Canonical Allele Identifier: CA2416364088
Gene: OFD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.13736493C= , CM000685.2:g.13736493C= GRCh38
NC_000023.10:g.13754612C= , CM000685.1:g.13754612C= GRCh37
NC_000023.9:g.13664533C= NCBI36
NG_008872.1:g.6781C=
NG_011555.1:g.3131G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000380567.6:c.127C= ENSP00000369941.2:p.Gln43=
ENST00000398395.8:c.127C= ENSP00000381432.5:p.Gln43=
ENST00000464463.6:n.410C=
ENST00000485052.6:n.620C=
ENST00000490265.6:n.99C=
ENST00000682237.1:c.127C= ENSP00000507121.1:p.Gln43=
ENST00000682562.1:c.127C= ENSP00000507874.1:p.Gln43=
ENST00000682953.1:c.*190C= ENSP00000507878.1:n.*190C=
ENST00000683055.1:c.127C= ENSP00000508191.1:p.Gln43=
ENST00000683284.1:c.112-163C= ENSP00000507837.1:n.112-163C=
ENST00000683427.1:c.127C= ENSP00000507290.1:p.Gln43=
ENST00000683454.1:n.16C=
ENST00000683655.1:c.127C= ENSP00000506770.1:p.Gln43=
ENST00000683713.1:c.127C= ENSP00000507797.1:p.Gln43=
ENST00000684401.1:n.518C=
ENST00000684577.1:c.127C= ENSP00000507871.1:p.Gln43=
ENST00000340096.11:c.127C= MANE Select ENSP00000344314.6:p.Gln43=
ENST00000340096.10:c.127C= ENSP00000344314.6:p.Gln43=
ENST00000380550.6:c.127C= ENSP00000369923.3:p.Gln43=
ENST00000380567.5:c.-419C= ENSP00000369941.1:n.-419C=
ENST00000398395.7:c.-408C= ENSP00000381432.4:n.-408C=
ENST00000485052.5:n.631C=
ENST00000490265.5:n.438C=
NM_003611.2:c.127C= NP_003602.1:p.Gln43=
XM_005274599.2:c.148C= XP_005274656.1:p.Gln50=
XM_005274602.2:c.148C= XP_005274659.1:p.Gln50=
XM_005274603.2:c.148C= XP_005274660.1:p.Gln50=
XM_005274604.2:c.127C= XP_005274661.1:p.Gln43=
XM_005274606.2:c.-18C= XP_005274663.1:n.-18C=
XM_011545591.1:c.148C= XP_011543893.1:p.Gln50=
XM_011545592.1:c.98-163C= XP_011543894.1:n.98-163C=
XM_011545593.1:c.148C= XP_011543895.1:p.Gln50=
XM_011545594.1:c.-32-163C= XP_011543896.1:n.-32-163C=
XM_011545595.1:c.-32-163C= XP_011543897.1:n.-32-163C=
XM_011545596.1:c.148C= XP_011543898.1:p.Gln50=
XM_011545597.1:c.-419C= XP_011543899.1:n.-419C=
XR_247288.2:n.487C=
NM_001330209.1:c.127C= NP_001317138.1:p.Gln43=
NM_001330210.1:c.-419C= NP_001317139.1:n.-419C=
XM_005274606.4:c.-18C= XP_005274663.1:n.-18C=
XM_011545592.3:c.98-163C= XP_011543894.1:n.98-163C=
XM_011545594.3:c.-32-163C= XP_011543896.1:n.-32-163C=
XM_011545597.2:c.-419C= XP_011543899.1:n.-419C=
XM_017029909.1:c.-256-163C= XP_016885398.1:n.-256-163C=
XM_024452468.1:c.-1813C= XP_024308236.1:n.-1813C=
XM_024452469.1:c.-1813C= XP_024308237.1:n.-1813C=
XM_024452470.1:c.-1650-163C= XP_024308238.1:n.-1650-163C=
XM_024452471.1:c.-1813C= XP_024308239.1:n.-1813C=
NM_003611.3:c.127C= MANE Select NP_003602.1:p.Gln43=
NM_001330209.2:c.127C= NP_001317138.1:p.Gln43=
NM_001330210.2:c.-419C= NP_001317139.1:n.-419C=