Canonical Allele Identifier: CA1143991745
Gene: REN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204155203C= , CM000663.2:g.204155203C= GRCh38
NC_000001.10:g.204124331C= , CM000663.1:g.204124331C= GRCh37
NC_000001.9:g.202390954C= NCBI36
NG_012122.1:g.16135G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.1060-26G= MANE Select ENSP00000272190.8:n.1060-26G=
ENST00000638118.1:c.946-26G= ENSP00000490307.1:n.946-26G=
ENST00000272190.8:c.1060-26G= ENSP00000272190.8:n.1060-26G=
NM_000537.3:c.1060-26G= NP_000528.1:n.1060-26G=
NM_000537.4:c.1060-26G= MANE Select NP_000528.1:n.1060-26G=