Canonical Allele Identifier: CA2482055123
Gene: REN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204154979G= , CM000663.2:g.204154979G= GRCh38
NC_000001.10:g.204124107G= , CM000663.1:g.204124107G= GRCh37
NC_000001.9:g.202390730G= NCBI36
NG_012122.1:g.16359C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.*37C= MANE Select ENSP00000272190.8:n.*37C=
ENST00000638118.1:c.*37C= ENSP00000490307.1:n.*37C=
ENST00000272190.8:c.*37C= ENSP00000272190.8:n.*37C=
NM_000537.3:c.*37C= NP_000528.1:n.*37C=
NM_000537.4:c.*37C= MANE Select NP_000528.1:n.*37C=