Canonical Allele Identifier: CA2482057094
Gene: REN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159511C= , CM000663.2:g.204159511C= GRCh38
NC_000001.10:g.204128639C= , CM000663.1:g.204128639C= GRCh37
NC_000001.9:g.202395262C= NCBI36
NG_012122.1:g.11827G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.577G= MANE Select ENSP00000272190.8:p.Val193=
ENST00000638118.1:c.463G= ENSP00000490307.1:p.Val155=
ENST00000272190.8:c.577G= ENSP00000272190.8:p.Val193=
NM_000537.3:c.577G= NP_000528.1:p.Val193=
NM_000537.4:c.577G= MANE Select NP_000528.1:p.Val193=