Canonical Allele Identifier: CA2482057074
Gene: REN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159459_204159461delinsAAG , CM000663.2:g.204159459_204159461delinsAAG GRCh38
NC_000001.10:g.204128587_204128589delinsAAG , CM000663.1:g.204128587_204128589delinsAAG GRCh37
NC_000001.9:g.202395210_202395212delinsAAG NCBI36
NG_012122.1:g.11877_11879delinsCTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.627_629delinsCTT MANE Select ENSP00000272190.8:p.Ile209=
ENST00000638118.1:c.513_515delinsCTT ENSP00000490307.1:p.Ile171=
ENST00000272190.8:c.627_629delinsCTT ENSP00000272190.8:p.Ile209=
NM_000537.3:c.627_629delinsCTT NP_000528.1:p.Ile209=
NM_000537.4:c.627_629delinsCTT MANE Select NP_000528.1:p.Ile209=
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