Canonical Allele Identifier: CA2482059403
Gene: REN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204165224_204165225delinsGC , CM000663.2:g.204165224_204165225delinsGC GRCh38
NC_000001.10:g.204134352_204134353delinsGC , CM000663.1:g.204134352_204134353delinsGC GRCh37
NC_000001.9:g.202400975_202400976delinsGC NCBI36
NG_012122.1:g.6113_6114delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.98+971_98+972delinsGC MANE Select ENSP00000272190.8:n.98+971_98+972delinsGC
ENST00000638118.1:c.-16-3062_-16-3061delinsGC ENSP00000490307.1:n.-16-3062_-16-3061delinsGC
ENST00000272190.8:c.98+971_98+972delinsGC ENSP00000272190.8:n.98+971_98+972delinsGC
NM_000537.3:c.98+971_98+972delinsGC NP_000528.1:n.98+971_98+972delinsGC
NM_000537.4:c.98+971_98+972delinsGC MANE Select NP_000528.1:n.98+971_98+972delinsGC