Canonical Allele Identifier: CA2482057056
Gene: REN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204159395_204159397delinsCCA , CM000663.2:g.204159395_204159397delinsCCA GRCh38
NC_000001.10:g.204128523_204128525delinsCCA , CM000663.1:g.204128523_204128525delinsCCA GRCh37
NC_000001.9:g.202395146_202395148delinsCCA NCBI36
NG_012122.1:g.11941_11943delinsTGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.689+2_689+4delinsTGG MANE Select ENSP00000272190.8:n.689+2_689+4delinsTGG
ENST00000638118.1:c.575+2_575+4delinsTGG ENSP00000490307.1:n.575+2_575+4delinsTGG
ENST00000272190.8:c.689+2_689+4delinsTGG ENSP00000272190.8:n.689+2_689+4delinsTGG
NM_000537.3:c.689+2_689+4delinsTGG NP_000528.1:n.689+2_689+4delinsTGG
NM_000537.4:c.689+2_689+4delinsTGG MANE Select NP_000528.1:n.689+2_689+4delinsTGG