Canonical Allele Identifier: CA2697919016
Gene: REN HGNC NCBI

Linked Data

dbSNP Id: rs2102312796
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159500del , CM000663.2:g.204159500del GRCh38
NC_000001.10:g.204128628del , CM000663.1:g.204128628del GRCh37
NC_000001.9:g.202395251del NCBI36
NG_012122.1:g.11840del

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.590del MANE Select ENSP00000272190.8:p.Gly197AlafsTer23
ENST00000638118.1:c.476del ENSP00000490307.1:p.Gly159AlafsTer23
ENST00000272190.8:c.590del ENSP00000272190.8:p.Gly197AlafsTer23
NM_000537.3:c.590del NP_000528.1:p.Gly197AlafsTer23
NM_000537.4:c.590del MANE Select NP_000528.1:p.Gly197AlafsTer23
Search 100 bp 5'
Search 100 bp 3'