452471.1:c.-1540_-1537del XP_024308239.1:n.-1540_-1537del
NM_003611.3:c.400_403del MANE Select NP_003602.1:p.Glu134IlefsTer10
NM_001330209.2:c.400_403del NP_001317138.1:p.Glu134IlefsTer10
NM_001330210.2:c.-146_-143del NP_001317139.1:n.-146_-143del