Canonical Allele Identifier: CA344332276
Gene: REN HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.204124211A>T (hg19) chr1:g.204155083A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204155083A>T , CM000663.2:g.204155083A>T GRCh38
NC_000001.10:g.204124211A>T , CM000663.1:g.204124211A>T GRCh37
NC_000001.9:g.202390834A>T NCBI36
NG_012122.1:g.16255T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000272190.9:c.1154T>A MANE Select ENSP00000272190.8:p.Phe385Tyr
ENST00000638118.1:c.1040T>A ENSP00000490307.1:p.Phe347Tyr
ENST00000272190.8:c.1154T>A ENSP00000272190.8:p.Phe385Tyr
NM_000537.3:c.1154T>A NP_000528.1:p.Phe385Tyr
NM_000537.4:c.1154T>A MANE Select NP_000528.1:p.Phe385Tyr
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