Canonical Allele Identifier: CA1148870460
Gene: REN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204162118T= , CM000663.2:g.204162118T= GRCh38
NC_000001.10:g.204131246T= , CM000663.1:g.204131246T= GRCh37
NC_000001.9:g.202397869T= NCBI36
NG_012122.1:g.9220A=

Transcript Alleles

HGVS Amino-acid change
ENST00000272190.9:c.144A= MANE Select ENSP00000272190.8:p.Glu48=
ENST00000638118.1:c.30A= ENSP00000490307.1:p.Glu10=
ENST00000272190.8:c.144A= ENSP00000272190.8:p.Glu48=
NM_000537.3:c.144A= NP_000528.1:p.Glu48=
NM_000537.4:c.144A= MANE Select NP_000528.1:p.Glu48=