Canonical Allele Identifier: CA422833235
Gene: REN HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.204124255A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204155127A>G , CM000663.2:g.204155127A>G GRCh38
NC_000001.10:g.204124255A>G , CM000663.1:g.204124255A>G GRCh37
NC_000001.9:g.202390878A>G NCBI36
NG_012122.1:g.16211T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.1110T>C MANE Select ENSP00000272190.8:p.Asp370=
ENST00000638118.1:c.996T>C ENSP00000490307.1:p.Asp332=
ENST00000272190.8:c.1110T>C ENSP00000272190.8:p.Asp370=
NM_000537.3:c.1110T>C NP_000528.1:p.Asp370=
NM_000537.4:c.1110T>C MANE Select NP_000528.1:p.Asp370=