Canonical Allele Identifier: CA516984474

Gene: OPHN1

Linked Data

• MyVariant Identifiers: chrX:g.67518850A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.68299008A>T , CM000685.2:g.68299008A>T	GRCh38
NC_000023.10:g.67518850A>T , CM000685.1:g.67518850A>T	GRCh37
NC_000023.9:g.67435575A>T	NCBI36
NG_008960.1:g.139450T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000355520.6:c.243T>A MANE Select	ENSP00000347710.5:p.Ile81=
ENST00000679748.1:c.243T>A	ENSP00000505800.1:p.Ile81=
ENST00000679822.1:c.243T>A	ENSP00000505810.1:p.Ile81=
ENST00000679914.1:n.602T>A
ENST00000680417.1:n.64T>A
ENST00000680503.1:n.920T>A
ENST00000680612.1:c.243T>A	ENSP00000505365.1:p.Ile81=
ENST00000681408.1:c.243T>A	ENSP00000506619.1:p.Ile81=
ENST00000355520.5:c.243T>A	ENSP00000347710.5:p.Ile81=
ENST00000486068.1:n.113T>A
NM_002547.2:c.243T>A	NP_002538.1:p.Ile81=
XM_005262270.1:c.243T>A	XP_005262327.1:p.Ile81=
XM_006724653.1:c.243T>A	XP_006724716.1:p.Ile81=
XM_011530961.1:c.243T>A	XP_011529263.1:p.Ile81=
XM_006724653.2:c.243T>A	XP_006724716.1:p.Ile81=
XM_017029555.1:c.243T>A	XP_016885044.1:p.Ile81=
NM_002547.3:c.243T>A MANE Select	NP_002538.1:p.Ile81=