Canonical Allele Identifier: CA2482057141
Gene: REN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159635C= , CM000663.2:g.204159635C= GRCh38
NC_000001.10:g.204128763C= , CM000663.1:g.204128763C= GRCh37
NC_000001.9:g.202395386C= NCBI36
NG_012122.1:g.11703G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.493-40G= MANE Select ENSP00000272190.8:n.493-40G=
ENST00000638118.1:c.379-40G= ENSP00000490307.1:n.379-40G=
ENST00000272190.8:c.493-40G= ENSP00000272190.8:n.493-40G=
NM_000537.3:c.493-40G= NP_000528.1:n.493-40G=
NM_000537.4:c.493-40G= MANE Select NP_000528.1:n.493-40G=