Canonical Allele Identifier: CA253172
Community Standard Title: NM_020451.3(SELENON):c.713dup (p.Asn238LysfsTer?)
Gene: SELENON HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.25808755dup , CM000663.2:g.25808755dup GRCh38
NC_000001.10:g.26135246dup , CM000663.1:g.26135246dup GRCh37
NC_000001.9:g.26007833dup NCBI36
NG_009930.1:g.13580dup

Transcript Alleles

HGVS Amino-acid Change
NM_020451.3:c.713dup MANE Select NP_065184.2:p.Asn238LysfsTer?
ENST00000361547.7:c.713dup MANE Select ENSP00000355141.2:p.Asn238LysfsTer?
NM_020451.2:c.713dup NP_065184.2:p.Asn238LysfsTer?
NM_206926.1:c.611dup NP_996809.1:p.Asn204LysfsTer?
NM_206926.2:c.611dup NP_996809.1:p.Asn204LysfsTer?
ENST00000354177.8:c.611dup ENSP00000346109.4:p.Asn204LysfsTer?
ENST00000354177.9:c.611dup ENSP00000346109.5:p.Asn204LysfsTer?
ENST00000361547.6:c.713dup ENSP00000355141.2:p.Asn238LysfsTer?
ENST00000374315.1:c.611dup ENSP00000363434.1:p.Asn204LysfsTer?
ENST00000494537.2:c.611dup ENSP00000508308.1:p.Asn204LysfsTer?
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