Canonical Allele Identifier: CA2482055238
Gene: REN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204155090C= , CM000663.2:g.204155090C= GRCh38
NC_000001.10:g.204124218C= , CM000663.1:g.204124218C= GRCh37
NC_000001.9:g.202390841C= NCBI36
NG_012122.1:g.16248G=

Transcript Alleles

HGVS Amino-acid change
ENST00000272190.9:c.1147G= MANE Select ENSP00000272190.8:p.Ala383=
ENST00000638118.1:c.1033G= ENSP00000490307.1:p.Ala345=
ENST00000272190.8:c.1147G= ENSP00000272190.8:p.Ala383=
NM_000537.3:c.1147G= NP_000528.1:p.Ala383=
NM_000537.4:c.1147G= MANE Select NP_000528.1:p.Ala383=