Canonical Allele Identifier: CA344338595

Gene: REN

Linked Data

• MyVariant Identifiers: chr1:g.204128688C>A (hg19) ; chr1:g.204159560C>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272190.9:c.528G>T MANE Select	ENSP00000272190.8:p.Glu176Asp
ENST00000638118.1:c.414G>T	ENSP00000490307.1:p.Glu138Asp
ENST00000272190.8:c.528G>T	ENSP00000272190.8:p.Glu176Asp
NM_000537.3:c.528G>T	NP_000528.1:p.Glu176Asp
NM_000537.4:c.528G>T MANE Select	NP_000528.1:p.Glu176Asp