Canonical Allele Identifier: CA339113947

Gene: SELENON

Linked Data

• MyVariant Identifiers: chr1:g.26135595G>A (hg19) ; chr1:g.25809104G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25809104G>A , CM000663.2:g.25809104G>A	GRCh38
NC_000001.10:g.26135595G>A , CM000663.1:g.26135595G>A	GRCh37
NC_000001.9:g.26008182G>A	NCBI36
NG_009930.1:g.13929G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000354177.9:c.655G>A	ENSP00000346109.5:p.Ala219Thr
ENST00000494537.2:c.724G>A	ENSP00000508308.1:p.Ala242Thr
ENST00000361547.7:c.826G>A MANE Select	ENSP00000355141.2:p.Ala276Thr
ENST00000354177.8:c.724G>A	ENSP00000346109.4:p.Ala242Thr
ENST00000361547.6:c.826G>A	ENSP00000355141.2:p.Ala276Thr
ENST00000374315.1:c.724G>A	ENSP00000363434.1:p.Ala242Thr
NM_020451.2:c.826G>A	NP_065184.2:p.Ala276Thr
NM_206926.1:c.724G>A	NP_996809.1:p.Ala242Thr
NM_020451.3:c.826G>A MANE Select	NP_065184.2:p.Ala276Thr
NM_206926.2:c.724G>A	NP_996809.1:p.Ala242Thr