Canonical Allele Identifier: CA422837337

Gene: REN

Linked Data

• MyVariant Identifiers: chr1:g.204128562C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.204159434C>T , CM000663.2:g.204159434C>T	GRCh38
NC_000001.10:g.204128562C>T , CM000663.1:g.204128562C>T	GRCh37
NC_000001.9:g.202395185C>T	NCBI36
NG_012122.1:g.11904G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272190.9:c.654G>A MANE Select	ENSP00000272190.8:p.Val218=
ENST00000638118.1:c.540G>A	ENSP00000490307.1:p.Val180=
ENST00000272190.8:c.654G>A	ENSP00000272190.8:p.Val218=
NM_000537.3:c.654G>A	NP_000528.1:p.Val218=
NM_000537.4:c.654G>A MANE Select	NP_000528.1:p.Val218=