Canonical Allele Identifier: CA1145535932
Gene: REN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159466G= , CM000663.2:g.204159466G= GRCh38
NC_000001.10:g.204128594G= , CM000663.1:g.204128594G= GRCh37
NC_000001.9:g.202395217G= NCBI36
NG_012122.1:g.11872C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.622C= MANE Select ENSP00000272190.8:p.Pro208=
ENST00000638118.1:c.508C= ENSP00000490307.1:p.Pro170=
ENST00000272190.8:c.622C= ENSP00000272190.8:p.Pro208=
NM_000537.3:c.622C= NP_000528.1:p.Pro208=
NM_000537.4:c.622C= MANE Select NP_000528.1:p.Pro208=