Canonical Allele Identifier: CA696963

Gene: SELENON

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25815583C>T , CM000663.2:g.25815583C>T	GRCh38
NC_000001.10:g.26142074C>T , CM000663.1:g.26142074C>T	GRCh37
NC_000001.9:g.26014661C>T	NCBI36
NG_009930.1:g.20408C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354177.9:c.1467C>T	ENSP00000346109.5:p.Ile489=
ENST00000494537.2:c.1625C>T	ENSP00000508308.1:n.1625C>T
ENST00000361547.7:c.1638C>T MANE Select	ENSP00000355141.2:p.Ile546=
ENST00000354177.8:c.1536C>T	ENSP00000346109.4:p.Ile512=
ENST00000361547.6:c.1638C>T	ENSP00000355141.2:p.Ile546=
ENST00000374315.1:c.1536C>T	ENSP00000363434.1:p.Ile512=
ENST00000494537.1:n.405C>T
ENST00000527604.1:c.123+1405C>T	ENSP00000457066.1:n.123+1405C>T
ENST00000559265.1:n.255+3704C>T
ENST00000630065.2:c.66C>T	ENSP00000487549.1:p.Ile22=
NM_020451.2:c.1638C>T	NP_065184.2:p.Ile546=
NM_206926.1:c.1536C>T	NP_996809.1:p.Ile512=
NM_020451.3:c.1638C>T MANE Select	NP_065184.2:p.Ile546=
NM_206926.2:c.1536C>T	NP_996809.1:p.Ile512=