Canonical Allele Identifier: CA696871

Gene: SELENON

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25813889C>T , CM000663.2:g.25813889C>T	GRCh38
NC_000001.10:g.26140380C>T , CM000663.1:g.26140380C>T	GRCh37
NC_000001.9:g.26012967C>T	NCBI36
NG_009930.1:g.18714C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_020451.3:c.1396C>T MANE Select	NP_065184.2:p.Arg466Trp
ENST00000361547.7:c.1396C>T MANE Select	ENSP00000355141.2:p.Arg466Trp
NM_020451.2:c.1396C>T	NP_065184.2:p.Arg466Trp
NM_206926.1:c.1294C>T	NP_996809.1:p.Arg432Trp
NM_206926.2:c.1294C>T	NP_996809.1:p.Arg432Trp
ENST00000354177.8:c.1294C>T	ENSP00000346109.4:p.Arg432Trp
ENST00000354177.9:c.1225C>T	ENSP00000346109.5:p.Arg409Trp
ENST00000361547.6:c.1396C>T	ENSP00000355141.2:p.Arg466Trp
ENST00000374315.1:c.1294C>T	ENSP00000363434.1:p.Arg432Trp
ENST00000494537.1:n.163C>T
ENST00000494537.2:c.1383C>T	ENSP00000508308.1:p.Gly461=
ENST00000559265.1:n.255+2010C>T
ENST00000630065.2:c.-177C>T	ENSP00000487549.1:n.-177C>T