Canonical Allele Identifier: CA1140492303
Gene: REN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159311T= , CM000663.2:g.204159311T= GRCh38
NC_000001.10:g.204128439T= , CM000663.1:g.204128439T= GRCh37
NC_000001.9:g.202395062T= NCBI36
NG_012122.1:g.12027A=

Transcript Alleles

HGVS Amino-acid change
ENST00000272190.9:c.689+88A= MANE Select ENSP00000272190.8:n.689+88A=
ENST00000638118.1:c.575+88A= ENSP00000490307.1:n.575+88A=
ENST00000272190.8:c.689+88A= ENSP00000272190.8:n.689+88A=
NM_000537.3:c.689+88A= NP_000528.1:n.689+88A=
NM_000537.4:c.689+88A= MANE Select NP_000528.1:n.689+88A=
Search 100 bp 5'
Search 100 bp 3'