Canonical Allele Identifier: CA1159806124
Gene: SELENON HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.25809019C= , CM000663.2:g.25809019C= GRCh38
NC_000001.10:g.26135510C= , CM000663.1:g.26135510C= GRCh37
NC_000001.9:g.26008097C= NCBI36
NG_009930.1:g.13844C=

Transcript Alleles

HGVS Amino-acid change
ENST00000354177.9:c.646-76C= ENSP00000346109.5:n.646-76C=
ENST00000494537.2:c.646-7C= ENSP00000508308.1:n.646-7C=
ENST00000361547.7:c.748-7C= MANE Select ENSP00000355141.2:n.748-7C=
ENST00000354177.8:c.646-7C= ENSP00000346109.4:n.646-7C=
ENST00000361547.6:c.748-7C= ENSP00000355141.2:n.748-7C=
ENST00000374315.1:c.646-7C= ENSP00000363434.1:n.646-7C=
NM_020451.2:c.748-7C= NP_065184.2:n.748-7C=
NM_206926.1:c.646-7C= NP_996809.1:n.646-7C=
NM_020451.3:c.748-7C= MANE Select NP_065184.2:n.748-7C=
NM_206926.2:c.646-7C= NP_996809.1:n.646-7C=
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