Canonical Allele Identifier: CA2482057003
Gene: REN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159276G= , CM000663.2:g.204159276G= GRCh38
NC_000001.10:g.204128404G= , CM000663.1:g.204128404G= GRCh37
NC_000001.9:g.202395027G= NCBI36
NG_012122.1:g.12062C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.689+123C= MANE Select ENSP00000272190.8:n.689+123C=
ENST00000638118.1:c.575+123C= ENSP00000490307.1:n.575+123C=
ENST00000272190.8:c.689+123C= ENSP00000272190.8:n.689+123C=
NM_000537.3:c.689+123C= NP_000528.1:n.689+123C=
NM_000537.4:c.689+123C= MANE Select NP_000528.1:n.689+123C=