Canonical Allele Identifier: CA339117831

Gene: SELENON

Linked Data

• MyVariant Identifiers: chr1:g.26139257G>T (hg19) ; chr1:g.25812766G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25812766G>T , CM000663.2:g.25812766G>T	GRCh38
NC_000001.10:g.26139257G>T , CM000663.1:g.26139257G>T	GRCh37
NC_000001.9:g.26011844G>T	NCBI36
NG_009930.1:g.17591G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000354177.9:c.1190G>T	ENSP00000346109.5:p.Gly397Val
ENST00000494537.2:c.1259G>T	ENSP00000508308.1:p.Gly420Val
ENST00000361547.7:c.1361G>T MANE Select	ENSP00000355141.2:p.Gly454Val
ENST00000354177.8:c.1259G>T	ENSP00000346109.4:p.Gly420Val
ENST00000361547.6:c.1361G>T	ENSP00000355141.2:p.Gly454Val
ENST00000374315.1:c.1259G>T	ENSP00000363434.1:p.Gly420Val
ENST00000494537.1:n.39G>T
ENST00000559265.1:n.255+887G>T
ENST00000630065.2:c.-212G>T	ENSP00000487549.1:n.-212G>T
NM_020451.2:c.1361G>T	NP_065184.2:p.Gly454Val
NM_206926.1:c.1259G>T	NP_996809.1:p.Gly420Val
NM_020451.3:c.1361G>T MANE Select	NP_065184.2:p.Gly454Val
NM_206926.2:c.1259G>T	NP_996809.1:p.Gly420Val