Canonical Allele Identifier: CA696631
Gene: SELENON HGNC NCBI

Linked Data

ClinVar Variation Id: 1957395
ClinVar RCV Id: RCV002720494
dbSNP Id: rs763173485
ExAC: 1:26135506 G / A
gnomAD v2: 1-26135506-G-A
gnomAD v3: 1-25809015-G-A
gnomAD v4: 1-25809015-G-A
MyVariant Identifiers: chr1:g.26135506G>A (hg19) chr1:g.25809015G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.25809015G>A , CM000663.2:g.25809015G>A GRCh38
NC_000001.10:g.26135506G>A , CM000663.1:g.26135506G>A GRCh37
NC_000001.9:g.26008093G>A NCBI36
NG_009930.1:g.13840G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000354177.9:c.646-80G>A ENSP00000346109.5:n.646-80G>A
ENST00000494537.2:c.646-11G>A ENSP00000508308.1:n.646-11G>A
ENST00000361547.7:c.748-11G>A MANE Select ENSP00000355141.2:n.748-11G>A
ENST00000354177.8:c.646-11G>A ENSP00000346109.4:n.646-11G>A
ENST00000361547.6:c.748-11G>A ENSP00000355141.2:n.748-11G>A
ENST00000374315.1:c.646-11G>A ENSP00000363434.1:n.646-11G>A
NM_020451.2:c.748-11G>A NP_065184.2:n.748-11G>A
NM_206926.1:c.646-11G>A NP_996809.1:n.646-11G>A
NM_020451.3:c.748-11G>A MANE Select NP_065184.2:n.748-11G>A
NM_206926.2:c.646-11G>A NP_996809.1:n.646-11G>A
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