Canonical Allele Identifier: CA1108641968
Gene: RARRES2 HGNC NCBI

Linked Data

dbSNP Id: rs1798422513

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150339389_150339392del , CM000669.2:g.150339389_150339392del GRCh38
NC_000007.13:g.150036478_150036481del , CM000669.1:g.150036478_150036481del GRCh37
NC_000007.12:g.149667411_149667414del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000223271.8:c.280-307_280-304del MANE Select ENSP00000223271.3:n.280-307_280-304del
ENST00000223271.7:c.280-307_280-304del ENSP00000223271.3:n.280-307_280-304del
ENST00000466675.5:c.280-307_280-304del ENSP00000418009.1:n.280-307_280-304del
ENST00000467793.5:c.280-307_280-304del ENSP00000417669.1:n.280-307_280-304del
ENST00000478771.2:n.1562-307_1562-304del
ENST00000482669.1:c.280-307_280-304del ENSP00000418483.1:n.280-307_280-304del
NM_002889.3:c.280-307_280-304del NP_002880.1:n.280-307_280-304del
XM_017012491.1:c.280-307_280-304del XP_016867980.1:n.280-307_280-304del
NM_002889.4:c.280-307_280-304del MANE Select NP_002880.1:n.280-307_280-304del