Canonical Allele Identifier: CA416759233

Gene: SELENON

Linked Data

• MyVariant Identifiers: chr1:g.26139180C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25812689C>T , CM000663.2:g.25812689C>T	GRCh38
NC_000001.10:g.26139180C>T , CM000663.1:g.26139180C>T	GRCh37
NC_000001.9:g.26011767C>T	NCBI36
NG_009930.1:g.17514C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000354177.9:c.1113C>T	ENSP00000346109.5:p.Val371=
ENST00000494537.2:c.1182C>T	ENSP00000508308.1:p.Val394=
ENST00000361547.7:c.1284C>T MANE Select	ENSP00000355141.2:p.Val428=
ENST00000354177.8:c.1182C>T	ENSP00000346109.4:p.Val394=
ENST00000361547.6:c.1284C>T	ENSP00000355141.2:p.Val428=
ENST00000374315.1:c.1182C>T	ENSP00000363434.1:p.Val394=
ENST00000559265.1:n.255+810C>T
ENST00000630065.2:c.-289C>T	ENSP00000487549.1:n.-289C>T
NM_020451.2:c.1284C>T	NP_065184.2:p.Val428=
NM_206926.1:c.1182C>T	NP_996809.1:p.Val394=
NM_020451.3:c.1284C>T MANE Select	NP_065184.2:p.Val428=
NM_206926.2:c.1182C>T	NP_996809.1:p.Val394=