Canonical Allele Identifier: CA2650012769
Gene: REN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204162217T>A , CM000663.2:g.204162217T>A GRCh38
NC_000001.10:g.204131345T>A , CM000663.1:g.204131345T>A GRCh37
NC_000001.9:g.202397968T>A NCBI36
NG_012122.1:g.9121A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.99-54A>T MANE Select ENSP00000272190.8:n.99-54A>T
ENST00000638118.1:c.-16-54A>T ENSP00000490307.1:n.-16-54A>T
ENST00000272190.8:c.99-54A>T ENSP00000272190.8:n.99-54A>T
NM_000537.3:c.99-54A>T NP_000528.1:n.99-54A>T
NM_000537.4:c.99-54A>T MANE Select NP_000528.1:n.99-54A>T