Canonical Allele Identifier: CA344339733
Gene: REN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204160657G>A , CM000663.2:g.204160657G>A GRCh38
NC_000001.10:g.204129785G>A , CM000663.1:g.204129785G>A GRCh37
NC_000001.9:g.202396408G>A NCBI36
NG_012122.1:g.10681C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.395C>T MANE Select ENSP00000272190.8:p.Ala132Val
ENST00000638118.1:c.281C>T ENSP00000490307.1:p.Ala94Val
ENST00000272190.8:c.395C>T ENSP00000272190.8:p.Ala132Val
NM_000537.3:c.395C>T NP_000528.1:p.Ala132Val
NM_000537.4:c.395C>T MANE Select NP_000528.1:p.Ala132Val