Canonical Allele Identifier: CA517048492

Gene: OPHN1

Linked Data

• MyVariant Identifiers: chrX:g.67283732T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.68063890T>G , CM000685.2:g.68063890T>G	GRCh38
NC_000023.10:g.67283732T>G , CM000685.1:g.67283732T>G	GRCh37
NC_000023.9:g.67200457T>G	NCBI36
NG_008960.1:g.374568A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355520.6:c.2122A>C MANE Select	ENSP00000347710.5:p.Arg708=
ENST00000679748.1:c.1834+9262A>C	ENSP00000505800.1:n.1834+9262A>C
ENST00000679822.1:c.1834+9262A>C	ENSP00000505810.1:n.1834+9262A>C
ENST00000680592.1:n.1628A>C
ENST00000680612.1:c.1686+32980A>C	ENSP00000505365.1:n.1686+32980A>C
ENST00000681408.1:c.2017A>C	ENSP00000506619.1:p.Arg673=
ENST00000355520.5:c.2122A>C	ENSP00000347710.5:p.Arg708=
ENST00000484842.1:n.738A>C
NM_002547.2:c.2122A>C	NP_002538.1:p.Arg708=
XM_005262270.1:c.1834+9262A>C	XP_005262327.1:n.1834+9262A>C
XM_006724653.1:c.2122A>C	XP_006724716.1:p.Arg708=
XM_011530961.1:c.2122A>C	XP_011529263.1:p.Arg708=
XM_006724653.2:c.2122A>C	XP_006724716.1:p.Arg708=
NM_002547.3:c.2122A>C MANE Select	NP_002538.1:p.Arg708=