Canonical Allele Identifier: CA422833046
Gene: REN HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.204124150G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204155022G>A , CM000663.2:g.204155022G>A GRCh38
NC_000001.10:g.204124150G>A , CM000663.1:g.204124150G>A GRCh37
NC_000001.9:g.202390773G>A NCBI36
NG_012122.1:g.16316C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.1215C>T MANE Select ENSP00000272190.8:p.Ala405=
ENST00000638118.1:c.1101C>T ENSP00000490307.1:p.Ala367=
ENST00000272190.8:c.1215C>T ENSP00000272190.8:p.Ala405=
NM_000537.3:c.1215C>T NP_000528.1:p.Ala405=
NM_000537.4:c.1215C>T MANE Select NP_000528.1:p.Ala405=