Canonical Allele Identifier: CA422837475

Gene: REN

Linked Data

• MyVariant Identifiers: chr1:g.204128709C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.204159581C>G , CM000663.2:g.204159581C>G	GRCh38
NC_000001.10:g.204128709C>G , CM000663.1:g.204128709C>G	GRCh37
NC_000001.9:g.202395332C>G	NCBI36
NG_012122.1:g.11757G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272190.9:c.507G>C MANE Select	ENSP00000272190.8:p.Thr169=
ENST00000638118.1:c.393G>C	ENSP00000490307.1:p.Thr131=
ENST00000272190.8:c.507G>C	ENSP00000272190.8:p.Thr169=
NM_000537.3:c.507G>C	NP_000528.1:p.Thr169=
NM_000537.4:c.507G>C MANE Select	NP_000528.1:p.Thr169=