Canonical Allele Identifier: CA1149118992
Gene: REN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159322C= , CM000663.2:g.204159322C= GRCh38
NC_000001.10:g.204128450C= , CM000663.1:g.204128450C= GRCh37
NC_000001.9:g.202395073C= NCBI36
NG_012122.1:g.12016G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.689+77G= MANE Select ENSP00000272190.8:n.689+77G=
ENST00000638118.1:c.575+77G= ENSP00000490307.1:n.575+77G=
ENST00000272190.8:c.689+77G= ENSP00000272190.8:n.689+77G=
NM_000537.3:c.689+77G= NP_000528.1:n.689+77G=
NM_000537.4:c.689+77G= MANE Select NP_000528.1:n.689+77G=