Canonical Allele Identifier: CA2482059496
Gene: REN HGNC NCBI

Linked Data

dbSNP Id: rs1658326937

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204165443_204165450del , CM000663.2:g.204165443_204165450del GRCh38
NC_000001.10:g.204134571_204134578del , CM000663.1:g.204134571_204134578del GRCh37
NC_000001.9:g.202401194_202401201del NCBI36
NG_012122.1:g.5888_5895del

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.98+746_98+753del MANE Select ENSP00000272190.8:n.98+746_98+753del
ENST00000638118.1:c.-16-3287_-16-3280del ENSP00000490307.1:n.-16-3287_-16-3280del
ENST00000272190.8:c.98+746_98+753del ENSP00000272190.8:n.98+746_98+753del
NM_000537.3:c.98+746_98+753del NP_000528.1:n.98+746_98+753del
NM_000537.4:c.98+746_98+753del MANE Select NP_000528.1:n.98+746_98+753del