Canonical Allele Identifier: CA1011400197
Gene: REN HGNC NCBI

Linked Data

dbSNP Id: rs1658208360

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159610del , CM000663.2:g.204159610del GRCh38
NC_000001.10:g.204128738del , CM000663.1:g.204128738del GRCh37
NC_000001.9:g.202395361del NCBI36
NG_012122.1:g.11728del

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.493-15del MANE Select ENSP00000272190.8:n.493-15del
ENST00000638118.1:c.379-15del ENSP00000490307.1:n.379-15del
ENST00000272190.8:c.493-15del ENSP00000272190.8:n.493-15del
NM_000537.3:c.493-15del NP_000528.1:n.493-15del
NM_000537.4:c.493-15del MANE Select NP_000528.1:n.493-15del