Canonical Allele Identifier: CA344338053
Gene: REN HGNC NCBI

Linked Data

dbSNP Id: rs1165076402
MyVariant Identifiers: chr1:g.204128610del (hg19) chr1:g.204159483del (hg38) chr1:g.204159482del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159483del , CM000663.2:g.204159483del GRCh38
NC_000001.10:g.204128611del , CM000663.1:g.204128611del GRCh37
NC_000001.9:g.202395234del NCBI36
NG_012122.1:g.11856del

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.606del MANE Select ENSP00000272190.8:p.Ile203LeufsTer17
ENST00000638118.1:c.492del ENSP00000490307.1:p.Ile165LeufsTer17
ENST00000272190.8:c.606del ENSP00000272190.8:p.Ile203LeufsTer17
NM_000537.3:c.606del NP_000528.1:p.Ile203LeufsTer17
NM_000537.4:c.606del MANE Select NP_000528.1:p.Ile203LeufsTer17
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