Canonical Allele Identifier: CA2482055222
Gene: REN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204155080A= , CM000663.2:g.204155080A= GRCh38
NC_000001.10:g.204124208A= , CM000663.1:g.204124208A= GRCh37
NC_000001.9:g.202390831A= NCBI36
NG_012122.1:g.16258T=

Transcript Alleles

HGVS Amino-acid change
ENST00000272190.9:c.1157T= MANE Select ENSP00000272190.8:p.Ile386=
ENST00000638118.1:c.1043T= ENSP00000490307.1:p.Ile348=
ENST00000272190.8:c.1157T= ENSP00000272190.8:p.Ile386=
NM_000537.3:c.1157T= NP_000528.1:p.Ile386=
NM_000537.4:c.1157T= MANE Select NP_000528.1:p.Ile386=