Canonical Allele Identifier: CA2650014091
Gene: REN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159270G>A , CM000663.2:g.204159270G>A GRCh38
NC_000001.10:g.204128398G>A , CM000663.1:g.204128398G>A GRCh37
NC_000001.9:g.202395021G>A NCBI36
NG_012122.1:g.12068C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.689+129C>T MANE Select ENSP00000272190.8:n.689+129C>T
ENST00000638118.1:c.575+129C>T ENSP00000490307.1:n.575+129C>T
ENST00000272190.8:c.689+129C>T ENSP00000272190.8:n.689+129C>T
NM_000537.3:c.689+129C>T NP_000528.1:n.689+129C>T
NM_000537.4:c.689+129C>T MANE Select NP_000528.1:n.689+129C>T