Canonical Allele Identifier: CA1141096141

Gene: SELENON

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25809033T= , CM000663.2:g.25809033T=	GRCh38
NC_000001.10:g.26135524T= , CM000663.1:g.26135524T=	GRCh37
NC_000001.9:g.26008111T=	NCBI36
NG_009930.1:g.13858T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354177.9:c.646-62T=	ENSP00000346109.5:n.646-62T=
ENST00000494537.2:c.653T=	ENSP00000508308.1:p.Ile218=
ENST00000361547.7:c.755T= MANE Select	ENSP00000355141.2:p.Ile252=
ENST00000354177.8:c.653T=	ENSP00000346109.4:p.Ile218=
ENST00000361547.6:c.755T=	ENSP00000355141.2:p.Ile252=
ENST00000374315.1:c.653T=	ENSP00000363434.1:p.Ile218=
NM_020451.2:c.755T=	NP_065184.2:p.Ile252=
NM_206926.1:c.653T=	NP_996809.1:p.Ile218=
NM_020451.3:c.755T= MANE Select	NP_065184.2:p.Ile252=
NM_206926.2:c.653T=	NP_996809.1:p.Ile218=