Canonical Allele Identifier: CA2396203720

Gene: RANBP1

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20120206G>T , CM000684.2:g.20120206G>T	GRCh38
NC_000022.10:g.20107729G>T , CM000684.1:g.20107729G>T	GRCh37
NC_000022.9:g.18487729G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331821.8:c.152+1057G>T	ENSP00000327583.3:n.152+1057G>T
ENST00000411892.6:n.245+1057G>T
ENST00000448394.3:c.152+1057G>T	ENSP00000516768.1:n.152+1057G>T
ENST00000430524.6:c.383+1057G>T MANE Select	ENSP00000401564.2:n.383+1057G>T
ENST00000331821.7:c.152+1057G>T	ENSP00000327583.3:n.152+1057G>T
ENST00000402752.5:c.152+1057G>T	ENSP00000384925.1:n.152+1057G>T
ENST00000411892.5:c.152+1057G>T	ENSP00000395472.1:n.152+1057G>T
ENST00000416427.5:c.2+1057G>T	ENSP00000404126.1:n.2+1057G>T
ENST00000418705.2:c.2+1057G>T	ENSP00000413502.2:n.2+1057G>T
ENST00000421656.5:c.2+1057G>T	ENSP00000400940.1:n.2+1057G>T
ENST00000423859.5:c.2+1057G>T	ENSP00000404298.1:n.2+1057G>T
ENST00000430524.5:c.383+1057G>T	ENSP00000401564.2:n.383+1057G>T
ENST00000432879.5:c.383+1057G>T	ENSP00000404724.1:n.383+1057G>T
ENST00000435265.5:c.*126+1057G>T	ENSP00000390139.1:n.*126+1057G>T
ENST00000488484.1:n.278+1057G>T
NM_001278639.1:c.383+1057G>T	NP_001265568.1:n.383+1057G>T
NM_001278640.1:c.152+1057G>T	NP_001265569.1:n.152+1057G>T
NM_001278641.1:c.2+1057G>T	NP_001265570.1:n.2+1057G>T
NM_002882.3:c.152+1057G>T	NP_002873.1:n.152+1057G>T
XM_011530289.1:c.152+1057G>T	XP_011528591.1:n.152+1057G>T
XM_011530291.1:c.2+1057G>T	XP_011528593.1:n.2+1057G>T
XM_011530289.3:c.152+1057G>T	XP_011528591.1:n.152+1057G>T
XM_011530290.2:c.-395+1057G>T	XP_011528592.1:n.-395+1057G>T
XM_011530291.3:c.2+1057G>T	XP_011528593.1:n.2+1057G>T
XM_017028890.2:c.152+1057G>T	XP_016884379.1:n.152+1057G>T
XM_017028891.1:c.2+1057G>T	XP_016884380.1:n.2+1057G>T
XM_017028892.1:c.2+1057G>T	XP_016884381.1:n.2+1057G>T
NM_001278639.2:c.383+1057G>T MANE Select	NP_001265568.1:n.383+1057G>T
NM_001278640.2:c.152+1057G>T	NP_001265569.1:n.152+1057G>T
NM_001278641.2:c.2+1057G>T	NP_001265570.1:n.2+1057G>T
NM_002882.4:c.152+1057G>T	NP_002873.1:n.152+1057G>T