Canonical Allele Identifier: CA1141581508
Gene: REN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204155078G= , CM000663.2:g.204155078G= GRCh38
NC_000001.10:g.204124206G= , CM000663.1:g.204124206G= GRCh37
NC_000001.9:g.202390829G= NCBI36
NG_012122.1:g.16260C=

Transcript Alleles

HGVS Amino-acid change
ENST00000272190.9:c.1159C= MANE Select ENSP00000272190.8:p.Arg387=
ENST00000638118.1:c.1045C= ENSP00000490307.1:p.Arg349=
ENST00000272190.8:c.1159C= ENSP00000272190.8:p.Arg387=
NM_000537.3:c.1159C= NP_000528.1:p.Arg387=
NM_000537.4:c.1159C= MANE Select NP_000528.1:p.Arg387=