Canonical Allele Identifier: CA253167

Gene: SELENON

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25812790G>A , CM000663.2:g.25812790G>A	GRCh38
NC_000001.10:g.26139281G>A , CM000663.1:g.26139281G>A	GRCh37
NC_000001.9:g.26011868G>A	NCBI36
NG_009930.1:g.17615G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354177.9:c.1214G>A	ENSP00000346109.5:p.Ter405=
ENST00000494537.2:c.1283G>A	ENSP00000508308.1:p.Ter428=
ENST00000361547.7:c.1385G>A MANE Select	ENSP00000355141.2:p.Ter462=
ENST00000354177.8:c.1274+9G>A	ENSP00000346109.4:n.1274+9G>A
ENST00000361547.6:c.1385G>A	ENSP00000355141.2:p.Ter462=
ENST00000374315.1:c.1283G>A	ENSP00000363434.1:p.Ter428=
ENST00000494537.1:n.63G>A
ENST00000559265.1:n.255+911G>A
ENST00000630065.2:c.-188G>A	ENSP00000487549.1:n.-188G>A
NM_020451.2:c.1385G>A	NP_065184.2:p.Ter462=
NM_206926.1:c.1283G>A	NP_996809.1:p.Ter428=
NM_020451.3:c.1385G>A MANE Select	NP_065184.2:p.Ter462=
NM_206926.2:c.1283G>A	NP_996809.1:p.Ter428=