Canonical Allele Identifier: CA2482058077
Gene: REN HGNC NCBI

Linked Data

dbSNP Id: rs1658253725

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204161985_204161988dup , CM000663.2:g.204161985_204161988dup GRCh38
NC_000001.10:g.204131113_204131116dup , CM000663.1:g.204131113_204131116dup GRCh37
NC_000001.9:g.202397736_202397739dup NCBI36
NG_012122.1:g.9356_9359dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.249+31_249+34dup MANE Select ENSP00000272190.8:n.249+31_249+34dup
ENST00000638118.1:c.135+31_135+34dup ENSP00000490307.1:n.135+31_135+34dup
ENST00000272190.8:c.249+31_249+34dup ENSP00000272190.8:n.249+31_249+34dup
NM_000537.3:c.249+31_249+34dup NP_000528.1:n.249+31_249+34dup
NM_000537.4:c.249+31_249+34dup MANE Select NP_000528.1:n.249+31_249+34dup