Canonical Allele Identifier: CA1159806217
Gene: SELENON HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.25809252C= , CM000663.2:g.25809252C= GRCh38
NC_000001.10:g.26135743C= , CM000663.1:g.26135743C= GRCh37
NC_000001.9:g.26008330C= NCBI36
NG_009930.1:g.14077C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000354177.9:c.701+102C= ENSP00000346109.5:n.701+102C=
ENST00000494537.2:c.770+102C= ENSP00000508308.1:n.770+102C=
ENST00000361547.7:c.872+102C= MANE Select ENSP00000355141.2:n.872+102C=
ENST00000354177.8:c.770+102C= ENSP00000346109.4:n.770+102C=
ENST00000361547.6:c.872+102C= ENSP00000355141.2:n.872+102C=
ENST00000374315.1:c.770+102C= ENSP00000363434.1:n.770+102C=
NM_020451.2:c.872+102C= NP_065184.2:n.872+102C=
NM_206926.1:c.770+102C= NP_996809.1:n.770+102C=
NM_020451.3:c.872+102C= MANE Select NP_065184.2:n.872+102C=
NM_206926.2:c.770+102C= NP_996809.1:n.770+102C=
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