Canonical Allele Identifier: CA339113590

Gene: SELENON

Linked Data

• MyVariant Identifiers: chr1:g.26135551C>A (hg19) ; chr1:g.25809060C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25809060C>A , CM000663.2:g.25809060C>A	GRCh38
NC_000001.10:g.26135551C>A , CM000663.1:g.26135551C>A	GRCh37
NC_000001.9:g.26008138C>A	NCBI36
NG_009930.1:g.13885C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354177.9:c.646-35C>A	ENSP00000346109.5:n.646-35C>A
ENST00000494537.2:c.680C>A	ENSP00000508308.1:p.Pro227His
ENST00000361547.7:c.782C>A MANE Select	ENSP00000355141.2:p.Pro261His
ENST00000354177.8:c.680C>A	ENSP00000346109.4:p.Pro227His
ENST00000361547.6:c.782C>A	ENSP00000355141.2:p.Pro261His
ENST00000374315.1:c.680C>A	ENSP00000363434.1:p.Pro227His
NM_020451.2:c.782C>A	NP_065184.2:p.Pro261His
NM_206926.1:c.680C>A	NP_996809.1:p.Pro227His
NM_020451.3:c.782C>A MANE Select	NP_065184.2:p.Pro261His
NM_206926.2:c.680C>A	NP_996809.1:p.Pro227His