Canonical Allele Identifier: CA344013
Gene: OFD1 HGNC NCBI

Linked Data

dbSNP Id: rs312262831

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.13739031del , CM000685.2:g.13739031del GRCh38
NC_000023.10:g.13757150del , CM000685.1:g.13757150del GRCh37
NC_000023.9:g.13667071del NCBI36
NG_008872.1:g.9319del
NG_011555.1:g.597del

Transcript Alleles

HGVS Amino-acid change
ENST00000380567.6:c.411del ENSP00000369941.2:p.Ala138ProfsTer5
ENST00000398395.8:c.411del ENSP00000381432.5:p.Ala138ProfsTer5
ENST00000464463.6:n.694del
ENST00000490265.6:n.273del
ENST00000682237.1:c.411del ENSP00000507121.1:p.Gly138ValfsTer7
ENST00000682562.1:c.411del ENSP00000507874.1:p.Ala138ProfsTer5
ENST00000682953.1:c.*474del ENSP00000507878.1:n.*474del
ENST00000683055.1:c.411del ENSP00000508191.1:p.Ala138LeufsTer24
ENST00000683284.1:c.233del ENSP00000507837.1:p.Lys78ArgfsTer17
ENST00000683427.1:c.411del ENSP00000507290.1:p.Gly138ValfsTer7
ENST00000683454.1:n.300del
ENST00000683655.1:c.411del ENSP00000506770.1:p.Gly138ValfsTer7
ENST00000683713.1:c.312+2353del ENSP00000507797.1:n.312+2353del
ENST00000684401.1:n.802del
ENST00000684577.1:c.411del ENSP00000507871.1:p.Ala138ProfsTer5
ENST00000340096.11:c.411del MANE Select ENSP00000344314.6:p.Gly138ValfsTer7
ENST00000340096.10:c.411del ENSP00000344314.6:p.Gly138ValfsTer7
ENST00000380550.6:c.411del ENSP00000369923.3:p.Gly138ValfsTer7
ENST00000380567.5:c.-135del ENSP00000369941.1:n.-135del
ENST00000398395.7:c.-124del ENSP00000381432.4:n.-124del
ENST00000466534.1:n.251del
ENST00000490265.5:n.722del
NM_003611.2:c.411del NP_003602.1:p.Gly138ValfsTer7
XM_005274599.2:c.432del XP_005274656.1:p.Gly145ValfsTer7
XM_005274602.2:c.432del XP_005274659.1:p.Gly145ValfsTer7
XM_005274603.2:c.432del XP_005274660.1:p.Gly145ValfsTer7
XM_005274604.2:c.411del XP_005274661.1:p.Gly138ValfsTer7
XM_005274606.2:c.267del XP_005274663.1:p.Gly90ValfsTer7
XM_011545591.1:c.432del XP_011543893.1:p.Gly145ValfsTer7
XM_011545592.1:c.219del XP_011543894.1:p.Gly74ValfsTer7
XM_011545593.1:c.432del XP_011543895.1:p.Gly145ValfsTer7
XM_011545594.1:c.90del XP_011543896.1:p.Gly31ValfsTer7
XM_011545595.1:c.90del XP_011543897.1:p.Gly31ValfsTer7
XM_011545596.1:c.432del XP_011543898.1:p.Gly145ValfsTer7
XM_011545597.1:c.-135del XP_011543899.1:n.-135del
XR_247288.2:n.771del
NM_001330209.1:c.411del NP_001317138.1:p.Gly138ValfsTer7
NM_001330210.1:c.-135del NP_001317139.1:n.-135del
XM_005274606.4:c.267del XP_005274663.1:p.Gly90ValfsTer7
XM_011545592.3:c.219del XP_011543894.1:p.Gly74ValfsTer7
XM_011545594.3:c.90del XP_011543896.1:p.Gly31ValfsTer7
XM_011545597.2:c.-135del XP_011543899.1:n.-135del
XM_017029909.1:c.-135del XP_016885398.1:n.-135del
XM_024452468.1:c.-1529del XP_024308236.1:n.-1529del
XM_024452469.1:c.-1529del XP_024308237.1:n.-1529del
XM_024452470.1:c.-1529del XP_024308238.1:n.-1529del
XM_024452471.1:c.-1529del XP_024308239.1:n.-1529del
NM_003611.3:c.411del MANE Select NP_003602.1:p.Gly138ValfsTer7
NM_001330209.2:c.411del NP_001317138.1:p.Gly138ValfsTer7
NM_001330210.2:c.-135del NP_001317139.1:n.-135del