Canonical Allele Identifier: CA2482058075
Gene: REN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204161978_204161980delinsCAG , CM000663.2:g.204161978_204161980delinsCAG GRCh38
NC_000001.10:g.204131106_204131108delinsCAG , CM000663.1:g.204131106_204131108delinsCAG GRCh37
NC_000001.9:g.202397729_202397731delinsCAG NCBI36
NG_012122.1:g.9358_9360delinsCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.249+33_249+35delinsCTG MANE Select ENSP00000272190.8:n.249+33_249+35delinsCTG
ENST00000638118.1:c.135+33_135+35delinsCTG ENSP00000490307.1:n.135+33_135+35delinsCTG
ENST00000272190.8:c.249+33_249+35delinsCTG ENSP00000272190.8:n.249+33_249+35delinsCTG
NM_000537.3:c.249+33_249+35delinsCTG NP_000528.1:n.249+33_249+35delinsCTG
NM_000537.4:c.249+33_249+35delinsCTG MANE Select NP_000528.1:n.249+33_249+35delinsCTG