Canonical Allele Identifier: CA2482059435
Gene: REN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204165300T= , CM000663.2:g.204165300T= GRCh38
NC_000001.10:g.204134428T= , CM000663.1:g.204134428T= GRCh37
NC_000001.9:g.202401051T= NCBI36
NG_012122.1:g.6038A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.98+896A= MANE Select ENSP00000272190.8:n.98+896A=
ENST00000638118.1:c.-16-3137A= ENSP00000490307.1:n.-16-3137A=
ENST00000272190.8:c.98+896A= ENSP00000272190.8:n.98+896A=
NM_000537.3:c.98+896A= NP_000528.1:n.98+896A=
NM_000537.4:c.98+896A= MANE Select NP_000528.1:n.98+896A=