Canonical Allele Identifier: CA422833147
Gene: REN HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.204124207G>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204155079G>T , CM000663.2:g.204155079G>T GRCh38
NC_000001.10:g.204124207G>T , CM000663.1:g.204124207G>T GRCh37
NC_000001.9:g.202390830G>T NCBI36
NG_012122.1:g.16259C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000272190.9:c.1158C>A MANE Select ENSP00000272190.8:p.Ile386=
ENST00000638118.1:c.1044C>A ENSP00000490307.1:p.Ile348=
ENST00000272190.8:c.1158C>A ENSP00000272190.8:p.Ile386=
NM_000537.3:c.1158C>A NP_000528.1:p.Ile386=
NM_000537.4:c.1158C>A MANE Select NP_000528.1:p.Ile386=
Search 100 bp 5'
Search 100 bp 3'