Canonical Allele Identifier: CA2482057035
Gene: REN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159361T= , CM000663.2:g.204159361T= GRCh38
NC_000001.10:g.204128489T= , CM000663.1:g.204128489T= GRCh37
NC_000001.9:g.202395112T= NCBI36
NG_012122.1:g.11977A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.689+38A= MANE Select ENSP00000272190.8:n.689+38A=
ENST00000638118.1:c.575+38A= ENSP00000490307.1:n.575+38A=
ENST00000272190.8:c.689+38A= ENSP00000272190.8:n.689+38A=
NM_000537.3:c.689+38A= NP_000528.1:n.689+38A=
NM_000537.4:c.689+38A= MANE Select NP_000528.1:n.689+38A=