Canonical Allele Identifier: CA416759334

Gene: SELENON

Linked Data

• MyVariant Identifiers: chr1:g.26140382G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25813891G>C , CM000663.2:g.25813891G>C	GRCh38
NC_000001.10:g.26140382G>C , CM000663.1:g.26140382G>C	GRCh37
NC_000001.9:g.26012969G>C	NCBI36
NG_009930.1:g.18716G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000354177.9:c.1227G>C	ENSP00000346109.5:p.Arg409=
ENST00000494537.2:c.1385G>C	ENSP00000508308.1:p.Gly462Ala
ENST00000361547.7:c.1398G>C MANE Select	ENSP00000355141.2:p.Arg466=
ENST00000354177.8:c.1296G>C	ENSP00000346109.4:p.Arg432=
ENST00000361547.6:c.1398G>C	ENSP00000355141.2:p.Arg466=
ENST00000374315.1:c.1296G>C	ENSP00000363434.1:p.Arg432=
ENST00000494537.1:n.165G>C
ENST00000559265.1:n.255+2012G>C
ENST00000630065.2:c.-175G>C	ENSP00000487549.1:n.-175G>C
NM_020451.2:c.1398G>C	NP_065184.2:p.Arg466=
NM_206926.1:c.1296G>C	NP_996809.1:p.Arg432=
NM_020451.3:c.1398G>C MANE Select	NP_065184.2:p.Arg466=
NM_206926.2:c.1296G>C	NP_996809.1:p.Arg432=