Canonical Allele Identifier: CA344342005
Gene: REN HGNC NCBI

Linked Data

COSMIC: COSM3710516
MyVariant Identifiers: chr1:g.204131248C>T (hg19) chr1:g.204162120C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204162120C>T , CM000663.2:g.204162120C>T GRCh38
NC_000001.10:g.204131248C>T , CM000663.1:g.204131248C>T GRCh37
NC_000001.9:g.202397871C>T NCBI36
NG_012122.1:g.9218G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000272190.9:c.142G>A MANE Select ENSP00000272190.8:p.Glu48Lys
ENST00000638118.1:c.28G>A ENSP00000490307.1:p.Glu10Lys
ENST00000272190.8:c.142G>A ENSP00000272190.8:p.Glu48Lys
NM_000537.3:c.142G>A NP_000528.1:p.Glu48Lys
NM_000537.4:c.142G>A MANE Select NP_000528.1:p.Glu48Lys
Search 100 bp 5'
Search 100 bp 3'