Canonical Allele Identifier: CA645513027

Gene: SELENON

Linked Data

• gnomAD v4: 1-25812762-TG-T
• COSMIC: COSM6033948 ; COSM6033949

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25812768del , CM000663.2:g.25812768del	GRCh38
NC_000001.10:g.26139259del , CM000663.1:g.26139259del	GRCh37
NC_000001.9:g.26011846del	NCBI36
NG_009930.1:g.17593del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354177.9:c.1192del	ENSP00000346109.5:p.Ala398ProfsTer?
ENST00000494537.2:c.1261del	ENSP00000508308.1:p.Ala421ProfsTer15
ENST00000361547.7:c.1363del MANE Select	ENSP00000355141.2:p.Ala455ProfsTer?
ENST00000354177.8:c.1261del	ENSP00000346109.4:p.Ala421ProfsTer?
ENST00000361547.6:c.1363del	ENSP00000355141.2:p.Ala455ProfsTer?
ENST00000374315.1:c.1261del	ENSP00000363434.1:p.Ala421ProfsTer?
ENST00000494537.1:n.41del
ENST00000559265.1:n.255+889del
ENST00000630065.2:c.-210del	ENSP00000487549.1:n.-210del
NM_020451.2:c.1363del	NP_065184.2:p.Ala455ProfsTer?
NM_206926.1:c.1261del	NP_996809.1:p.Ala421ProfsTer?
NM_020451.3:c.1363del MANE Select	NP_065184.2:p.Ala455ProfsTer?
NM_206926.2:c.1261del	NP_996809.1:p.Ala421ProfsTer?