Canonical Allele Identifier: CA344332279

Gene: REN

Linked Data

• COSMIC: COSM4027218
• MyVariant Identifiers: chr1:g.204124212A>T (hg19) ; chr1:g.204155084A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.204155084A>T , CM000663.2:g.204155084A>T	GRCh38
NC_000001.10:g.204124212A>T , CM000663.1:g.204124212A>T	GRCh37
NC_000001.9:g.202390835A>T	NCBI36
NG_012122.1:g.16254T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000272190.9:c.1153T>A MANE Select	ENSP00000272190.8:p.Phe385Ile
ENST00000638118.1:c.1039T>A	ENSP00000490307.1:p.Phe347Ile
ENST00000272190.8:c.1153T>A	ENSP00000272190.8:p.Phe385Ile
NM_000537.3:c.1153T>A	NP_000528.1:p.Phe385Ile
NM_000537.4:c.1153T>A MANE Select	NP_000528.1:p.Phe385Ile