Canonical Allele Identifier: CA2482059443
Gene: REN HGNC NCBI

Linked Data

dbSNP Id: rs1658324728

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204165319_204165321dup , CM000663.2:g.204165319_204165321dup GRCh38
NC_000001.10:g.204134447_204134449dup , CM000663.1:g.204134447_204134449dup GRCh37
NC_000001.9:g.202401070_202401072dup NCBI36
NG_012122.1:g.6019_6021dup

Transcript Alleles

HGVS Amino-acid change
ENST00000272190.9:c.98+877_98+879dup MANE Select ENSP00000272190.8:n.98+877_98+879dup
ENST00000638118.1:c.-16-3156_-16-3154dup ENSP00000490307.1:n.-16-3156_-16-3154dup
ENST00000272190.8:c.98+877_98+879dup ENSP00000272190.8:n.98+877_98+879dup
NM_000537.3:c.98+877_98+879dup NP_000528.1:n.98+877_98+879dup
NM_000537.4:c.98+877_98+879dup MANE Select NP_000528.1:n.98+877_98+879dup