Canonical Allele Identifier: CA2839804376
Gene: REN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204154998C>T , CM000663.2:g.204154998C>T GRCh38
NC_000001.10:g.204124126C>T , CM000663.1:g.204124126C>T GRCh37
NC_000001.9:g.202390749C>T NCBI36
NG_012122.1:g.16340G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.*18G>A MANE Select ENSP00000272190.8:n.*18G>A
ENST00000638118.1:c.*18G>A ENSP00000490307.1:n.*18G>A
ENST00000272190.8:c.*18G>A ENSP00000272190.8:n.*18G>A
NM_000537.3:c.*18G>A NP_000528.1:n.*18G>A
NM_000537.4:c.*18G>A MANE Select NP_000528.1:n.*18G>A
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