Canonical Allele Identifier: CA2482057104
Gene: REN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159545G= , CM000663.2:g.204159545G= GRCh38
NC_000001.10:g.204128673G= , CM000663.1:g.204128673G= GRCh37
NC_000001.9:g.202395296G= NCBI36
NG_012122.1:g.11793C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.543C= MANE Select ENSP00000272190.8:p.Pro181=
ENST00000638118.1:c.429C= ENSP00000490307.1:p.Pro143=
ENST00000272190.8:c.543C= ENSP00000272190.8:p.Pro181=
NM_000537.3:c.543C= NP_000528.1:p.Pro181=
NM_000537.4:c.543C= MANE Select NP_000528.1:p.Pro181=