Canonical Allele Identifier: CA413430589

Gene: OPHN1

Linked Data

• MyVariant Identifiers: chrX:g.67283882A>C (hg19) ; chrX:g.68064040A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.68064040A>C , CM000685.2:g.68064040A>C	GRCh38
NC_000023.10:g.67283882A>C , CM000685.1:g.67283882A>C	GRCh37
NC_000023.9:g.67200607A>C	NCBI36
NG_008960.1:g.374418T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355520.6:c.1972T>G MANE Select	ENSP00000347710.5:p.Leu658Val
ENST00000679748.1:c.1834+9112T>G	ENSP00000505800.1:n.1834+9112T>G
ENST00000679822.1:c.1834+9112T>G	ENSP00000505810.1:n.1834+9112T>G
ENST00000680592.1:n.1478T>G
ENST00000680612.1:c.1686+32830T>G	ENSP00000505365.1:n.1686+32830T>G
ENST00000681408.1:c.1867T>G	ENSP00000506619.1:p.Leu623Val
ENST00000355520.5:c.1972T>G	ENSP00000347710.5:p.Leu658Val
ENST00000484842.1:n.588T>G
NM_002547.2:c.1972T>G	NP_002538.1:p.Leu658Val
XM_005262270.1:c.1834+9112T>G	XP_005262327.1:n.1834+9112T>G
XM_006724653.1:c.1972T>G	XP_006724716.1:p.Leu658Val
XM_011530961.1:c.1972T>G	XP_011529263.1:p.Leu658Val
XM_006724653.2:c.1972T>G	XP_006724716.1:p.Leu658Val
NM_002547.3:c.1972T>G MANE Select	NP_002538.1:p.Leu658Val