Canonical Allele Identifier: CA1144179619
Gene: REN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204161995G= , CM000663.2:g.204161995G= GRCh38
NC_000001.10:g.204131123G= , CM000663.1:g.204131123G= GRCh37
NC_000001.9:g.202397746G= NCBI36
NG_012122.1:g.9343C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.249+18C= MANE Select ENSP00000272190.8:n.249+18C=
ENST00000638118.1:c.135+18C= ENSP00000490307.1:n.135+18C=
ENST00000272190.8:c.249+18C= ENSP00000272190.8:n.249+18C=
NM_000537.3:c.249+18C= NP_000528.1:n.249+18C=
NM_000537.4:c.249+18C= MANE Select NP_000528.1:n.249+18C=