Canonical Allele Identifier: CA2740216847
Gene: REN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159604G>T , CM000663.2:g.204159604G>T GRCh38
NC_000001.10:g.204128732G>T , CM000663.1:g.204128732G>T GRCh37
NC_000001.9:g.202395355G>T NCBI36
NG_012122.1:g.11734C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.493-9C>A MANE Select ENSP00000272190.8:n.493-9C>A
ENST00000638118.1:c.379-9C>A ENSP00000490307.1:n.379-9C>A
ENST00000272190.8:c.493-9C>A ENSP00000272190.8:n.493-9C>A
NM_000537.3:c.493-9C>A NP_000528.1:n.493-9C>A
NM_000537.4:c.493-9C>A MANE Select NP_000528.1:n.493-9C>A
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