Canonical Allele Identifier: CA19698938

Gene: SELENON

Linked Data

• dbSNP Id: rs374687219
• gnomAD v3: 1-25812768-G-A
• gnomAD v4: 1-25812768-G-A
• MyVariant Identifiers: chr1:g.26139259G>A (hg19) ; chr1:g.25812768G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25812768G>A , CM000663.2:g.25812768G>A	GRCh38
NC_000001.10:g.26139259G>A , CM000663.1:g.26139259G>A	GRCh37
NC_000001.9:g.26011846G>A	NCBI36
NG_009930.1:g.17593G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354177.9:c.1192G>A	ENSP00000346109.5:p.Ala398Thr
ENST00000494537.2:c.1261G>A	ENSP00000508308.1:p.Ala421Thr
ENST00000361547.7:c.1363G>A MANE Select	ENSP00000355141.2:p.Ala455Thr
ENST00000354177.8:c.1261G>A	ENSP00000346109.4:p.Ala421Thr
ENST00000361547.6:c.1363G>A	ENSP00000355141.2:p.Ala455Thr
ENST00000374315.1:c.1261G>A	ENSP00000363434.1:p.Ala421Thr
ENST00000494537.1:n.41G>A
ENST00000559265.1:n.255+889G>A
ENST00000630065.2:c.-210G>A	ENSP00000487549.1:n.-210G>A
NM_020451.2:c.1363G>A	NP_065184.2:p.Ala455Thr
NM_206926.1:c.1261G>A	NP_996809.1:p.Ala421Thr
NM_020451.3:c.1363G>A MANE Select	NP_065184.2:p.Ala455Thr
NM_206926.2:c.1261G>A	NP_996809.1:p.Ala421Thr