Canonical Allele Identifier: CA1142178869
Gene: REN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159555G= , CM000663.2:g.204159555G= GRCh38
NC_000001.10:g.204128683G= , CM000663.1:g.204128683G= GRCh37
NC_000001.9:g.202395306G= NCBI36
NG_012122.1:g.11783C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.533C= MANE Select ENSP00000272190.8:p.Thr178=
ENST00000638118.1:c.419C= ENSP00000490307.1:p.Thr140=
ENST00000272190.8:c.533C= ENSP00000272190.8:p.Thr178=
NM_000537.3:c.533C= NP_000528.1:p.Thr178=
NM_000537.4:c.533C= MANE Select NP_000528.1:p.Thr178=
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