Canonical Allele Identifier: CA1159806127
Gene: SELENON HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.25809022C= , CM000663.2:g.25809022C= GRCh38
NC_000001.10:g.26135513C= , CM000663.1:g.26135513C= GRCh37
NC_000001.9:g.26008100C= NCBI36
NG_009930.1:g.13847C=

Transcript Alleles

HGVS Amino-acid change
ENST00000354177.9:c.646-73C= ENSP00000346109.5:n.646-73C=
ENST00000494537.2:c.646-4C= ENSP00000508308.1:n.646-4C=
ENST00000361547.7:c.748-4C= MANE Select ENSP00000355141.2:n.748-4C=
ENST00000354177.8:c.646-4C= ENSP00000346109.4:n.646-4C=
ENST00000361547.6:c.748-4C= ENSP00000355141.2:n.748-4C=
ENST00000374315.1:c.646-4C= ENSP00000363434.1:n.646-4C=
NM_020451.2:c.748-4C= NP_065184.2:n.748-4C=
NM_206926.1:c.646-4C= NP_996809.1:n.646-4C=
NM_020451.3:c.748-4C= MANE Select NP_065184.2:n.748-4C=
NM_206926.2:c.646-4C= NP_996809.1:n.646-4C=
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