Canonical Allele Identifier: CA658824641

Gene: OFD1

Linked Data

• ClinVar Variation Id: 559928
• ClinVar RCV Id: RCV000677724
• dbSNP Id: rs1555900675
• MyVariant Identifiers: chrX:g.13754595del (hg19) ; chrX:g.13736476del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.13736476del , CM000685.2:g.13736476del	GRCh38
NC_000023.10:g.13754595del , CM000685.1:g.13754595del	GRCh37
NC_000023.9:g.13664516del	NCBI36
NG_008872.1:g.6764del
NG_011555.1:g.3148del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380567.6:c.112-2del	ENSP00000369941.2:n.112-2del
ENST00000398395.8:c.112-2del	ENSP00000381432.5:n.112-2del
ENST00000464463.6:n.395-2del
ENST00000485052.6:n.605-2del
ENST00000490265.6:n.84-2del
ENST00000682237.1:c.112-2del	ENSP00000507121.1:n.112-2del
ENST00000682562.1:c.112-2del	ENSP00000507874.1:n.112-2del
ENST00000682953.1:c.*175-2del	ENSP00000507878.1:n.*175-2del
ENST00000683055.1:c.112-2del	ENSP00000508191.1:n.112-2del
ENST00000683284.1:c.112-180del	ENSP00000507837.1:n.112-180del
ENST00000683427.1:c.112-2del	ENSP00000507290.1:n.112-2del
ENST00000683655.1:c.112-2del	ENSP00000506770.1:n.112-2del
ENST00000683713.1:c.112-2del	ENSP00000507797.1:n.112-2del
ENST00000684401.1:n.501del
ENST00000684577.1:c.112-2del	ENSP00000507871.1:n.112-2del
ENST00000340096.11:c.112-2del MANE Select	ENSP00000344314.6:n.112-2del
ENST00000340096.10:c.112-2del	ENSP00000344314.6:n.112-2del
ENST00000380550.6:c.112-2del	ENSP00000369923.3:n.112-2del
ENST00000380567.5:c.-434-2del	ENSP00000369941.1:n.-434-2del
ENST00000398395.7:c.-423-2del	ENSP00000381432.4:n.-423-2del
ENST00000485052.5:n.616-2del
ENST00000490265.5:n.423-2del
NM_003611.2:c.112-2del	NP_003602.1:n.112-2del
XM_005274599.2:c.133-2del	XP_005274656.1:n.133-2del
XM_005274602.2:c.133-2del	XP_005274659.1:n.133-2del
XM_005274603.2:c.133-2del	XP_005274660.1:n.133-2del
XM_005274604.2:c.112-2del	XP_005274661.1:n.112-2del
XM_005274606.2:c.-33-2del	XP_005274663.1:n.-33-2del
XM_011545591.1:c.133-2del	XP_011543893.1:n.133-2del
XM_011545592.1:c.98-180del	XP_011543894.1:n.98-180del
XM_011545593.1:c.133-2del	XP_011543895.1:n.133-2del
XM_011545594.1:c.-32-180del	XP_011543896.1:n.-32-180del
XM_011545595.1:c.-32-180del	XP_011543897.1:n.-32-180del
XM_011545596.1:c.133-2del	XP_011543898.1:n.133-2del
XM_011545597.1:c.-434-2del	XP_011543899.1:n.-434-2del
XR_247288.2:n.472-2del
NM_001330209.1:c.112-2del	NP_001317138.1:n.112-2del
NM_001330210.1:c.-434-2del	NP_001317139.1:n.-434-2del
XM_005274606.4:c.-33-2del	XP_005274663.1:n.-33-2del
XM_011545592.3:c.98-180del	XP_011543894.1:n.98-180del
XM_011545594.3:c.-32-180del	XP_011543896.1:n.-32-180del
XM_011545597.2:c.-434-2del	XP_011543899.1:n.-434-2del
XM_017029909.1:c.-256-180del	XP_016885398.1:n.-256-180del
XM_024452468.1:c.-1828-2del	XP_024308236.1:n.-1828-2del
XM_024452469.1:c.-1828-2del	XP_024308237.1:n.-1828-2del
XM_024452470.1:c.-1650-180del	XP_024308238.1:n.-1650-180del
XM_024452471.1:c.-1828-2del	XP_024308239.1:n.-1828-2del
NM_003611.3:c.112-2del MANE Select	NP_003602.1:n.112-2del
NM_001330209.2:c.112-2del	NP_001317138.1:n.112-2del
NM_001330210.2:c.-434-2del	NP_001317139.1:n.-434-2del