Canonical Allele Identifier: CA2482057570
Gene: REN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204160658C= , CM000663.2:g.204160658C= GRCh38
NC_000001.10:g.204129786C= , CM000663.1:g.204129786C= GRCh37
NC_000001.9:g.202396409C= NCBI36
NG_012122.1:g.10680G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.394G= MANE Select ENSP00000272190.8:p.Ala132=
ENST00000638118.1:c.280G= ENSP00000490307.1:p.Ala94=
ENST00000272190.8:c.394G= ENSP00000272190.8:p.Ala132=
NM_000537.3:c.394G= NP_000528.1:p.Ala132=
NM_000537.4:c.394G= MANE Select NP_000528.1:p.Ala132=