Canonical Allele Identifier: CA339119009

Gene: SELENON

Linked Data

• MyVariant Identifiers: chr1:g.26140393A>T (hg19) ; chr1:g.25813902A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25813902A>T , CM000663.2:g.25813902A>T	GRCh38
NC_000001.10:g.26140393A>T , CM000663.1:g.26140393A>T	GRCh37
NC_000001.9:g.26012980A>T	NCBI36
NG_009930.1:g.18727A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000354177.9:c.1238A>T	ENSP00000346109.5:p.Glu413Val
ENST00000494537.2:c.1396A>T	ENSP00000508308.1:p.Arg466Ter
ENST00000361547.7:c.1409A>T MANE Select	ENSP00000355141.2:p.Glu470Val
ENST00000354177.8:c.1307A>T	ENSP00000346109.4:p.Glu436Val
ENST00000361547.6:c.1409A>T	ENSP00000355141.2:p.Glu470Val
ENST00000374315.1:c.1307A>T	ENSP00000363434.1:p.Glu436Val
ENST00000494537.1:n.176A>T
ENST00000559265.1:n.255+2023A>T
ENST00000630065.2:c.-164A>T	ENSP00000487549.1:n.-164A>T
NM_020451.2:c.1409A>T	NP_065184.2:p.Glu470Val
NM_206926.1:c.1307A>T	NP_996809.1:p.Glu436Val
NM_020451.3:c.1409A>T MANE Select	NP_065184.2:p.Glu470Val
NM_206926.2:c.1307A>T	NP_996809.1:p.Glu436Val