Canonical Allele Identifier: CA1141581509
Gene: REN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159399C= , CM000663.2:g.204159399C= GRCh38
NC_000001.10:g.204128527C= , CM000663.1:g.204128527C= GRCh37
NC_000001.9:g.202395150C= NCBI36
NG_012122.1:g.11939G=

Transcript Alleles

HGVS Amino-acid change
ENST00000272190.9:c.689G= MANE Select ENSP00000272190.8:p.Arg230=
ENST00000638118.1:c.575G= ENSP00000490307.1:p.Arg192=
ENST00000272190.8:c.689G= ENSP00000272190.8:p.Arg230=
NM_000537.3:c.689G= NP_000528.1:p.Arg230=
NM_000537.4:c.689G= MANE Select NP_000528.1:p.Arg230=