Canonical Allele Identifier: CA10351673

Gene: OFD1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.13746804A>G , CM000685.2:g.13746804A>G	GRCh38
NC_000023.10:g.13764923A>G , CM000685.1:g.13764923A>G	GRCh37
NC_000023.9:g.13674844A>G	NCBI36
NG_008872.1:g.17092A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380567.6:c.*372A>G	ENSP00000369941.2:n.*372A>G
ENST00000398395.8:c.*372A>G	ENSP00000381432.5:n.*372A>G
ENST00000464463.6:n.962A>G
ENST00000490265.6:n.541A>G
ENST00000682237.1:c.679A>G	ENSP00000507121.1:p.Ile227Val
ENST00000682562.1:c.*372A>G	ENSP00000507874.1:n.*372A>G
ENST00000682953.1:c.*742A>G	ENSP00000507878.1:n.*742A>G
ENST00000683055.1:c.574A>G	ENSP00000508191.1:p.Ile192Val
ENST00000683065.1:n.88A>G
ENST00000683284.1:c.*246A>G	ENSP00000507837.1:n.*246A>G
ENST00000683427.1:c.679A>G	ENSP00000507290.1:p.Ile227Val
ENST00000683454.1:n.693A>G
ENST00000683637.1:n.1124A>G
ENST00000683655.1:c.*229A>G	ENSP00000506770.1:n.*229A>G
ENST00000683713.1:c.*246A>G	ENSP00000507797.1:n.*246A>G
ENST00000684577.1:c.*372A>G	ENSP00000507871.1:n.*372A>G
ENST00000340096.11:c.679A>G MANE Select	ENSP00000344314.6:p.Ile227Val
ENST00000340096.10:c.679A>G	ENSP00000344314.6:p.Ile227Val
ENST00000380550.6:c.679A>G	ENSP00000369923.3:p.Ile227Val
ENST00000380567.5:c.259A>G	ENSP00000369941.1:p.Ile87Val
ENST00000398395.7:c.268A>G	ENSP00000381432.4:p.Ile90Val
ENST00000490265.5:n.990A>G
NM_003611.2:c.679A>G	NP_003602.1:p.Ile227Val
XM_005274599.2:c.700A>G	XP_005274656.1:p.Ile234Val
XM_005274602.2:c.700A>G	XP_005274659.1:p.Ile234Val
XM_005274603.2:c.700A>G	XP_005274660.1:p.Ile234Val
XM_005274604.2:c.679A>G	XP_005274661.1:p.Ile227Val
XM_005274606.2:c.535A>G	XP_005274663.1:p.Ile179Val
XM_005274607.3:c.259A>G	XP_005274664.1:p.Ile87Val
XM_011545591.1:c.700A>G	XP_011543893.1:p.Ile234Val
XM_011545592.1:c.487A>G	XP_011543894.1:p.Ile163Val
XM_011545593.1:c.700A>G	XP_011543895.1:p.Ile234Val
XM_011545594.1:c.358A>G	XP_011543896.1:p.Ile120Val
XM_011545595.1:c.358A>G	XP_011543897.1:p.Ile120Val
XM_011545596.1:c.700A>G	XP_011543898.1:p.Ile234Val
XM_011545597.1:c.259A>G	XP_011543899.1:p.Ile87Val
XR_247288.2:n.1039A>G
NM_001330209.1:c.679A>G	NP_001317138.1:p.Ile227Val
NM_001330210.1:c.259A>G	NP_001317139.1:p.Ile87Val
XM_005274606.4:c.535A>G	XP_005274663.1:p.Ile179Val
XM_011545592.3:c.487A>G	XP_011543894.1:p.Ile163Val
XM_011545594.3:c.358A>G	XP_011543896.1:p.Ile120Val
XM_011545597.2:c.259A>G	XP_011543899.1:p.Ile87Val
XM_017029909.1:c.259A>G	XP_016885398.1:p.Ile87Val
XM_024452468.1:c.-1261A>G	XP_024308236.1:n.-1261A>G
XM_024452469.1:c.-1261A>G	XP_024308237.1:n.-1261A>G
XM_024452470.1:c.-1261A>G	XP_024308238.1:n.-1261A>G
XM_024452471.1:c.-1261A>G	XP_024308239.1:n.-1261A>G
NM_003611.3:c.679A>G MANE Select	NP_003602.1:p.Ile227Val
NM_001330209.2:c.679A>G	NP_001317138.1:p.Ile227Val
NM_001330210.2:c.259A>G	NP_001317139.1:p.Ile87Val