Canonical Allele Identifier: CA412344352

Gene: OFD1

Linked Data

• MyVariant Identifiers: chrX:g.13778604G>C (hg19) ; chrX:g.13760485G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.13760485G>C , CM000685.2:g.13760485G>C	GRCh38
NC_000023.10:g.13778604G>C , CM000685.1:g.13778604G>C	GRCh37
NC_000023.9:g.13688525G>C	NCBI36
NG_008872.1:g.30773G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380567.6:c.*1718G>C	ENSP00000369941.2:n.*1718G>C
ENST00000398395.8:c.*1486G>C	ENSP00000381432.5:n.*1486G>C
ENST00000464463.6:n.3854G>C
ENST00000490265.6:n.2554G>C
ENST00000682237.1:c.*1585G>C	ENSP00000507121.1:n.*1585G>C
ENST00000682562.1:c.*3427G>C	ENSP00000507874.1:n.*3427G>C
ENST00000682953.1:c.*2752G>C	ENSP00000507878.1:n.*2752G>C
ENST00000683055.1:c.*3006G>C	ENSP00000508191.1:n.*3006G>C
ENST00000683284.1:c.*2256G>C	ENSP00000507837.1:n.*2256G>C
ENST00000683427.1:c.*682G>C	ENSP00000507290.1:n.*682G>C
ENST00000683454.1:n.2039G>C
ENST00000683637.1:n.3134G>C
ENST00000683655.1:c.*2239G>C	ENSP00000506770.1:n.*2239G>C
ENST00000683713.1:c.*2256G>C	ENSP00000507797.1:n.*2256G>C
ENST00000684577.1:c.*1722G>C	ENSP00000507871.1:n.*1722G>C
ENST00000340096.11:c.2025G>C MANE Select	ENSP00000344314.6:p.Leu675Phe
ENST00000340096.10:c.2025G>C	ENSP00000344314.6:p.Leu675Phe
ENST00000380550.6:c.1905G>C	ENSP00000369923.3:p.Leu635Phe
ENST00000380567.5:c.1605G>C	ENSP00000369941.1:p.Leu535Phe
ENST00000398395.7:c.*365G>C	ENSP00000381432.4:n.*365G>C
ENST00000490265.5:n.3000G>C
NM_003611.2:c.2025G>C	NP_003602.1:p.Leu675Phe
XM_005274599.2:c.2046G>C	XP_005274656.1:p.Leu682Phe
XM_005274602.2:c.2046G>C	XP_005274659.1:p.Leu682Phe
XM_005274603.2:c.1926G>C	XP_005274660.1:p.Leu642Phe
XM_005274604.2:c.1905G>C	XP_005274661.1:p.Leu635Phe
XM_005274606.2:c.1881G>C	XP_005274663.1:p.Leu627Phe
XM_005274607.3:c.1605G>C	XP_005274664.1:p.Leu535Phe
XM_011545591.1:c.2046G>C	XP_011543893.1:p.Leu682Phe
XM_011545592.1:c.1833G>C	XP_011543894.1:p.Leu611Phe
XM_011545593.1:c.2046G>C	XP_011543895.1:p.Leu682Phe
XM_011545594.1:c.1704G>C	XP_011543896.1:p.Leu568Phe
XM_011545595.1:c.1704G>C	XP_011543897.1:p.Leu568Phe
XM_011545596.1:c.2046G>C	XP_011543898.1:p.Leu682Phe
XM_011545597.1:c.1605G>C	XP_011543899.1:p.Leu535Phe
XM_011545598.1:c.750G>C	XP_011543900.1:p.Leu250Phe
XR_247288.2:n.2385G>C
NM_001330209.1:c.1905G>C	NP_001317138.1:p.Leu635Phe
NM_001330210.1:c.1605G>C	NP_001317139.1:p.Leu535Phe
XM_005274606.4:c.1881G>C	XP_005274663.1:p.Leu627Phe
XM_011545592.3:c.1833G>C	XP_011543894.1:p.Leu611Phe
XM_011545594.3:c.1704G>C	XP_011543896.1:p.Leu568Phe
XM_011545597.2:c.1605G>C	XP_011543899.1:p.Leu535Phe
XM_017029909.1:c.1605G>C	XP_016885398.1:p.Leu535Phe
XM_017029911.1:c.1083G>C	XP_016885400.1:p.Leu361Phe
XM_024452468.1:c.750G>C	XP_024308236.1:p.Leu250Phe
XM_024452469.1:c.750G>C	XP_024308237.1:p.Leu250Phe
XM_024452470.1:c.750G>C	XP_024308238.1:p.Leu250Phe
XM_024452471.1:c.750G>C	XP_024308239.1:p.Leu250Phe
NM_003611.3:c.2025G>C MANE Select	NP_003602.1:p.Leu675Phe
NM_001330209.2:c.1905G>C	NP_001317138.1:p.Leu635Phe
NM_001330210.2:c.1605G>C	NP_001317139.1:p.Leu535Phe