Canonical Allele Identifier: CA2573986889
Gene: REN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204155209C>A , CM000663.2:g.204155209C>A GRCh38
NC_000001.10:g.204124337C>A , CM000663.1:g.204124337C>A GRCh37
NC_000001.9:g.202390960C>A NCBI36
NG_012122.1:g.16129G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.1060-32G>T MANE Select ENSP00000272190.8:n.1060-32G>T
ENST00000638118.1:c.946-32G>T ENSP00000490307.1:n.946-32G>T
ENST00000272190.8:c.1060-32G>T ENSP00000272190.8:n.1060-32G>T
NM_000537.3:c.1060-32G>T NP_000528.1:n.1060-32G>T
NM_000537.4:c.1060-32G>T MANE Select NP_000528.1:n.1060-32G>T