Canonical Allele Identifier: CA339117837

Gene: SELENON

Linked Data

• dbSNP Id: rs1356970085
• gnomAD v2: 1-26139260-C-T
• gnomAD v4: 1-25812769-C-T
• MyVariant Identifiers: chr1:g.26139260C>T (hg19) ; chr1:g.25812769C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25812769C>T , CM000663.2:g.25812769C>T	GRCh38
NC_000001.10:g.26139260C>T , CM000663.1:g.26139260C>T	GRCh37
NC_000001.9:g.26011847C>T	NCBI36
NG_009930.1:g.17594C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354177.9:c.1193C>T	ENSP00000346109.5:p.Ala398Val
ENST00000494537.2:c.1262C>T	ENSP00000508308.1:p.Ala421Val
ENST00000361547.7:c.1364C>T MANE Select	ENSP00000355141.2:p.Ala455Val
ENST00000354177.8:c.1262C>T	ENSP00000346109.4:p.Ala421Val
ENST00000361547.6:c.1364C>T	ENSP00000355141.2:p.Ala455Val
ENST00000374315.1:c.1262C>T	ENSP00000363434.1:p.Ala421Val
ENST00000494537.1:n.42C>T
ENST00000559265.1:n.255+890C>T
ENST00000630065.2:c.-209C>T	ENSP00000487549.1:n.-209C>T
NM_020451.2:c.1364C>T	NP_065184.2:p.Ala455Val
NM_206926.1:c.1262C>T	NP_996809.1:p.Ala421Val
NM_020451.3:c.1364C>T MANE Select	NP_065184.2:p.Ala455Val
NM_206926.2:c.1262C>T	NP_996809.1:p.Ala421Val