Canonical Allele Identifier: CA2482059476
Gene: REN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204165399G= , CM000663.2:g.204165399G= GRCh38
NC_000001.10:g.204134527G= , CM000663.1:g.204134527G= GRCh37
NC_000001.9:g.202401150G= NCBI36
NG_012122.1:g.5939C=

Transcript Alleles

HGVS Amino-acid change
ENST00000272190.9:c.98+797C= MANE Select ENSP00000272190.8:n.98+797C=
ENST00000638118.1:c.-16-3236C= ENSP00000490307.1:n.-16-3236C=
ENST00000272190.8:c.98+797C= ENSP00000272190.8:n.98+797C=
NM_000537.3:c.98+797C= NP_000528.1:n.98+797C=
NM_000537.4:c.98+797C= MANE Select NP_000528.1:n.98+797C=