Canonical Allele Identifier: CA521739549

Gene: SELENON

Linked Data

• dbSNP Id: rs1296283028
• gnomAD v2: 1-26139093-C-CACACACACACACACAA
• MyVariant Identifiers: chr1:g.26139093_26139094insACACACACACACACAA (hg19) ; chr1:g.25812602_25812603insACACACACACACACAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25812606_25812607insACACACACACAAACAC , CM000663.2:g.25812606_25812607insACACACACACAAACAC	GRCh38
NC_000001.10:g.26139097_26139098insACACACACACAAACAC , CM000663.1:g.26139097_26139098insACACACACACAAACAC	GRCh37
NC_000001.9:g.26011684_26011685insACACACACACAAACAC	NCBI36
NG_009930.1:g.17431_17432insACACACACACAAACAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354177.9:c.1111-81_1111-80insACACACACACAAACAC	ENSP00000346109.5:n.1111-81_1111-80insACACACACACAAACAC
ENST00000494537.2:c.1180-81_1180-80insACACACACACAAACAC	ENSP00000508308.1:n.1180-81_1180-80insACACACACACAAACAC
ENST00000361547.7:c.1282-81_1282-80insACACACACACAAACAC MANE Select	ENSP00000355141.2:n.1282-81_1282-80insACACACACACAAACAC
ENST00000354177.8:c.1180-81_1180-80insACACACACACAAACAC	ENSP00000346109.4:n.1180-81_1180-80insACACACACACAAACAC
ENST00000361547.6:c.1282-81_1282-80insACACACACACAAACAC	ENSP00000355141.2:n.1282-81_1282-80insACACACACACAAACAC
ENST00000374315.1:c.1180-81_1180-80insACACACACACAAACAC	ENSP00000363434.1:n.1180-81_1180-80insACACACACACAAACAC
ENST00000559265.1:n.255+727_255+728insACACACACACAAACAC
NM_020451.2:c.1282-81_1282-80insACACACACACAAACAC	NP_065184.2:n.1282-81_1282-80insACACACACACAAACAC
NM_206926.1:c.1180-81_1180-80insACACACACACAAACAC	NP_996809.1:n.1180-81_1180-80insACACACACACAAACAC
NM_020451.3:c.1282-81_1282-80insACACACACACAAACAC MANE Select	NP_065184.2:n.1282-81_1282-80insACACACACACAAACAC
NM_206926.2:c.1180-81_1180-80insACACACACACAAACAC	NP_996809.1:n.1180-81_1180-80insACACACACACAAACAC