Canonical Allele Identifier: CA1143958287
Gene: REN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204160559C= , CM000663.2:g.204160559C= GRCh38
NC_000001.10:g.204129687C= , CM000663.1:g.204129687C= GRCh37
NC_000001.9:g.202396310C= NCBI36
NG_012122.1:g.10779G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.492+1G= MANE Select ENSP00000272190.8:n.492+1G=
ENST00000638118.1:c.378+1G= ENSP00000490307.1:n.378+1G=
ENST00000272190.8:c.492+1G= ENSP00000272190.8:n.492+1G=
NM_000537.3:c.492+1G= NP_000528.1:n.492+1G=
NM_000537.4:c.492+1G= MANE Select NP_000528.1:n.492+1G=