Canonical Allele Identifier: CA2482055306
Gene: REN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204155215A= , CM000663.2:g.204155215A= GRCh38
NC_000001.10:g.204124343A= , CM000663.1:g.204124343A= GRCh37
NC_000001.9:g.202390966A= NCBI36
NG_012122.1:g.16123T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.1060-38T= MANE Select ENSP00000272190.8:n.1060-38T=
ENST00000638118.1:c.946-38T= ENSP00000490307.1:n.946-38T=
ENST00000272190.8:c.1060-38T= ENSP00000272190.8:n.1060-38T=
NM_000537.3:c.1060-38T= NP_000528.1:n.1060-38T=
NM_000537.4:c.1060-38T= MANE Select NP_000528.1:n.1060-38T=