Canonical Allele Identifier: CA422837469

Gene: REN

Linked Data

• MyVariant Identifiers: chr1:g.204128706C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.204159578C>T , CM000663.2:g.204159578C>T	GRCh38
NC_000001.10:g.204128706C>T , CM000663.1:g.204128706C>T	GRCh37
NC_000001.9:g.202395329C>T	NCBI36
NG_012122.1:g.11760G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272190.9:c.510G>A MANE Select	ENSP00000272190.8:p.Val170=
ENST00000638118.1:c.396G>A	ENSP00000490307.1:p.Val132=
ENST00000272190.8:c.510G>A	ENSP00000272190.8:p.Val170=
NM_000537.3:c.510G>A	NP_000528.1:p.Val170=
NM_000537.4:c.510G>A MANE Select	NP_000528.1:p.Val170=