Canonical Allele Identifier: CA344338509
Gene: REN HGNC NCBI

Linked Data

dbSNP Id: rs1457497079

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159544C>T , CM000663.2:g.204159544C>T GRCh38
NC_000001.10:g.204128672C>T , CM000663.1:g.204128672C>T GRCh37
NC_000001.9:g.202395295C>T NCBI36
NG_012122.1:g.11794G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.544G>A MANE Select ENSP00000272190.8:p.Ala182Thr
ENST00000638118.1:c.430G>A ENSP00000490307.1:p.Ala144Thr
ENST00000272190.8:c.544G>A ENSP00000272190.8:p.Ala182Thr
NM_000537.3:c.544G>A NP_000528.1:p.Ala182Thr
NM_000537.4:c.544G>A MANE Select NP_000528.1:p.Ala182Thr