Canonical Allele Identifier: CA422840554
Gene: REN HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.204135380C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204166252C>A , CM000663.2:g.204166252C>A GRCh38
NC_000001.10:g.204135380C>A , CM000663.1:g.204135380C>A GRCh37
NC_000001.9:g.202402003C>A NCBI36
NG_012122.1:g.5086G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000272190.9:c.42G>T MANE Select ENSP00000272190.8:p.Leu14=
ENST00000638118.1:c.-16-4089G>T ENSP00000490307.1:n.-16-4089G>T
ENST00000272190.8:c.42G>T ENSP00000272190.8:p.Leu14=
NM_000537.3:c.42G>T NP_000528.1:p.Leu14=
NM_000537.4:c.42G>T MANE Select NP_000528.1:p.Leu14=