Canonical Allele Identifier: CA1144743687
Gene: SELENON HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.25809335G= , CM000663.2:g.25809335G= GRCh38
NC_000001.10:g.26135826G= , CM000663.1:g.26135826G= GRCh37
NC_000001.9:g.26008413G= NCBI36
NG_009930.1:g.14160G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000354177.9:c.701+185G= ENSP00000346109.5:n.701+185G=
ENST00000494537.2:c.770+185G= ENSP00000508308.1:n.770+185G=
ENST00000361547.7:c.872+185G= MANE Select ENSP00000355141.2:n.872+185G=
ENST00000354177.8:c.770+185G= ENSP00000346109.4:n.770+185G=
ENST00000361547.6:c.872+185G= ENSP00000355141.2:n.872+185G=
ENST00000374315.1:c.770+185G= ENSP00000363434.1:n.770+185G=
NM_020451.2:c.872+185G= NP_065184.2:n.872+185G=
NM_206926.1:c.770+185G= NP_996809.1:n.770+185G=
NM_020451.3:c.872+185G= MANE Select NP_065184.2:n.872+185G=
NM_206926.2:c.770+185G= NP_996809.1:n.770+185G=
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