Canonical Allele Identifier: CA2482057130
Gene: REN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159613A= , CM000663.2:g.204159613A= GRCh38
NC_000001.10:g.204128741A= , CM000663.1:g.204128741A= GRCh37
NC_000001.9:g.202395364A= NCBI36
NG_012122.1:g.11725T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.493-18T= MANE Select ENSP00000272190.8:n.493-18T=
ENST00000638118.1:c.379-18T= ENSP00000490307.1:n.379-18T=
ENST00000272190.8:c.493-18T= ENSP00000272190.8:n.493-18T=
NM_000537.3:c.493-18T= NP_000528.1:n.493-18T=
NM_000537.4:c.493-18T= MANE Select NP_000528.1:n.493-18T=