Canonical Allele Identifier: CA412343436

Gene: OFD1

Linked Data

• MyVariant Identifiers: chrX:g.13776531G>T (hg19) ; chrX:g.13758412G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.13758412G>T , CM000685.2:g.13758412G>T	GRCh38
NC_000023.10:g.13776531G>T , CM000685.1:g.13776531G>T	GRCh37
NC_000023.9:g.13686452G>T	NCBI36
NG_008872.1:g.28700G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380567.6:c.*1311G>T	ENSP00000369941.2:n.*1311G>T
ENST00000398395.8:c.*1115+622G>T	ENSP00000381432.5:n.*1115+622G>T
ENST00000464463.6:n.1781G>T
ENST00000490265.6:n.2147G>T
ENST00000682237.1:c.*1178G>T	ENSP00000507121.1:n.*1178G>T
ENST00000682562.1:c.*3020G>T	ENSP00000507874.1:n.*3020G>T
ENST00000682953.1:c.*2345G>T	ENSP00000507878.1:n.*2345G>T
ENST00000683055.1:c.*933G>T	ENSP00000508191.1:n.*933G>T
ENST00000683284.1:c.*1849G>T	ENSP00000507837.1:n.*1849G>T
ENST00000683427.1:c.*311+622G>T	ENSP00000507290.1:n.*311+622G>T
ENST00000683454.1:n.1632G>T
ENST00000683637.1:n.2727G>T
ENST00000683655.1:c.*1832G>T	ENSP00000506770.1:n.*1832G>T
ENST00000683713.1:c.*1849G>T	ENSP00000507797.1:n.*1849G>T
ENST00000684577.1:c.*1315G>T	ENSP00000507871.1:n.*1315G>T
ENST00000340096.11:c.1618G>T MANE Select	ENSP00000344314.6:p.Ala540Ser
ENST00000340096.10:c.1618G>T	ENSP00000344314.6:p.Ala540Ser
ENST00000380550.6:c.1498G>T	ENSP00000369923.3:p.Ala500Ser
ENST00000380567.5:c.1198G>T	ENSP00000369941.1:p.Ala400Ser
ENST00000398395.7:c.1011+622G>T	ENSP00000381432.4:n.1011+622G>T
ENST00000490265.5:n.2593G>T
NM_003611.2:c.1618G>T	NP_003602.1:p.Ala540Ser
XM_005274599.2:c.1639G>T	XP_005274656.1:p.Ala547Ser
XM_005274602.2:c.1639G>T	XP_005274659.1:p.Ala547Ser
XM_005274603.2:c.1519G>T	XP_005274660.1:p.Ala507Ser
XM_005274604.2:c.1498G>T	XP_005274661.1:p.Ala500Ser
XM_005274606.2:c.1474G>T	XP_005274663.1:p.Ala492Ser
XM_005274607.3:c.1198G>T	XP_005274664.1:p.Ala400Ser
XM_011545591.1:c.1639G>T	XP_011543893.1:p.Ala547Ser
XM_011545592.1:c.1426G>T	XP_011543894.1:p.Ala476Ser
XM_011545593.1:c.1639G>T	XP_011543895.1:p.Ala547Ser
XM_011545594.1:c.1297G>T	XP_011543896.1:p.Ala433Ser
XM_011545595.1:c.1297G>T	XP_011543897.1:p.Ala433Ser
XM_011545596.1:c.1639G>T	XP_011543898.1:p.Ala547Ser
XM_011545597.1:c.1198G>T	XP_011543899.1:p.Ala400Ser
XM_011545598.1:c.343G>T	XP_011543900.1:p.Ala115Ser
XR_247288.2:n.1978G>T
NM_001330209.1:c.1498G>T	NP_001317138.1:p.Ala500Ser
NM_001330210.1:c.1198G>T	NP_001317139.1:p.Ala400Ser
XM_005274606.4:c.1474G>T	XP_005274663.1:p.Ala492Ser
XM_011545592.3:c.1426G>T	XP_011543894.1:p.Ala476Ser
XM_011545594.3:c.1297G>T	XP_011543896.1:p.Ala433Ser
XM_011545597.2:c.1198G>T	XP_011543899.1:p.Ala400Ser
XM_017029909.1:c.1198G>T	XP_016885398.1:p.Ala400Ser
XM_017029911.1:c.676G>T	XP_016885400.1:p.Ala226Ser
XM_024452468.1:c.343G>T	XP_024308236.1:p.Ala115Ser
XM_024452469.1:c.343G>T	XP_024308237.1:p.Ala115Ser
XM_024452470.1:c.343G>T	XP_024308238.1:p.Ala115Ser
XM_024452471.1:c.343G>T	XP_024308239.1:p.Ala115Ser
NM_003611.3:c.1618G>T MANE Select	NP_003602.1:p.Ala540Ser
NM_001330209.2:c.1498G>T	NP_001317138.1:p.Ala500Ser
NM_001330210.2:c.1198G>T	NP_001317139.1:p.Ala400Ser