Canonical Allele Identifier: CA2482059478
Gene: REN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204165404T= , CM000663.2:g.204165404T= GRCh38
NC_000001.10:g.204134532T= , CM000663.1:g.204134532T= GRCh37
NC_000001.9:g.202401155T= NCBI36
NG_012122.1:g.5934A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.98+792A= MANE Select ENSP00000272190.8:n.98+792A=
ENST00000638118.1:c.-16-3241A= ENSP00000490307.1:n.-16-3241A=
ENST00000272190.8:c.98+792A= ENSP00000272190.8:n.98+792A=
NM_000537.3:c.98+792A= NP_000528.1:n.98+792A=
NM_000537.4:c.98+792A= MANE Select NP_000528.1:n.98+792A=