Canonical Allele Identifier: CA344338293
Gene: REN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159519A>G , CM000663.2:g.204159519A>G GRCh38
NC_000001.10:g.204128647A>G , CM000663.1:g.204128647A>G GRCh37
NC_000001.9:g.202395270A>G NCBI36
NG_012122.1:g.11819T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.569T>C MANE Select ENSP00000272190.8:p.Phe190Ser
ENST00000638118.1:c.455T>C ENSP00000490307.1:p.Phe152Ser
ENST00000272190.8:c.569T>C ENSP00000272190.8:p.Phe190Ser
NM_000537.3:c.569T>C NP_000528.1:p.Phe190Ser
NM_000537.4:c.569T>C MANE Select NP_000528.1:p.Phe190Ser