Canonical Allele Identifier: CA2739670922
Gene: REN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159346T>G , CM000663.2:g.204159346T>G GRCh38
NC_000001.10:g.204128474T>G , CM000663.1:g.204128474T>G GRCh37
NC_000001.9:g.202395097T>G NCBI36
NG_012122.1:g.11992A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.689+53A>C MANE Select ENSP00000272190.8:n.689+53A>C
ENST00000638118.1:c.575+53A>C ENSP00000490307.1:n.575+53A>C
ENST00000272190.8:c.689+53A>C ENSP00000272190.8:n.689+53A>C
NM_000537.3:c.689+53A>C NP_000528.1:n.689+53A>C
NM_000537.4:c.689+53A>C MANE Select NP_000528.1:n.689+53A>C