Canonical Allele Identifier: CA19698939
Gene: SELENON HGNC NCBI

Linked Data

dbSNP Id: rs121908183
MyVariant Identifiers: chr1:g.26139280_26139282del (hg19) chr1:g.25812789_25812791del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.25812789_25812791del , CM000663.2:g.25812789_25812791del GRCh38
NC_000001.10:g.26139280_26139282del , CM000663.1:g.26139280_26139282del GRCh37
NC_000001.9:g.26011867_26011869del NCBI36
NG_009930.1:g.17614_17616del

Transcript Alleles

HGVS Amino-acid change
ENST00000354177.9:c.1213_1215del ENSP00000346109.5:p.Ter405del
ENST00000494537.2:c.1282_1284del ENSP00000508308.1:p.Ter428del
ENST00000361547.7:c.1384_1386del MANE Select ENSP00000355141.2:p.Ter462del
ENST00000354177.8:c.1274+8_1274+10del ENSP00000346109.4:n.1274+8_1274+10del
ENST00000361547.6:c.1384_1386del ENSP00000355141.2:p.Ter462del
ENST00000374315.1:c.1282_1284del ENSP00000363434.1:p.Ter428del
ENST00000494537.1:n.62_64del
ENST00000559265.1:n.255+910_255+912del
ENST00000630065.2:c.-189_-187del ENSP00000487549.1:n.-189_-187del
NM_020451.2:c.1384_1386del NP_065184.2:p.Ter462del
NM_206926.1:c.1282_1284del NP_996809.1:p.Ter428del
NM_020451.3:c.1384_1386del MANE Select NP_065184.2:p.Ter462del
NM_206926.2:c.1282_1284del NP_996809.1:p.Ter428del
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