Canonical Allele Identifier: CA2482057058
Gene: REN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159401G= , CM000663.2:g.204159401G= GRCh38
NC_000001.10:g.204128529G= , CM000663.1:g.204128529G= GRCh37
NC_000001.9:g.202395152G= NCBI36
NG_012122.1:g.11937C=

Transcript Alleles

HGVS Amino-acid change
ENST00000272190.9:c.687C= MANE Select ENSP00000272190.8:p.Asn229=
ENST00000638118.1:c.573C= ENSP00000490307.1:p.Asn191=
ENST00000272190.8:c.687C= ENSP00000272190.8:p.Asn229=
NM_000537.3:c.687C= NP_000528.1:p.Asn229=
NM_000537.4:c.687C= MANE Select NP_000528.1:p.Asn229=