Canonical Allele Identifier: CA344332468

Gene: REN

Linked Data

• MyVariant Identifiers: chr1:g.204124289T>G (hg19) ; chr1:g.204155161T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.204155161T>G , CM000663.2:g.204155161T>G	GRCh38
NC_000001.10:g.204124289T>G , CM000663.1:g.204124289T>G	GRCh37
NC_000001.9:g.202390912T>G	NCBI36
NG_012122.1:g.16177A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272190.9:c.1076A>C MANE Select	ENSP00000272190.8:p.Lys359Thr
ENST00000638118.1:c.962A>C	ENSP00000490307.1:p.Lys321Thr
ENST00000272190.8:c.1076A>C	ENSP00000272190.8:p.Lys359Thr
NM_000537.3:c.1076A>C	NP_000528.1:p.Lys359Thr
NM_000537.4:c.1076A>C MANE Select	NP_000528.1:p.Lys359Thr