Canonical Allele Identifier: CA422837457

Gene: REN

Linked Data

• MyVariant Identifiers: chr1:g.204128688C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.204159560C>T , CM000663.2:g.204159560C>T	GRCh38
NC_000001.10:g.204128688C>T , CM000663.1:g.204128688C>T	GRCh37
NC_000001.9:g.202395311C>T	NCBI36
NG_012122.1:g.11778G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272190.9:c.528G>A MANE Select	ENSP00000272190.8:p.Glu176=
ENST00000638118.1:c.414G>A	ENSP00000490307.1:p.Glu138=
ENST00000272190.8:c.528G>A	ENSP00000272190.8:p.Glu176=
NM_000537.3:c.528G>A	NP_000528.1:p.Glu176=
NM_000537.4:c.528G>A MANE Select	NP_000528.1:p.Glu176=