Canonical Allele Identifier: CA2396206928

Gene: RANBP1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20125743T= , CM000684.2:g.20125743T=	GRCh38
NC_000022.10:g.20113266T= , CM000684.1:g.20113266T=	GRCh37
NC_000022.9:g.18493266T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000331821.8:c.439+307T=	ENSP00000327583.3:n.439+307T=
ENST00000448394.3:c.*206+307T=	ENSP00000516768.1:n.*206+307T=
ENST00000430524.6:c.670+307T= MANE Select	ENSP00000401564.2:n.670+307T=
ENST00000331821.7:c.439+307T=	ENSP00000327583.3:n.439+307T=
ENST00000402752.5:c.439+307T=	ENSP00000384925.1:n.439+307T=
ENST00000418705.2:c.289+307T=	ENSP00000413502.2:n.289+307T=
ENST00000423859.5:c.289+307T=	ENSP00000404298.1:n.289+307T=
ENST00000430524.5:c.670+307T=	ENSP00000401564.2:n.670+307T=
ENST00000435265.5:c.*531+307T=	ENSP00000390139.1:n.*531+307T=
ENST00000448394.2:n.220+307T=
ENST00000486575.1:n.1298+307T=
NM_001278639.1:c.670+307T=	NP_001265568.1:n.670+307T=
NM_001278640.1:c.439+307T=	NP_001265569.1:n.439+307T=
NM_001278641.1:c.289+307T=	NP_001265570.1:n.289+307T=
NM_002882.3:c.439+307T=	NP_002873.1:n.439+307T=
XM_011530289.1:c.*131T=	XP_011528591.1:n.*131T=
XM_011530290.1:c.169+307T=	XP_011528592.1:n.169+307T=
XM_011530291.1:c.289+307T=	XP_011528593.1:n.289+307T=
XM_011530292.1:c.169+307T=	XP_011528594.1:n.169+307T=
XM_011530289.3:c.*131T=	XP_011528591.1:n.*131T=
XM_011530290.2:c.169+307T=	XP_011528592.1:n.169+307T=
XM_011530291.3:c.289+307T=	XP_011528593.1:n.289+307T=
XM_017028890.2:c.439+307T=	XP_016884379.1:n.439+307T=
XM_017028891.1:c.289+307T=	XP_016884380.1:n.289+307T=
XM_017028892.1:c.289+307T=	XP_016884381.1:n.289+307T=
NM_001278639.2:c.670+307T= MANE Select	NP_001265568.1:n.670+307T=
NM_001278640.2:c.439+307T=	NP_001265569.1:n.439+307T=
NM_001278641.2:c.289+307T=	NP_001265570.1:n.289+307T=
NM_002882.4:c.439+307T=	NP_002873.1:n.439+307T=