Canonical Allele Identifier: CA2435369155

Gene: OPHN1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.68298874C= , CM000685.2:g.68298874C=	GRCh38
NC_000023.10:g.67518716C= , CM000685.1:g.67518716C=	GRCh37
NC_000023.9:g.67435441C=	NCBI36
NG_008960.1:g.139584G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355520.6:c.250+127G= MANE Select	ENSP00000347710.5:n.250+127G=
ENST00000679748.1:c.250+127G=	ENSP00000505800.1:n.250+127G=
ENST00000679822.1:c.250+127G=	ENSP00000505810.1:n.250+127G=
ENST00000679914.1:n.609+127G=
ENST00000680417.1:n.71+127G=
ENST00000680503.1:n.927+127G=
ENST00000680612.1:c.250+127G=	ENSP00000505365.1:n.250+127G=
ENST00000681408.1:c.250+127G=	ENSP00000506619.1:n.250+127G=
ENST00000355520.5:c.250+127G=	ENSP00000347710.5:n.250+127G=
NM_002547.2:c.250+127G=	NP_002538.1:n.250+127G=
XM_005262270.1:c.250+127G=	XP_005262327.1:n.250+127G=
XM_006724653.1:c.250+127G=	XP_006724716.1:n.250+127G=
XM_011530961.1:c.250+127G=	XP_011529263.1:n.250+127G=
XM_006724653.2:c.250+127G=	XP_006724716.1:n.250+127G=
XM_017029555.1:c.250+127G=	XP_016885044.1:n.250+127G=
NM_002547.3:c.250+127G= MANE Select	NP_002538.1:n.250+127G=