Canonical Allele Identifier: CA413430712

Gene: OPHN1

Linked Data

• ClinVar Variation Id: 436109
• ClinVar RCV Id: RCV000500931
• dbSNP Id: rs1555930507
• MyVariant Identifiers: chrX:g.67283908C>T (hg19) ; chrX:g.68064066C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.68064066C>T , CM000685.2:g.68064066C>T	GRCh38
NC_000023.10:g.67283908C>T , CM000685.1:g.67283908C>T	GRCh37
NC_000023.9:g.67200633C>T	NCBI36
NG_008960.1:g.374392G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355520.6:c.1946G>A MANE Select	ENSP00000347710.5:p.Gly649Glu
ENST00000679748.1:c.1834+9086G>A	ENSP00000505800.1:n.1834+9086G>A
ENST00000679822.1:c.1834+9086G>A	ENSP00000505810.1:n.1834+9086G>A
ENST00000680592.1:n.1452G>A
ENST00000680612.1:c.1686+32804G>A	ENSP00000505365.1:n.1686+32804G>A
ENST00000681408.1:c.1841G>A	ENSP00000506619.1:p.Gly614Glu
ENST00000355520.5:c.1946G>A	ENSP00000347710.5:p.Gly649Glu
ENST00000484842.1:n.562G>A
NM_002547.2:c.1946G>A	NP_002538.1:p.Gly649Glu
XM_005262270.1:c.1834+9086G>A	XP_005262327.1:n.1834+9086G>A
XM_006724653.1:c.1946G>A	XP_006724716.1:p.Gly649Glu
XM_011530961.1:c.1946G>A	XP_011529263.1:p.Gly649Glu
XM_006724653.2:c.1946G>A	XP_006724716.1:p.Gly649Glu
NM_002547.3:c.1946G>A MANE Select	NP_002538.1:p.Gly649Glu