Canonical Allele Identifier: CA1344844
Gene: REN HGNC NCBI

Linked Data

dbSNP Id: rs749416921

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159301_204159310del , CM000663.2:g.204159301_204159310del GRCh38
NC_000001.10:g.204128429_204128438del , CM000663.1:g.204128429_204128438del GRCh37
NC_000001.9:g.202395052_202395061del NCBI36
NG_012122.1:g.12030_12039del

Transcript Alleles

HGVS Amino-acid change
ENST00000272190.9:c.689+91_689+100del MANE Select ENSP00000272190.8:n.689+91_689+100del
ENST00000638118.1:c.575+91_575+100del ENSP00000490307.1:n.575+91_575+100del
ENST00000272190.8:c.689+91_689+100del ENSP00000272190.8:n.689+91_689+100del
NM_000537.3:c.689+91_689+100del NP_000528.1:n.689+91_689+100del
NM_000537.4:c.689+91_689+100del MANE Select NP_000528.1:n.689+91_689+100del