Canonical Allele Identifier: CA416759053

Gene: SELENON

Linked Data

• MyVariant Identifiers: chr1:g.26135540C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25809049C>T , CM000663.2:g.25809049C>T	GRCh38
NC_000001.10:g.26135540C>T , CM000663.1:g.26135540C>T	GRCh37
NC_000001.9:g.26008127C>T	NCBI36
NG_009930.1:g.13874C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354177.9:c.646-46C>T	ENSP00000346109.5:n.646-46C>T
ENST00000494537.2:c.669C>T	ENSP00000508308.1:p.Ser223=
ENST00000361547.7:c.771C>T MANE Select	ENSP00000355141.2:p.Ser257=
ENST00000354177.8:c.669C>T	ENSP00000346109.4:p.Ser223=
ENST00000361547.6:c.771C>T	ENSP00000355141.2:p.Ser257=
ENST00000374315.1:c.669C>T	ENSP00000363434.1:p.Ser223=
NM_020451.2:c.771C>T	NP_065184.2:p.Ser257=
NM_206926.1:c.669C>T	NP_996809.1:p.Ser223=
NM_020451.3:c.771C>T MANE Select	NP_065184.2:p.Ser257=
NM_206926.2:c.669C>T	NP_996809.1:p.Ser223=