Canonical Allele Identifier: CA412344897

Gene: OFD1

Linked Data

• MyVariant Identifiers: chrX:g.13779218C>G (hg19) ; chrX:g.13761099C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.13761099C>G , CM000685.2:g.13761099C>G	GRCh38
NC_000023.10:g.13779218C>G , CM000685.1:g.13779218C>G	GRCh37
NC_000023.9:g.13689139C>G	NCBI36
NG_008872.1:g.31387C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380567.6:c.*1968C>G	ENSP00000369941.2:n.*1968C>G
ENST00000398395.8:c.*1736C>G	ENSP00000381432.5:n.*1736C>G
ENST00000464463.6:n.4104C>G
ENST00000490265.6:n.2804C>G
ENST00000682237.1:c.*1835C>G	ENSP00000507121.1:n.*1835C>G
ENST00000682562.1:c.*3677C>G	ENSP00000507874.1:n.*3677C>G
ENST00000682953.1:c.*3002C>G	ENSP00000507878.1:n.*3002C>G
ENST00000683055.1:c.*3256C>G	ENSP00000508191.1:n.*3256C>G
ENST00000683284.1:c.*2506C>G	ENSP00000507837.1:n.*2506C>G
ENST00000683427.1:c.*932C>G	ENSP00000507290.1:n.*932C>G
ENST00000683454.1:n.2289C>G
ENST00000683637.1:n.3384C>G
ENST00000683655.1:c.*2489C>G	ENSP00000506770.1:n.*2489C>G
ENST00000683713.1:c.*2506C>G	ENSP00000507797.1:n.*2506C>G
ENST00000684577.1:c.*1972C>G	ENSP00000507871.1:n.*1972C>G
ENST00000340096.11:c.2275C>G MANE Select	ENSP00000344314.6:p.His759Asp
ENST00000340096.10:c.2275C>G	ENSP00000344314.6:p.His759Asp
ENST00000380550.6:c.2155C>G	ENSP00000369923.3:p.His719Asp
ENST00000380567.5:c.1855C>G	ENSP00000369941.1:p.His619Asp
ENST00000398395.7:c.*615C>G	ENSP00000381432.4:n.*615C>G
ENST00000464463.5:n.96C>G
ENST00000490265.5:n.3250C>G
NM_003611.2:c.2275C>G	NP_003602.1:p.His759Asp
XM_005274599.2:c.2296C>G	XP_005274656.1:p.His766Asp
XM_005274602.2:c.2296C>G	XP_005274659.1:p.His766Asp
XM_005274603.2:c.2176C>G	XP_005274660.1:p.His726Asp
XM_005274604.2:c.2155C>G	XP_005274661.1:p.His719Asp
XM_005274606.2:c.2131C>G	XP_005274663.1:p.His711Asp
XM_005274607.3:c.1855C>G	XP_005274664.1:p.His619Asp
XM_011545591.1:c.2296C>G	XP_011543893.1:p.His766Asp
XM_011545592.1:c.2083C>G	XP_011543894.1:p.His695Asp
XM_011545593.1:c.2296C>G	XP_011543895.1:p.His766Asp
XM_011545594.1:c.1954C>G	XP_011543896.1:p.His652Asp
XM_011545595.1:c.1954C>G	XP_011543897.1:p.His652Asp
XM_011545596.1:c.2296C>G	XP_011543898.1:p.His766Asp
XM_011545597.1:c.1855C>G	XP_011543899.1:p.His619Asp
XM_011545598.1:c.1000C>G	XP_011543900.1:p.His334Asp
XR_247288.2:n.2635C>G
NM_001330209.1:c.2155C>G	NP_001317138.1:p.His719Asp
NM_001330210.1:c.1855C>G	NP_001317139.1:p.His619Asp
XM_005274606.4:c.2131C>G	XP_005274663.1:p.His711Asp
XM_011545592.3:c.2083C>G	XP_011543894.1:p.His695Asp
XM_011545594.3:c.1954C>G	XP_011543896.1:p.His652Asp
XM_011545597.2:c.1855C>G	XP_011543899.1:p.His619Asp
XM_017029909.1:c.1855C>G	XP_016885398.1:p.His619Asp
XM_017029911.1:c.1333C>G	XP_016885400.1:p.His445Asp
XM_024452468.1:c.1000C>G	XP_024308236.1:p.His334Asp
XM_024452469.1:c.1000C>G	XP_024308237.1:p.His334Asp
XM_024452470.1:c.1000C>G	XP_024308238.1:p.His334Asp
XM_024452471.1:c.1000C>G	XP_024308239.1:p.His334Asp
NM_003611.3:c.2275C>G MANE Select	NP_003602.1:p.His759Asp
NM_001330209.2:c.2155C>G	NP_001317138.1:p.His719Asp
NM_001330210.2:c.1855C>G	NP_001317139.1:p.His619Asp