Canonical Allele Identifier: CA412333401

Gene: OFD1

Linked Data

• MyVariant Identifiers: chrX:g.13754718T>C (hg19) ; chrX:g.13736599T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.13736599T>C , CM000685.2:g.13736599T>C	GRCh38
NC_000023.10:g.13754718T>C , CM000685.1:g.13754718T>C	GRCh37
NC_000023.9:g.13664639T>C	NCBI36
NG_008872.1:g.6887T>C
NG_011555.1:g.3025A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000380567.6:c.233T>C	ENSP00000369941.2:p.Val78Ala
ENST00000398395.8:c.233T>C	ENSP00000381432.5:p.Val78Ala
ENST00000464463.6:n.516T>C
ENST00000490265.6:n.151+54T>C
ENST00000682237.1:c.233T>C	ENSP00000507121.1:p.Val78Ala
ENST00000682562.1:c.233T>C	ENSP00000507874.1:p.Val78Ala
ENST00000682953.1:c.*296T>C	ENSP00000507878.1:n.*296T>C
ENST00000683055.1:c.233T>C	ENSP00000508191.1:p.Val78Ala
ENST00000683284.1:c.112-57T>C	ENSP00000507837.1:n.112-57T>C
ENST00000683427.1:c.233T>C	ENSP00000507290.1:p.Val78Ala
ENST00000683454.1:n.122T>C
ENST00000683655.1:c.233T>C	ENSP00000506770.1:p.Val78Ala
ENST00000683713.1:c.233T>C	ENSP00000507797.1:p.Val78Ala
ENST00000684401.1:n.624T>C
ENST00000684577.1:c.233T>C	ENSP00000507871.1:p.Val78Ala
ENST00000340096.11:c.233T>C MANE Select	ENSP00000344314.6:p.Val78Ala
ENST00000340096.10:c.233T>C	ENSP00000344314.6:p.Val78Ala
ENST00000380550.6:c.233T>C	ENSP00000369923.3:p.Val78Ala
ENST00000380567.5:c.-313T>C	ENSP00000369941.1:n.-313T>C
ENST00000398395.7:c.-302T>C	ENSP00000381432.4:n.-302T>C
ENST00000490265.5:n.544T>C
NM_003611.2:c.233T>C	NP_003602.1:p.Val78Ala
XM_005274599.2:c.254T>C	XP_005274656.1:p.Val85Ala
XM_005274602.2:c.254T>C	XP_005274659.1:p.Val85Ala
XM_005274603.2:c.254T>C	XP_005274660.1:p.Val85Ala
XM_005274604.2:c.233T>C	XP_005274661.1:p.Val78Ala
XM_005274606.2:c.89T>C	XP_005274663.1:p.Val30Ala
XM_011545591.1:c.254T>C	XP_011543893.1:p.Val85Ala
XM_011545592.1:c.98-57T>C	XP_011543894.1:n.98-57T>C
XM_011545593.1:c.254T>C	XP_011543895.1:p.Val85Ala
XM_011545594.1:c.-32-57T>C	XP_011543896.1:n.-32-57T>C
XM_011545595.1:c.-32-57T>C	XP_011543897.1:n.-32-57T>C
XM_011545596.1:c.254T>C	XP_011543898.1:p.Val85Ala
XM_011545597.1:c.-313T>C	XP_011543899.1:n.-313T>C
XR_247288.2:n.593T>C
NM_001330209.1:c.233T>C	NP_001317138.1:p.Val78Ala
NM_001330210.1:c.-313T>C	NP_001317139.1:n.-313T>C
XM_005274606.4:c.89T>C	XP_005274663.1:p.Val30Ala
XM_011545592.3:c.98-57T>C	XP_011543894.1:n.98-57T>C
XM_011545594.3:c.-32-57T>C	XP_011543896.1:n.-32-57T>C
XM_011545597.2:c.-313T>C	XP_011543899.1:n.-313T>C
XM_017029909.1:c.-256-57T>C	XP_016885398.1:n.-256-57T>C
XM_024452468.1:c.-1707T>C	XP_024308236.1:n.-1707T>C
XM_024452469.1:c.-1707T>C	XP_024308237.1:n.-1707T>C
XM_024452470.1:c.-1650-57T>C	XP_024308238.1:n.-1650-57T>C
XM_024452471.1:c.-1707T>C	XP_024308239.1:n.-1707T>C
NM_003611.3:c.233T>C MANE Select	NP_003602.1:p.Val78Ala
NM_001330209.2:c.233T>C	NP_001317138.1:p.Val78Ala
NM_001330210.2:c.-313T>C	NP_001317139.1:n.-313T>C