Canonical Allele Identifier: CA344338534
Gene: REN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159549A>C , CM000663.2:g.204159549A>C GRCh38
NC_000001.10:g.204128677A>C , CM000663.1:g.204128677A>C GRCh37
NC_000001.9:g.202395300A>C NCBI36
NG_012122.1:g.11789T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.539T>G MANE Select ENSP00000272190.8:p.Met180Arg
ENST00000638118.1:c.425T>G ENSP00000490307.1:p.Met142Arg
ENST00000272190.8:c.539T>G ENSP00000272190.8:p.Met180Arg
NM_000537.3:c.539T>G NP_000528.1:p.Met180Arg
NM_000537.4:c.539T>G MANE Select NP_000528.1:p.Met180Arg