Canonical Allele Identifier: CA344338711

Gene: REN

Linked Data

• MyVariant Identifiers: chr1:g.204128704G>T (hg19) ; chr1:g.204159576G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.204159576G>T , CM000663.2:g.204159576G>T	GRCh38
NC_000001.10:g.204128704G>T , CM000663.1:g.204128704G>T	GRCh37
NC_000001.9:g.202395327G>T	NCBI36
NG_012122.1:g.11762C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272190.9:c.512C>A MANE Select	ENSP00000272190.8:p.Thr171Lys
ENST00000638118.1:c.398C>A	ENSP00000490307.1:p.Thr133Lys
ENST00000272190.8:c.512C>A	ENSP00000272190.8:p.Thr171Lys
NM_000537.3:c.512C>A	NP_000528.1:p.Thr171Lys
NM_000537.4:c.512C>A MANE Select	NP_000528.1:p.Thr171Lys