Canonical Allele Identifier: CA412343466

Gene: OFD1

Linked Data

• MyVariant Identifiers: chrX:g.13776545G>T (hg19) ; chrX:g.13758426G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.13758426G>T , CM000685.2:g.13758426G>T	GRCh38
NC_000023.10:g.13776545G>T , CM000685.1:g.13776545G>T	GRCh37
NC_000023.9:g.13686466G>T	NCBI36
NG_008872.1:g.28714G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380567.6:c.*1325G>T	ENSP00000369941.2:n.*1325G>T
ENST00000398395.8:c.*1115+636G>T	ENSP00000381432.5:n.*1115+636G>T
ENST00000464463.6:n.1795G>T
ENST00000490265.6:n.2161G>T
ENST00000682237.1:c.*1192G>T	ENSP00000507121.1:n.*1192G>T
ENST00000682562.1:c.*3034G>T	ENSP00000507874.1:n.*3034G>T
ENST00000682953.1:c.*2359G>T	ENSP00000507878.1:n.*2359G>T
ENST00000683055.1:c.*947G>T	ENSP00000508191.1:n.*947G>T
ENST00000683284.1:c.*1863G>T	ENSP00000507837.1:n.*1863G>T
ENST00000683427.1:c.*311+636G>T	ENSP00000507290.1:n.*311+636G>T
ENST00000683454.1:n.1646G>T
ENST00000683637.1:n.2741G>T
ENST00000683655.1:c.*1846G>T	ENSP00000506770.1:n.*1846G>T
ENST00000683713.1:c.*1863G>T	ENSP00000507797.1:n.*1863G>T
ENST00000684577.1:c.*1329G>T	ENSP00000507871.1:n.*1329G>T
ENST00000340096.11:c.1632G>T MANE Select	ENSP00000344314.6:p.Leu544Phe
ENST00000340096.10:c.1632G>T	ENSP00000344314.6:p.Leu544Phe
ENST00000380550.6:c.1512G>T	ENSP00000369923.3:p.Leu504Phe
ENST00000380567.5:c.1212G>T	ENSP00000369941.1:p.Leu404Phe
ENST00000398395.7:c.1011+636G>T	ENSP00000381432.4:n.1011+636G>T
ENST00000490265.5:n.2607G>T
NM_003611.2:c.1632G>T	NP_003602.1:p.Leu544Phe
XM_005274599.2:c.1653G>T	XP_005274656.1:p.Leu551Phe
XM_005274602.2:c.1653G>T	XP_005274659.1:p.Leu551Phe
XM_005274603.2:c.1533G>T	XP_005274660.1:p.Leu511Phe
XM_005274604.2:c.1512G>T	XP_005274661.1:p.Leu504Phe
XM_005274606.2:c.1488G>T	XP_005274663.1:p.Leu496Phe
XM_005274607.3:c.1212G>T	XP_005274664.1:p.Leu404Phe
XM_011545591.1:c.1653G>T	XP_011543893.1:p.Leu551Phe
XM_011545592.1:c.1440G>T	XP_011543894.1:p.Leu480Phe
XM_011545593.1:c.1653G>T	XP_011543895.1:p.Leu551Phe
XM_011545594.1:c.1311G>T	XP_011543896.1:p.Leu437Phe
XM_011545595.1:c.1311G>T	XP_011543897.1:p.Leu437Phe
XM_011545596.1:c.1653G>T	XP_011543898.1:p.Leu551Phe
XM_011545597.1:c.1212G>T	XP_011543899.1:p.Leu404Phe
XM_011545598.1:c.357G>T	XP_011543900.1:p.Leu119Phe
XR_247288.2:n.1992G>T
NM_001330209.1:c.1512G>T	NP_001317138.1:p.Leu504Phe
NM_001330210.1:c.1212G>T	NP_001317139.1:p.Leu404Phe
XM_005274606.4:c.1488G>T	XP_005274663.1:p.Leu496Phe
XM_011545592.3:c.1440G>T	XP_011543894.1:p.Leu480Phe
XM_011545594.3:c.1311G>T	XP_011543896.1:p.Leu437Phe
XM_011545597.2:c.1212G>T	XP_011543899.1:p.Leu404Phe
XM_017029909.1:c.1212G>T	XP_016885398.1:p.Leu404Phe
XM_017029911.1:c.690G>T	XP_016885400.1:p.Leu230Phe
XM_024452468.1:c.357G>T	XP_024308236.1:p.Leu119Phe
XM_024452469.1:c.357G>T	XP_024308237.1:p.Leu119Phe
XM_024452470.1:c.357G>T	XP_024308238.1:p.Leu119Phe
XM_024452471.1:c.357G>T	XP_024308239.1:p.Leu119Phe
NM_003611.3:c.1632G>T MANE Select	NP_003602.1:p.Leu544Phe
NM_001330209.2:c.1512G>T	NP_001317138.1:p.Leu504Phe
NM_001330210.2:c.1212G>T	NP_001317139.1:p.Leu404Phe