Canonical Allele Identifier: CA339113958
Gene: SELENON HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.25809105C>A , CM000663.2:g.25809105C>A GRCh38
NC_000001.10:g.26135596C>A , CM000663.1:g.26135596C>A GRCh37
NC_000001.9:g.26008183C>A NCBI36
NG_009930.1:g.13930C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000354177.9:c.656C>A ENSP00000346109.5:p.Ala219Asp
ENST00000494537.2:c.725C>A ENSP00000508308.1:p.Ala242Asp
ENST00000361547.7:c.827C>A MANE Select ENSP00000355141.2:p.Ala276Asp
ENST00000354177.8:c.725C>A ENSP00000346109.4:p.Ala242Asp
ENST00000361547.6:c.827C>A ENSP00000355141.2:p.Ala276Asp
ENST00000374315.1:c.725C>A ENSP00000363434.1:p.Ala242Asp
NM_020451.2:c.827C>A NP_065184.2:p.Ala276Asp
NM_206926.1:c.725C>A NP_996809.1:p.Ala242Asp
NM_020451.3:c.827C>A MANE Select NP_065184.2:p.Ala276Asp
NM_206926.2:c.725C>A NP_996809.1:p.Ala242Asp