Canonical Allele Identifier: CA416759312

Gene: SELENON

Linked Data

• MyVariant Identifiers: chr1:g.26139264G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25812773G>C , CM000663.2:g.25812773G>C	GRCh38
NC_000001.10:g.26139264G>C , CM000663.1:g.26139264G>C	GRCh37
NC_000001.9:g.26011851G>C	NCBI36
NG_009930.1:g.17598G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354177.9:c.1197G>C	ENSP00000346109.5:p.Leu399=
ENST00000494537.2:c.1266G>C	ENSP00000508308.1:p.Leu422=
ENST00000361547.7:c.1368G>C MANE Select	ENSP00000355141.2:p.Leu456=
ENST00000354177.8:c.1266G>C	ENSP00000346109.4:p.Leu422=
ENST00000361547.6:c.1368G>C	ENSP00000355141.2:p.Leu456=
ENST00000374315.1:c.1266G>C	ENSP00000363434.1:p.Leu422=
ENST00000494537.1:n.46G>C
ENST00000559265.1:n.255+894G>C
ENST00000630065.2:c.-205G>C	ENSP00000487549.1:n.-205G>C
NM_020451.2:c.1368G>C	NP_065184.2:p.Leu456=
NM_206926.1:c.1266G>C	NP_996809.1:p.Leu422=
NM_020451.3:c.1368G>C MANE Select	NP_065184.2:p.Leu456=
NM_206926.2:c.1266G>C	NP_996809.1:p.Leu422=