Canonical Allele Identifier: CA344338715
Gene: REN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159577T>A , CM000663.2:g.204159577T>A GRCh38
NC_000001.10:g.204128705T>A , CM000663.1:g.204128705T>A GRCh37
NC_000001.9:g.202395328T>A NCBI36
NG_012122.1:g.11761A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.511A>T MANE Select ENSP00000272190.8:p.Thr171Ser
ENST00000638118.1:c.397A>T ENSP00000490307.1:p.Thr133Ser
ENST00000272190.8:c.511A>T ENSP00000272190.8:p.Thr171Ser
NM_000537.3:c.511A>T NP_000528.1:p.Thr171Ser
NM_000537.4:c.511A>T MANE Select NP_000528.1:p.Thr171Ser