Canonical Allele Identifier: CA412343491

Gene: OFD1

Linked Data

• MyVariant Identifiers: chrX:g.13776557A>C (hg19) ; chrX:g.13758438A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.13758438A>C , CM000685.2:g.13758438A>C	GRCh38
NC_000023.10:g.13776557A>C , CM000685.1:g.13776557A>C	GRCh37
NC_000023.9:g.13686478A>C	NCBI36
NG_008872.1:g.28726A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380567.6:c.*1337A>C	ENSP00000369941.2:n.*1337A>C
ENST00000398395.8:c.*1115+648A>C	ENSP00000381432.5:n.*1115+648A>C
ENST00000464463.6:n.1807A>C
ENST00000490265.6:n.2173A>C
ENST00000682237.1:c.*1204A>C	ENSP00000507121.1:n.*1204A>C
ENST00000682562.1:c.*3046A>C	ENSP00000507874.1:n.*3046A>C
ENST00000682953.1:c.*2371A>C	ENSP00000507878.1:n.*2371A>C
ENST00000683055.1:c.*959A>C	ENSP00000508191.1:n.*959A>C
ENST00000683284.1:c.*1875A>C	ENSP00000507837.1:n.*1875A>C
ENST00000683427.1:c.*311+648A>C	ENSP00000507290.1:n.*311+648A>C
ENST00000683454.1:n.1658A>C
ENST00000683637.1:n.2753A>C
ENST00000683655.1:c.*1858A>C	ENSP00000506770.1:n.*1858A>C
ENST00000683713.1:c.*1875A>C	ENSP00000507797.1:n.*1875A>C
ENST00000684577.1:c.*1341A>C	ENSP00000507871.1:n.*1341A>C
ENST00000340096.11:c.1644A>C MANE Select	ENSP00000344314.6:p.Gln548His
ENST00000340096.10:c.1644A>C	ENSP00000344314.6:p.Gln548His
ENST00000380550.6:c.1524A>C	ENSP00000369923.3:p.Gln508His
ENST00000380567.5:c.1224A>C	ENSP00000369941.1:p.Gln408His
ENST00000398395.7:c.1011+648A>C	ENSP00000381432.4:n.1011+648A>C
ENST00000490265.5:n.2619A>C
NM_003611.2:c.1644A>C	NP_003602.1:p.Gln548His
XM_005274599.2:c.1665A>C	XP_005274656.1:p.Gln555His
XM_005274602.2:c.1665A>C	XP_005274659.1:p.Gln555His
XM_005274603.2:c.1545A>C	XP_005274660.1:p.Gln515His
XM_005274604.2:c.1524A>C	XP_005274661.1:p.Gln508His
XM_005274606.2:c.1500A>C	XP_005274663.1:p.Gln500His
XM_005274607.3:c.1224A>C	XP_005274664.1:p.Gln408His
XM_011545591.1:c.1665A>C	XP_011543893.1:p.Gln555His
XM_011545592.1:c.1452A>C	XP_011543894.1:p.Gln484His
XM_011545593.1:c.1665A>C	XP_011543895.1:p.Gln555His
XM_011545594.1:c.1323A>C	XP_011543896.1:p.Gln441His
XM_011545595.1:c.1323A>C	XP_011543897.1:p.Gln441His
XM_011545596.1:c.1665A>C	XP_011543898.1:p.Gln555His
XM_011545597.1:c.1224A>C	XP_011543899.1:p.Gln408His
XM_011545598.1:c.369A>C	XP_011543900.1:p.Gln123His
XR_247288.2:n.2004A>C
NM_001330209.1:c.1524A>C	NP_001317138.1:p.Gln508His
NM_001330210.1:c.1224A>C	NP_001317139.1:p.Gln408His
XM_005274606.4:c.1500A>C	XP_005274663.1:p.Gln500His
XM_011545592.3:c.1452A>C	XP_011543894.1:p.Gln484His
XM_011545594.3:c.1323A>C	XP_011543896.1:p.Gln441His
XM_011545597.2:c.1224A>C	XP_011543899.1:p.Gln408His
XM_017029909.1:c.1224A>C	XP_016885398.1:p.Gln408His
XM_017029911.1:c.702A>C	XP_016885400.1:p.Gln234His
XM_024452468.1:c.369A>C	XP_024308236.1:p.Gln123His
XM_024452469.1:c.369A>C	XP_024308237.1:p.Gln123His
XM_024452470.1:c.369A>C	XP_024308238.1:p.Gln123His
XM_024452471.1:c.369A>C	XP_024308239.1:p.Gln123His
NM_003611.3:c.1644A>C MANE Select	NP_003602.1:p.Gln548His
NM_001330209.2:c.1524A>C	NP_001317138.1:p.Gln508His
NM_001330210.2:c.1224A>C	NP_001317139.1:p.Gln408His