Canonical Allele Identifier: CA339113960

Gene: SELENON

Linked Data

• gnomAD v4: 1-25809105-C-G
• MyVariant Identifiers: chr1:g.26135596C>G (hg19) ; chr1:g.25809105C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25809105C>G , CM000663.2:g.25809105C>G	GRCh38
NC_000001.10:g.26135596C>G , CM000663.1:g.26135596C>G	GRCh37
NC_000001.9:g.26008183C>G	NCBI36
NG_009930.1:g.13930C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000354177.9:c.656C>G	ENSP00000346109.5:p.Ala219Gly
ENST00000494537.2:c.725C>G	ENSP00000508308.1:p.Ala242Gly
ENST00000361547.7:c.827C>G MANE Select	ENSP00000355141.2:p.Ala276Gly
ENST00000354177.8:c.725C>G	ENSP00000346109.4:p.Ala242Gly
ENST00000361547.6:c.827C>G	ENSP00000355141.2:p.Ala276Gly
ENST00000374315.1:c.725C>G	ENSP00000363434.1:p.Ala242Gly
NM_020451.2:c.827C>G	NP_065184.2:p.Ala276Gly
NM_206926.1:c.725C>G	NP_996809.1:p.Ala242Gly
NM_020451.3:c.827C>G MANE Select	NP_065184.2:p.Ala276Gly
NM_206926.2:c.725C>G	NP_996809.1:p.Ala242Gly