Canonical Allele Identifier: CA2482057015
Gene: REN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159307A= , CM000663.2:g.204159307A= GRCh38
NC_000001.10:g.204128435A= , CM000663.1:g.204128435A= GRCh37
NC_000001.9:g.202395058A= NCBI36
NG_012122.1:g.12031T=

Transcript Alleles

HGVS Amino-acid change
ENST00000272190.9:c.689+92T= MANE Select ENSP00000272190.8:n.689+92T=
ENST00000638118.1:c.575+92T= ENSP00000490307.1:n.575+92T=
ENST00000272190.8:c.689+92T= ENSP00000272190.8:n.689+92T=
NM_000537.3:c.689+92T= NP_000528.1:n.689+92T=
NM_000537.4:c.689+92T= MANE Select NP_000528.1:n.689+92T=