Canonical Allele Identifier: CA412343498

Gene: OFD1

Linked Data

• gnomAD v4: X-13758440-C-A
• MyVariant Identifiers: chrX:g.13776559C>A (hg19) ; chrX:g.13758440C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.13758440C>A , CM000685.2:g.13758440C>A	GRCh38
NC_000023.10:g.13776559C>A , CM000685.1:g.13776559C>A	GRCh37
NC_000023.9:g.13686480C>A	NCBI36
NG_008872.1:g.28728C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380567.6:c.*1339C>A	ENSP00000369941.2:n.*1339C>A
ENST00000398395.8:c.*1115+650C>A	ENSP00000381432.5:n.*1115+650C>A
ENST00000464463.6:n.1809C>A
ENST00000490265.6:n.2175C>A
ENST00000682237.1:c.*1206C>A	ENSP00000507121.1:n.*1206C>A
ENST00000682562.1:c.*3048C>A	ENSP00000507874.1:n.*3048C>A
ENST00000682953.1:c.*2373C>A	ENSP00000507878.1:n.*2373C>A
ENST00000683055.1:c.*961C>A	ENSP00000508191.1:n.*961C>A
ENST00000683284.1:c.*1877C>A	ENSP00000507837.1:n.*1877C>A
ENST00000683427.1:c.*311+650C>A	ENSP00000507290.1:n.*311+650C>A
ENST00000683454.1:n.1660C>A
ENST00000683637.1:n.2755C>A
ENST00000683655.1:c.*1860C>A	ENSP00000506770.1:n.*1860C>A
ENST00000683713.1:c.*1877C>A	ENSP00000507797.1:n.*1877C>A
ENST00000684577.1:c.*1343C>A	ENSP00000507871.1:n.*1343C>A
ENST00000340096.11:c.1646C>A MANE Select	ENSP00000344314.6:p.Thr549Asn
ENST00000340096.10:c.1646C>A	ENSP00000344314.6:p.Thr549Asn
ENST00000380550.6:c.1526C>A	ENSP00000369923.3:p.Thr509Asn
ENST00000380567.5:c.1226C>A	ENSP00000369941.1:p.Thr409Asn
ENST00000398395.7:c.1011+650C>A	ENSP00000381432.4:n.1011+650C>A
ENST00000490265.5:n.2621C>A
NM_003611.2:c.1646C>A	NP_003602.1:p.Thr549Asn
XM_005274599.2:c.1667C>A	XP_005274656.1:p.Thr556Asn
XM_005274602.2:c.1667C>A	XP_005274659.1:p.Thr556Asn
XM_005274603.2:c.1547C>A	XP_005274660.1:p.Thr516Asn
XM_005274604.2:c.1526C>A	XP_005274661.1:p.Thr509Asn
XM_005274606.2:c.1502C>A	XP_005274663.1:p.Thr501Asn
XM_005274607.3:c.1226C>A	XP_005274664.1:p.Thr409Asn
XM_011545591.1:c.1667C>A	XP_011543893.1:p.Thr556Asn
XM_011545592.1:c.1454C>A	XP_011543894.1:p.Thr485Asn
XM_011545593.1:c.1667C>A	XP_011543895.1:p.Thr556Asn
XM_011545594.1:c.1325C>A	XP_011543896.1:p.Thr442Asn
XM_011545595.1:c.1325C>A	XP_011543897.1:p.Thr442Asn
XM_011545596.1:c.1667C>A	XP_011543898.1:p.Thr556Asn
XM_011545597.1:c.1226C>A	XP_011543899.1:p.Thr409Asn
XM_011545598.1:c.371C>A	XP_011543900.1:p.Thr124Asn
XR_247288.2:n.2006C>A
NM_001330209.1:c.1526C>A	NP_001317138.1:p.Thr509Asn
NM_001330210.1:c.1226C>A	NP_001317139.1:p.Thr409Asn
XM_005274606.4:c.1502C>A	XP_005274663.1:p.Thr501Asn
XM_011545592.3:c.1454C>A	XP_011543894.1:p.Thr485Asn
XM_011545594.3:c.1325C>A	XP_011543896.1:p.Thr442Asn
XM_011545597.2:c.1226C>A	XP_011543899.1:p.Thr409Asn
XM_017029909.1:c.1226C>A	XP_016885398.1:p.Thr409Asn
XM_017029911.1:c.704C>A	XP_016885400.1:p.Thr235Asn
XM_024452468.1:c.371C>A	XP_024308236.1:p.Thr124Asn
XM_024452469.1:c.371C>A	XP_024308237.1:p.Thr124Asn
XM_024452470.1:c.371C>A	XP_024308238.1:p.Thr124Asn
XM_024452471.1:c.371C>A	XP_024308239.1:p.Thr124Asn
NM_003611.3:c.1646C>A MANE Select	NP_003602.1:p.Thr549Asn
NM_001330209.2:c.1526C>A	NP_001317138.1:p.Thr509Asn
NM_001330210.2:c.1226C>A	NP_001317139.1:p.Thr409Asn