Canonical Allele Identifier: CA2742889995

Gene: SELENON

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25812767_25812768dup , CM000663.2:g.25812767_25812768dup	GRCh38
NC_000001.10:g.26139258_26139259dup , CM000663.1:g.26139258_26139259dup	GRCh37
NC_000001.9:g.26011845_26011846dup	NCBI36
NG_009930.1:g.17592_17593dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354177.9:c.1191_1192dup	ENSP00000346109.5:p.Ala398GlyfsTer?
ENST00000494537.2:c.1260_1261dup	ENSP00000508308.1:p.Ala421GlyfsTer16
ENST00000361547.7:c.1362_1363dup MANE Select	ENSP00000355141.2:p.Ala455GlyfsTer?
ENST00000354177.8:c.1260_1261dup	ENSP00000346109.4:p.Ala421GlyfsTer?
ENST00000361547.6:c.1362_1363dup	ENSP00000355141.2:p.Ala455GlyfsTer?
ENST00000374315.1:c.1260_1261dup	ENSP00000363434.1:p.Ala421GlyfsTer?
ENST00000494537.1:n.40_41dup
ENST00000559265.1:n.255+888_255+889dup
ENST00000630065.2:c.-211_-210dup	ENSP00000487549.1:n.-211_-210dup
NM_020451.2:c.1362_1363dup	NP_065184.2:p.Ala455GlyfsTer?
NM_206926.1:c.1260_1261dup	NP_996809.1:p.Ala421GlyfsTer?
NM_020451.3:c.1362_1363dup MANE Select	NP_065184.2:p.Ala455GlyfsTer?
NM_206926.2:c.1260_1261dup	NP_996809.1:p.Ala421GlyfsTer?