Canonical Allele Identifier: CA696969

Gene: SELENON

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25815649G>A , CM000663.2:g.25815649G>A	GRCh38
NC_000001.10:g.26142140G>A , CM000663.1:g.26142140G>A	GRCh37
NC_000001.9:g.26014727G>A	NCBI36
NG_009930.1:g.20474G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354177.9:c.1533G>A	ENSP00000346109.5:p.Pro511=
ENST00000494537.2:c.1691G>A	ENSP00000508308.1:n.1691G>A
ENST00000361547.7:c.1704G>A MANE Select	ENSP00000355141.2:p.Pro568=
ENST00000354177.8:c.1602G>A	ENSP00000346109.4:p.Pro534=
ENST00000361547.6:c.1704G>A	ENSP00000355141.2:p.Pro568=
ENST00000374315.1:c.1602G>A	ENSP00000363434.1:p.Pro534=
ENST00000494537.1:n.471G>A
ENST00000527604.1:c.123+1471G>A	ENSP00000457066.1:n.123+1471G>A
ENST00000559265.1:n.255+3770G>A
ENST00000630065.2:c.132G>A	ENSP00000487549.1:p.Pro44=
NM_020451.2:c.1704G>A	NP_065184.2:p.Pro568=
NM_206926.1:c.1602G>A	NP_996809.1:p.Pro534=
NM_020451.3:c.1704G>A MANE Select	NP_065184.2:p.Pro568=
NM_206926.2:c.1602G>A	NP_996809.1:p.Pro534=