Canonical Allele Identifier: CA517048813

Gene: OPHN1

Linked Data

• MyVariant Identifiers: chrX:g.67283886A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.68064044A>G , CM000685.2:g.68064044A>G	GRCh38
NC_000023.10:g.67283886A>G , CM000685.1:g.67283886A>G	GRCh37
NC_000023.9:g.67200611A>G	NCBI36
NG_008960.1:g.374414T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355520.6:c.1968T>C MANE Select	ENSP00000347710.5:p.Pro656=
ENST00000679748.1:c.1834+9108T>C	ENSP00000505800.1:n.1834+9108T>C
ENST00000679822.1:c.1834+9108T>C	ENSP00000505810.1:n.1834+9108T>C
ENST00000680592.1:n.1474T>C
ENST00000680612.1:c.1686+32826T>C	ENSP00000505365.1:n.1686+32826T>C
ENST00000681408.1:c.1863T>C	ENSP00000506619.1:p.Pro621=
ENST00000355520.5:c.1968T>C	ENSP00000347710.5:p.Pro656=
ENST00000484842.1:n.584T>C
NM_002547.2:c.1968T>C	NP_002538.1:p.Pro656=
XM_005262270.1:c.1834+9108T>C	XP_005262327.1:n.1834+9108T>C
XM_006724653.1:c.1968T>C	XP_006724716.1:p.Pro656=
XM_011530961.1:c.1968T>C	XP_011529263.1:p.Pro656=
XM_006724653.2:c.1968T>C	XP_006724716.1:p.Pro656=
NM_002547.3:c.1968T>C MANE Select	NP_002538.1:p.Pro656=