Canonical Allele Identifier: CA1159807892

Gene: SELENON

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25812769C= , CM000663.2:g.25812769C=	GRCh38
NC_000001.10:g.26139260C= , CM000663.1:g.26139260C=	GRCh37
NC_000001.9:g.26011847C=	NCBI36
NG_009930.1:g.17594C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000354177.9:c.1193C=	ENSP00000346109.5:p.Ala398=
ENST00000494537.2:c.1262C=	ENSP00000508308.1:p.Ala421=
ENST00000361547.7:c.1364C= MANE Select	ENSP00000355141.2:p.Ala455=
ENST00000354177.8:c.1262C=	ENSP00000346109.4:p.Ala421=
ENST00000361547.6:c.1364C=	ENSP00000355141.2:p.Ala455=
ENST00000374315.1:c.1262C=	ENSP00000363434.1:p.Ala421=
ENST00000494537.1:n.42C=
ENST00000559265.1:n.255+890C=
ENST00000630065.2:c.-209C=	ENSP00000487549.1:n.-209C=
NM_020451.2:c.1364C=	NP_065184.2:p.Ala455=
NM_206926.1:c.1262C=	NP_996809.1:p.Ala421=
NM_020451.3:c.1364C= MANE Select	NP_065184.2:p.Ala455=
NM_206926.2:c.1262C=	NP_996809.1:p.Ala421=