Canonical Allele Identifier: CA1159807890

Gene: SELENON

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25812764G= , CM000663.2:g.25812764G=	GRCh38
NC_000001.10:g.26139255G= , CM000663.1:g.26139255G=	GRCh37
NC_000001.9:g.26011842G=	NCBI36
NG_009930.1:g.17589G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000354177.9:c.1188G=	ENSP00000346109.5:p.Trp396=
ENST00000494537.2:c.1257G=	ENSP00000508308.1:p.Trp419=
ENST00000361547.7:c.1359G= MANE Select	ENSP00000355141.2:p.Trp453=
ENST00000354177.8:c.1257G=	ENSP00000346109.4:p.Trp419=
ENST00000361547.6:c.1359G=	ENSP00000355141.2:p.Trp453=
ENST00000374315.1:c.1257G=	ENSP00000363434.1:p.Trp419=
ENST00000494537.1:n.37G=
ENST00000559265.1:n.255+885G=
ENST00000630065.2:c.-214G=	ENSP00000487549.1:n.-214G=
NM_020451.2:c.1359G=	NP_065184.2:p.Trp453=
NM_206926.1:c.1257G=	NP_996809.1:p.Trp419=
NM_020451.3:c.1359G= MANE Select	NP_065184.2:p.Trp453=
NM_206926.2:c.1257G=	NP_996809.1:p.Trp419=