Canonical Allele Identifier: CA2482056999
Gene: REN HGNC NCBI

Linked Data

dbSNP Id: rs1658200892

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159262_204159265dup , CM000663.2:g.204159262_204159265dup GRCh38
NC_000001.10:g.204128390_204128393dup , CM000663.1:g.204128390_204128393dup GRCh37
NC_000001.9:g.202395013_202395016dup NCBI36
NG_012122.1:g.12074_12077dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.689+135_689+138dup MANE Select ENSP00000272190.8:n.689+135_689+138dup
ENST00000638118.1:c.575+135_575+138dup ENSP00000490307.1:n.575+135_575+138dup
ENST00000272190.8:c.689+135_689+138dup ENSP00000272190.8:n.689+135_689+138dup
NM_000537.3:c.689+135_689+138dup NP_000528.1:n.689+135_689+138dup
NM_000537.4:c.689+135_689+138dup MANE Select NP_000528.1:n.689+135_689+138dup