Canonical Allele Identifier: CA422833308
Gene: REN HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.204124291A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204155163A>G , CM000663.2:g.204155163A>G GRCh38
NC_000001.10:g.204124291A>G , CM000663.1:g.204124291A>G GRCh37
NC_000001.9:g.202390914A>G NCBI36
NG_012122.1:g.16175T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.1074T>C MANE Select ENSP00000272190.8:p.Ser358=
ENST00000638118.1:c.960T>C ENSP00000490307.1:p.Ser320=
ENST00000272190.8:c.1074T>C ENSP00000272190.8:p.Ser358=
NM_000537.3:c.1074T>C NP_000528.1:p.Ser358=
NM_000537.4:c.1074T>C MANE Select NP_000528.1:p.Ser358=