Canonical Allele Identifier: CA416759088

Gene: SELENON

Linked Data

• MyVariant Identifiers: chr1:g.26135591T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25809100T>G , CM000663.2:g.25809100T>G	GRCh38
NC_000001.10:g.26135591T>G , CM000663.1:g.26135591T>G	GRCh37
NC_000001.9:g.26008178T>G	NCBI36
NG_009930.1:g.13925T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000354177.9:c.651T>G	ENSP00000346109.5:p.Ala217=
ENST00000494537.2:c.720T>G	ENSP00000508308.1:p.Ala240=
ENST00000361547.7:c.822T>G MANE Select	ENSP00000355141.2:p.Ala274=
ENST00000354177.8:c.720T>G	ENSP00000346109.4:p.Ala240=
ENST00000361547.6:c.822T>G	ENSP00000355141.2:p.Ala274=
ENST00000374315.1:c.720T>G	ENSP00000363434.1:p.Ala240=
NM_020451.2:c.822T>G	NP_065184.2:p.Ala274=
NM_206926.1:c.720T>G	NP_996809.1:p.Ala240=
NM_020451.3:c.822T>G MANE Select	NP_065184.2:p.Ala274=
NM_206926.2:c.720T>G	NP_996809.1:p.Ala240=