Canonical Allele Identifier: CA344337732

Gene: REN

Linked Data

• MyVariant Identifiers: chr1:g.204128551T>G (hg19) ; chr1:g.204159423T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.204159423T>G , CM000663.2:g.204159423T>G	GRCh38
NC_000001.10:g.204128551T>G , CM000663.1:g.204128551T>G	GRCh37
NC_000001.9:g.202395174T>G	NCBI36
NG_012122.1:g.11915A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272190.9:c.665A>C MANE Select	ENSP00000272190.8:p.Asp222Ala
ENST00000638118.1:c.551A>C	ENSP00000490307.1:p.Asp184Ala
ENST00000272190.8:c.665A>C	ENSP00000272190.8:p.Asp222Ala
NM_000537.3:c.665A>C	NP_000528.1:p.Asp222Ala
NM_000537.4:c.665A>C MANE Select	NP_000528.1:p.Asp222Ala