Canonical Allele Identifier: CA344337920
Gene: REN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159452G>T , CM000663.2:g.204159452G>T GRCh38
NC_000001.10:g.204128580G>T , CM000663.1:g.204128580G>T GRCh37
NC_000001.9:g.202395203G>T NCBI36
NG_012122.1:g.11886C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.636C>A MANE Select ENSP00000272190.8:p.Asn212Lys
ENST00000638118.1:c.522C>A ENSP00000490307.1:p.Asn174Lys
ENST00000272190.8:c.636C>A ENSP00000272190.8:p.Asn212Lys
NM_000537.3:c.636C>A NP_000528.1:p.Asn212Lys
NM_000537.4:c.636C>A MANE Select NP_000528.1:p.Asn212Lys