Canonical Allele Identifier: CA344338759

Gene: REN

Linked Data

• MyVariant Identifiers: chr1:g.204128711T>G (hg19) ; chr1:g.204159583T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.204159583T>G , CM000663.2:g.204159583T>G	GRCh38
NC_000001.10:g.204128711T>G , CM000663.1:g.204128711T>G	GRCh37
NC_000001.9:g.202395334T>G	NCBI36
NG_012122.1:g.11755A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272190.9:c.505A>C MANE Select	ENSP00000272190.8:p.Thr169Pro
ENST00000638118.1:c.391A>C	ENSP00000490307.1:p.Thr131Pro
ENST00000272190.8:c.505A>C	ENSP00000272190.8:p.Thr169Pro
NM_000537.3:c.505A>C	NP_000528.1:p.Thr169Pro
NM_000537.4:c.505A>C MANE Select	NP_000528.1:p.Thr169Pro