Canonical Allele Identifier: CA2435369157

Gene: OPHN1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.68298879G= , CM000685.2:g.68298879G=	GRCh38
NC_000023.10:g.67518721G= , CM000685.1:g.67518721G=	GRCh37
NC_000023.9:g.67435446G=	NCBI36
NG_008960.1:g.139579C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355520.6:c.250+122C= MANE Select	ENSP00000347710.5:n.250+122C=
ENST00000679748.1:c.250+122C=	ENSP00000505800.1:n.250+122C=
ENST00000679822.1:c.250+122C=	ENSP00000505810.1:n.250+122C=
ENST00000679914.1:n.609+122C=
ENST00000680417.1:n.71+122C=
ENST00000680503.1:n.927+122C=
ENST00000680612.1:c.250+122C=	ENSP00000505365.1:n.250+122C=
ENST00000681408.1:c.250+122C=	ENSP00000506619.1:n.250+122C=
ENST00000355520.5:c.250+122C=	ENSP00000347710.5:n.250+122C=
NM_002547.2:c.250+122C=	NP_002538.1:n.250+122C=
XM_005262270.1:c.250+122C=	XP_005262327.1:n.250+122C=
XM_006724653.1:c.250+122C=	XP_006724716.1:n.250+122C=
XM_011530961.1:c.250+122C=	XP_011529263.1:n.250+122C=
XM_006724653.2:c.250+122C=	XP_006724716.1:n.250+122C=
XM_017029555.1:c.250+122C=	XP_016885044.1:n.250+122C=
NM_002547.3:c.250+122C= MANE Select	NP_002538.1:n.250+122C=