Canonical Allele Identifier: CA2482055224
Gene: REN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204155081T= , CM000663.2:g.204155081T= GRCh38
NC_000001.10:g.204124209T= , CM000663.1:g.204124209T= GRCh37
NC_000001.9:g.202390832T= NCBI36
NG_012122.1:g.16257A=

Transcript Alleles

HGVS Amino-acid change
ENST00000272190.9:c.1156A= MANE Select ENSP00000272190.8:p.Ile386=
ENST00000638118.1:c.1042A= ENSP00000490307.1:p.Ile348=
ENST00000272190.8:c.1156A= ENSP00000272190.8:p.Ile386=
NM_000537.3:c.1156A= NP_000528.1:p.Ile386=
NM_000537.4:c.1156A= MANE Select NP_000528.1:p.Ile386=