Canonical Allele Identifier: CA339113965
Gene: SELENON HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.25809107T>A , CM000663.2:g.25809107T>A GRCh38
NC_000001.10:g.26135598T>A , CM000663.1:g.26135598T>A GRCh37
NC_000001.9:g.26008185T>A NCBI36
NG_009930.1:g.13932T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000354177.9:c.658T>A ENSP00000346109.5:p.Cys220Ser
ENST00000494537.2:c.727T>A ENSP00000508308.1:p.Cys243Ser
ENST00000361547.7:c.829T>A MANE Select ENSP00000355141.2:p.Cys277Ser
ENST00000354177.8:c.727T>A ENSP00000346109.4:p.Cys243Ser
ENST00000361547.6:c.829T>A ENSP00000355141.2:p.Cys277Ser
ENST00000374315.1:c.727T>A ENSP00000363434.1:p.Cys243Ser
NM_020451.2:c.829T>A NP_065184.2:p.Cys277Ser
NM_206926.1:c.727T>A NP_996809.1:p.Cys243Ser
NM_020451.3:c.829T>A MANE Select NP_065184.2:p.Cys277Ser
NM_206926.2:c.727T>A NP_996809.1:p.Cys243Ser