Canonical Allele Identifier: CA517048758

Gene: OPHN1

Linked Data

• gnomAD v4: X-68064011-C-T
• MyVariant Identifiers: chrX:g.67283853C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.68064011C>T , CM000685.2:g.68064011C>T	GRCh38
NC_000023.10:g.67283853C>T , CM000685.1:g.67283853C>T	GRCh37
NC_000023.9:g.67200578C>T	NCBI36
NG_008960.1:g.374447G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355520.6:c.2001G>A MANE Select	ENSP00000347710.5:p.Glu667=
ENST00000679748.1:c.1834+9141G>A	ENSP00000505800.1:n.1834+9141G>A
ENST00000679822.1:c.1834+9141G>A	ENSP00000505810.1:n.1834+9141G>A
ENST00000680592.1:n.1507G>A
ENST00000680612.1:c.1686+32859G>A	ENSP00000505365.1:n.1686+32859G>A
ENST00000681408.1:c.1896G>A	ENSP00000506619.1:p.Glu632=
ENST00000355520.5:c.2001G>A	ENSP00000347710.5:p.Glu667=
ENST00000484842.1:n.617G>A
NM_002547.2:c.2001G>A	NP_002538.1:p.Glu667=
XM_005262270.1:c.1834+9141G>A	XP_005262327.1:n.1834+9141G>A
XM_006724653.1:c.2001G>A	XP_006724716.1:p.Glu667=
XM_011530961.1:c.2001G>A	XP_011529263.1:p.Glu667=
XM_006724653.2:c.2001G>A	XP_006724716.1:p.Glu667=
NM_002547.3:c.2001G>A MANE Select	NP_002538.1:p.Glu667=