Canonical Allele Identifier: CA2482059533
Gene: REN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204165543C= , CM000663.2:g.204165543C= GRCh38
NC_000001.10:g.204134671C= , CM000663.1:g.204134671C= GRCh37
NC_000001.9:g.202401294C= NCBI36
NG_012122.1:g.5795G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.98+653G= MANE Select ENSP00000272190.8:n.98+653G=
ENST00000638118.1:c.-16-3380G= ENSP00000490307.1:n.-16-3380G=
ENST00000272190.8:c.98+653G= ENSP00000272190.8:n.98+653G=
NM_000537.3:c.98+653G= NP_000528.1:n.98+653G=
NM_000537.4:c.98+653G= MANE Select NP_000528.1:n.98+653G=