Canonical Allele Identifier: CA344338826

Gene: REN

Linked Data

• MyVariant Identifiers: chr1:g.204128722A>G (hg19) ; chr1:g.204159594A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.204159594A>G , CM000663.2:g.204159594A>G	GRCh38
NC_000001.10:g.204128722A>G , CM000663.1:g.204128722A>G	GRCh37
NC_000001.9:g.202395345A>G	NCBI36
NG_012122.1:g.11744T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272190.9:c.494T>C MANE Select	ENSP00000272190.8:p.Val165Ala
ENST00000638118.1:c.380T>C	ENSP00000490307.1:p.Val127Ala
ENST00000272190.8:c.494T>C	ENSP00000272190.8:p.Val165Ala
NM_000537.3:c.494T>C	NP_000528.1:p.Val165Ala
NM_000537.4:c.494T>C MANE Select	NP_000528.1:p.Val165Ala