Canonical Allele Identifier: CA2482057129
Gene: REN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159609_204159610delinsGA , CM000663.2:g.204159609_204159610delinsGA GRCh38
NC_000001.10:g.204128737_204128738delinsGA , CM000663.1:g.204128737_204128738delinsGA GRCh37
NC_000001.9:g.202395360_202395361delinsGA NCBI36
NG_012122.1:g.11728_11729delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.493-15_493-14delinsTC MANE Select ENSP00000272190.8:n.493-15_493-14delinsTC
ENST00000638118.1:c.379-15_379-14delinsTC ENSP00000490307.1:n.379-15_379-14delinsTC
ENST00000272190.8:c.493-15_493-14delinsTC ENSP00000272190.8:n.493-15_493-14delinsTC
NM_000537.3:c.493-15_493-14delinsTC NP_000528.1:n.493-15_493-14delinsTC
NM_000537.4:c.493-15_493-14delinsTC MANE Select NP_000528.1:n.493-15_493-14delinsTC