Canonical Allele Identifier: CA696839

Gene: SELENON

Linked Data

• dbSNP Id: rs775068018
• ExAC: 1:26139262 C / T
• gnomAD v2: 1-26139262-C-T
• gnomAD v4: 1-25812771-C-T
• MyVariant Identifiers: chr1:g.26139262C>T (hg19) ; chr1:g.25812771C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25812771C>T , CM000663.2:g.25812771C>T	GRCh38
NC_000001.10:g.26139262C>T , CM000663.1:g.26139262C>T	GRCh37
NC_000001.9:g.26011849C>T	NCBI36
NG_009930.1:g.17596C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354177.9:c.1195C>T	ENSP00000346109.5:p.Leu399=
ENST00000494537.2:c.1264C>T	ENSP00000508308.1:p.Leu422=
ENST00000361547.7:c.1366C>T MANE Select	ENSP00000355141.2:p.Leu456=
ENST00000354177.8:c.1264C>T	ENSP00000346109.4:p.Leu422=
ENST00000361547.6:c.1366C>T	ENSP00000355141.2:p.Leu456=
ENST00000374315.1:c.1264C>T	ENSP00000363434.1:p.Leu422=
ENST00000494537.1:n.44C>T
ENST00000559265.1:n.255+892C>T
ENST00000630065.2:c.-207C>T	ENSP00000487549.1:n.-207C>T
NM_020451.2:c.1366C>T	NP_065184.2:p.Leu456=
NM_206926.1:c.1264C>T	NP_996809.1:p.Leu422=
NM_020451.3:c.1366C>T MANE Select	NP_065184.2:p.Leu456=
NM_206926.2:c.1264C>T	NP_996809.1:p.Leu422=