Canonical Allele Identifier: CA2482059827
Gene: REN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204166258C= , CM000663.2:g.204166258C= GRCh38
NC_000001.10:g.204135386C= , CM000663.1:g.204135386C= GRCh37
NC_000001.9:g.202402009C= NCBI36
NG_012122.1:g.5080G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.36G= MANE Select ENSP00000272190.8:p.Leu12=
ENST00000638118.1:c.-16-4095G= ENSP00000490307.1:n.-16-4095G=
ENST00000272190.8:c.36G= ENSP00000272190.8:p.Leu12=
NM_000537.3:c.36G= NP_000528.1:p.Leu12=
NM_000537.4:c.36G= MANE Select NP_000528.1:p.Leu12=