Canonical Allele Identifier: CA1143782686
Gene: REN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159515A= , CM000663.2:g.204159515A= GRCh38
NC_000001.10:g.204128643A= , CM000663.1:g.204128643A= GRCh37
NC_000001.9:g.202395266A= NCBI36
NG_012122.1:g.11823T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.573T= MANE Select ENSP00000272190.8:p.Asp191=
ENST00000638118.1:c.459T= ENSP00000490307.1:p.Asp153=
ENST00000272190.8:c.573T= ENSP00000272190.8:p.Asp191=
NM_000537.3:c.573T= NP_000528.1:p.Asp191=
NM_000537.4:c.573T= MANE Select NP_000528.1:p.Asp191=