Canonical Allele Identifier: CA10352062

Gene: OFD1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.13767199G>A , CM000685.2:g.13767199G>A	GRCh38
NC_000023.10:g.13785318G>A , CM000685.1:g.13785318G>A	GRCh37
NC_000023.9:g.13695239G>A	NCBI36
NG_008872.1:g.37487G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_003611.3:c.2672G>A MANE Select	NP_003602.1:p.Arg891Lys
ENST00000340096.11:c.2672G>A MANE Select	ENSP00000344314.6:p.Arg891Lys
NM_001330209.1:c.2552G>A	NP_001317138.1:p.Arg851Lys
NM_001330209.2:c.2552G>A	NP_001317138.1:p.Arg851Lys
NM_001330210.1:c.2252G>A	NP_001317139.1:p.Arg751Lys
NM_001330210.2:c.2252G>A	NP_001317139.1:p.Arg751Lys
NM_003611.2:c.2672G>A	NP_003602.1:p.Arg891Lys
ENST00000340096.10:c.2672G>A	ENSP00000344314.6:p.Arg891Lys
ENST00000380550.6:c.2552G>A	ENSP00000369923.3:p.Arg851Lys
ENST00000380567.5:c.2252G>A	ENSP00000369941.1:p.Arg751Lys
ENST00000380567.6:c.*2365G>A	ENSP00000369941.2:n.*2365G>A
ENST00000398395.7:c.*1012G>A	ENSP00000381432.4:n.*1012G>A
ENST00000398395.8:c.*2133G>A	ENSP00000381432.5:n.*2133G>A
ENST00000464463.5:n.382G>A
ENST00000464463.6:n.4501G>A
ENST00000490265.5:n.3647G>A
ENST00000490265.6:n.3201G>A
ENST00000682237.1:c.*2232G>A	ENSP00000507121.1:n.*2232G>A
ENST00000682562.1:c.*3963G>A	ENSP00000507874.1:n.*3963G>A
ENST00000682953.1:c.*3288G>A	ENSP00000507878.1:n.*3288G>A
ENST00000683055.1:c.*3542G>A	ENSP00000508191.1:n.*3542G>A
ENST00000683284.1:c.*2903G>A	ENSP00000507837.1:n.*2903G>A
ENST00000683427.1:c.*1329G>A	ENSP00000507290.1:n.*1329G>A
ENST00000683454.1:n.2686G>A
ENST00000683637.1:n.3781G>A
ENST00000683655.1:c.*2886G>A	ENSP00000506770.1:n.*2886G>A
ENST00000683713.1:c.*2903G>A	ENSP00000507797.1:n.*2903G>A
ENST00000684577.1:c.*2258G>A	ENSP00000507871.1:n.*2258G>A
XM_005274599.2:c.2693G>A	XP_005274656.1:p.Arg898Lys
XM_005274602.2:c.2582G>A	XP_005274659.1:p.Arg861Lys
XM_005274603.2:c.2573G>A	XP_005274660.1:p.Arg858Lys
XM_005274604.2:c.2552G>A	XP_005274661.1:p.Arg851Lys
XM_005274606.2:c.2528G>A	XP_005274663.1:p.Arg843Lys
XM_005274606.4:c.2528G>A	XP_005274663.1:p.Arg843Lys
XM_005274607.3:c.2252G>A	XP_005274664.1:p.Arg751Lys
XM_011545591.1:c.2693G>A	XP_011543893.1:p.Arg898Lys
XM_011545592.1:c.2480G>A	XP_011543894.1:p.Arg827Lys
XM_011545592.3:c.2480G>A	XP_011543894.1:p.Arg827Lys
XM_011545593.1:c.2693G>A	XP_011543895.1:p.Arg898Lys
XM_011545594.1:c.2351G>A	XP_011543896.1:p.Arg784Lys
XM_011545594.3:c.2351G>A	XP_011543896.1:p.Arg784Lys
XM_011545595.1:c.2351G>A	XP_011543897.1:p.Arg784Lys
XM_011545596.1:c.2510-855G>A	XP_011543898.1:n.2510-855G>A
XM_011545597.1:c.2141G>A	XP_011543899.1:p.Arg714Lys
XM_011545597.2:c.2141G>A	XP_011543899.1:p.Arg714Lys
XM_011545598.1:c.1397G>A	XP_011543900.1:p.Arg466Lys
XM_017029909.1:c.2252G>A	XP_016885398.1:p.Arg751Lys
XM_017029911.1:c.1730G>A	XP_016885400.1:p.Arg577Lys
XM_024452468.1:c.1397G>A	XP_024308236.1:p.Arg466Lys
XM_024452469.1:c.1397G>A	XP_024308237.1:p.Arg466Lys
XM_024452470.1:c.1397G>A	XP_024308238.1:p.Arg466Lys
XM_024452471.1:c.1286G>A	XP_024308239.1:p.Arg429Lys
XR_247288.2:n.2960-855G>A