Canonical Allele Identifier: CA2482057113
Gene: REN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159581C= , CM000663.2:g.204159581C= GRCh38
NC_000001.10:g.204128709C= , CM000663.1:g.204128709C= GRCh37
NC_000001.9:g.202395332C= NCBI36
NG_012122.1:g.11757G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.507G= MANE Select ENSP00000272190.8:p.Thr169=
ENST00000638118.1:c.393G= ENSP00000490307.1:p.Thr131=
ENST00000272190.8:c.507G= ENSP00000272190.8:p.Thr169=
NM_000537.3:c.507G= NP_000528.1:p.Thr169=
NM_000537.4:c.507G= MANE Select NP_000528.1:p.Thr169=
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