Canonical Allele Identifier: CA2482057092
Gene: REN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159504C= , CM000663.2:g.204159504C= GRCh38
NC_000001.10:g.204128632C= , CM000663.1:g.204128632C= GRCh37
NC_000001.9:g.202395255C= NCBI36
NG_012122.1:g.11834G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.584G= MANE Select ENSP00000272190.8:p.Gly195=
ENST00000638118.1:c.470G= ENSP00000490307.1:p.Gly157=
ENST00000272190.8:c.584G= ENSP00000272190.8:p.Gly195=
NM_000537.3:c.584G= NP_000528.1:p.Gly195=
NM_000537.4:c.584G= MANE Select NP_000528.1:p.Gly195=