Canonical Allele Identifier: CA2482057101
Gene: REN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159535A= , CM000663.2:g.204159535A= GRCh38
NC_000001.10:g.204128663A= , CM000663.1:g.204128663A= GRCh37
NC_000001.9:g.202395286A= NCBI36
NG_012122.1:g.11803T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.553T= MANE Select ENSP00000272190.8:p.Phe185=
ENST00000638118.1:c.439T= ENSP00000490307.1:p.Phe147=
ENST00000272190.8:c.553T= ENSP00000272190.8:p.Phe185=
NM_000537.3:c.553T= NP_000528.1:p.Phe185=
NM_000537.4:c.553T= MANE Select NP_000528.1:p.Phe185=