Canonical Allele Identifier: CA1141580680

Gene: SELENON

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25809096G= , CM000663.2:g.25809096G=	GRCh38
NC_000001.10:g.26135587G= , CM000663.1:g.26135587G=	GRCh37
NC_000001.9:g.26008174G=	NCBI36
NG_009930.1:g.13921G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000354177.9:c.647G=	ENSP00000346109.5:p.Gly216=
ENST00000494537.2:c.716G=	ENSP00000508308.1:p.Gly239=
ENST00000361547.7:c.818G= MANE Select	ENSP00000355141.2:p.Gly273=
ENST00000354177.8:c.716G=	ENSP00000346109.4:p.Gly239=
ENST00000361547.6:c.818G=	ENSP00000355141.2:p.Gly273=
ENST00000374315.1:c.716G=	ENSP00000363434.1:p.Gly239=
NM_020451.2:c.818G=	NP_065184.2:p.Gly273=
NM_206926.1:c.716G=	NP_996809.1:p.Gly239=
NM_020451.3:c.818G= MANE Select	NP_065184.2:p.Gly273=
NM_206926.2:c.716G=	NP_996809.1:p.Gly239=