Canonical Allele Identifier: CA1141821412
Gene: REN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159458G= , CM000663.2:g.204159458G= GRCh38
NC_000001.10:g.204128586G= , CM000663.1:g.204128586G= GRCh37
NC_000001.9:g.202395209G= NCBI36
NG_012122.1:g.11880C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.630C= MANE Select ENSP00000272190.8:p.Phe210=
ENST00000638118.1:c.516C= ENSP00000490307.1:p.Phe172=
ENST00000272190.8:c.630C= ENSP00000272190.8:p.Phe210=
NM_000537.3:c.630C= NP_000528.1:p.Phe210=
NM_000537.4:c.630C= MANE Select NP_000528.1:p.Phe210=
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