Canonical Allele Identifier: CA416759085

Gene: SELENON

Linked Data

• MyVariant Identifiers: chr1:g.26135588A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25809097A>T , CM000663.2:g.25809097A>T	GRCh38
NC_000001.10:g.26135588A>T , CM000663.1:g.26135588A>T	GRCh37
NC_000001.9:g.26008175A>T	NCBI36
NG_009930.1:g.13922A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000354177.9:c.648A>T	ENSP00000346109.5:p.Gly216=
ENST00000494537.2:c.717A>T	ENSP00000508308.1:p.Gly239=
ENST00000361547.7:c.819A>T MANE Select	ENSP00000355141.2:p.Gly273=
ENST00000354177.8:c.717A>T	ENSP00000346109.4:p.Gly239=
ENST00000361547.6:c.819A>T	ENSP00000355141.2:p.Gly273=
ENST00000374315.1:c.717A>T	ENSP00000363434.1:p.Gly239=
NM_020451.2:c.819A>T	NP_065184.2:p.Gly273=
NM_206926.1:c.717A>T	NP_996809.1:p.Gly239=
NM_020451.3:c.819A>T MANE Select	NP_065184.2:p.Gly273=
NM_206926.2:c.717A>T	NP_996809.1:p.Gly239=