Canonical Allele Identifier: CA1527029396

Gene: ROPN1L

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10463995C= , CM000667.2:g.10463995C=	GRCh38
NC_000005.9:g.10464107C= , CM000667.1:g.10464107C=	GRCh37
NC_000005.8:g.10517107C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274134.5:c.594-853C= MANE Select	ENSP00000274134.4:n.594-853C=
ENST00000274134.4:c.594-853C=	ENSP00000274134.4:n.594-853C=
ENST00000503804.5:c.594-853C=	ENSP00000421405.1:n.594-853C=
ENST00000510520.5:n.885+2636C=
NM_001201466.1:c.594-853C=	NP_001188395.1:n.594-853C=
NM_031916.4:c.594-853C=	NP_114122.2:n.594-853C=
XM_006714503.2:c.593+2636C=	XP_006714566.1:n.593+2636C=
XM_006714504.2:c.593+2636C=	XP_006714567.1:n.593+2636C=
XM_011514190.1:c.26C=	XP_011512492.1:p.Thr9=
XM_006714504.3:c.593+2636C=	XP_006714567.1:n.593+2636C=
XM_011514190.2:c.26C=	XP_011512492.1:p.Thr9=
XM_017009946.2:c.593+2636C=	XP_016865435.1:n.593+2636C=
XM_017009947.2:c.593+2636C=	XP_016865436.1:n.593+2636C=
NM_031916.5:c.594-853C= MANE Select	NP_114122.2:n.594-853C=
NM_001201466.2:c.594-853C=	NP_001188395.1:n.594-853C=