Canonical Allele Identifier: CA734440911

Gene: SELENON

Linked Data

• dbSNP Id: rs1420418572
• gnomAD v3: 1-25809275-G-A
• gnomAD v4: 1-25809275-G-A
• MyVariant Identifiers: chr1:g.26135766G>A (hg19) ; chr1:g.25809275G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25809275G>A , CM000663.2:g.25809275G>A	GRCh38
NC_000001.10:g.26135766G>A , CM000663.1:g.26135766G>A	GRCh37
NC_000001.9:g.26008353G>A	NCBI36
NG_009930.1:g.14100G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354177.9:c.701+125G>A	ENSP00000346109.5:n.701+125G>A
ENST00000494537.2:c.770+125G>A	ENSP00000508308.1:n.770+125G>A
ENST00000361547.7:c.872+125G>A MANE Select	ENSP00000355141.2:n.872+125G>A
ENST00000354177.8:c.770+125G>A	ENSP00000346109.4:n.770+125G>A
ENST00000361547.6:c.872+125G>A	ENSP00000355141.2:n.872+125G>A
ENST00000374315.1:c.770+125G>A	ENSP00000363434.1:n.770+125G>A
NM_020451.2:c.872+125G>A	NP_065184.2:n.872+125G>A
NM_206926.1:c.770+125G>A	NP_996809.1:n.770+125G>A
NM_020451.3:c.872+125G>A MANE Select	NP_065184.2:n.872+125G>A
NM_206926.2:c.770+125G>A	NP_996809.1:n.770+125G>A