Canonical Allele Identifier: CA999748075
Gene: SELENON HGNC NCBI

Linked Data

dbSNP Id: rs2047974405

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.25812606_25812607insACAAACACACACACACAC , CM000663.2:g.25812606_25812607insACAAACACACACACACAC GRCh38
NC_000001.10:g.26139097_26139098insACAAACACACACACACAC , CM000663.1:g.26139097_26139098insACAAACACACACACACAC GRCh37
NC_000001.9:g.26011684_26011685insACAAACACACACACACAC NCBI36
NG_009930.1:g.17431_17432insACAAACACACACACACAC

Transcript Alleles

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