Canonical Allele Identifier: CA1159807866

Gene: SELENON

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25812694A= , CM000663.2:g.25812694A=	GRCh38
NC_000001.10:g.26139185A= , CM000663.1:g.26139185A=	GRCh37
NC_000001.9:g.26011772A=	NCBI36
NG_009930.1:g.17519A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000354177.9:c.1118A=	ENSP00000346109.5:p.Tyr373=
ENST00000494537.2:c.1187A=	ENSP00000508308.1:p.Tyr396=
ENST00000361547.7:c.1289A= MANE Select	ENSP00000355141.2:p.Tyr430=
ENST00000354177.8:c.1187A=	ENSP00000346109.4:p.Tyr396=
ENST00000361547.6:c.1289A=	ENSP00000355141.2:p.Tyr430=
ENST00000374315.1:c.1187A=	ENSP00000363434.1:p.Tyr396=
ENST00000559265.1:n.255+815A=
ENST00000630065.2:c.-284A=	ENSP00000487549.1:n.-284A=
NM_020451.2:c.1289A=	NP_065184.2:p.Tyr430=
NM_206926.1:c.1187A=	NP_996809.1:p.Tyr396=
NM_020451.3:c.1289A= MANE Select	NP_065184.2:p.Tyr430=
NM_206926.2:c.1187A=	NP_996809.1:p.Tyr396=