Canonical Allele Identifier: CA10834691

Gene: SELENON

Linked Data

• ClinVar Variation Id: 1244808
• ClinVar RCV Id: RCV001649016
• dbSNP Id: rs2280997
• gnomAD v2: 1-26135741-C-G
• gnomAD v3: 1-25809250-C-G
• gnomAD v4: 1-25809250-C-G
• MyVariant Identifiers: chr1:g.26135741C>G (hg19) ; chr1:g.25809250C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25809250C>G , CM000663.2:g.25809250C>G	GRCh38
NC_000001.10:g.26135741C>G , CM000663.1:g.26135741C>G	GRCh37
NC_000001.9:g.26008328C>G	NCBI36
NG_009930.1:g.14075C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354177.9:c.701+100C>G	ENSP00000346109.5:n.701+100C>G
ENST00000494537.2:c.770+100C>G	ENSP00000508308.1:n.770+100C>G
ENST00000361547.7:c.872+100C>G MANE Select	ENSP00000355141.2:n.872+100C>G
ENST00000354177.8:c.770+100C>G	ENSP00000346109.4:n.770+100C>G
ENST00000361547.6:c.872+100C>G	ENSP00000355141.2:n.872+100C>G
ENST00000374315.1:c.770+100C>G	ENSP00000363434.1:n.770+100C>G
NM_020451.2:c.872+100C>G	NP_065184.2:n.872+100C>G
NM_206926.1:c.770+100C>G	NP_996809.1:n.770+100C>G
NM_020451.3:c.872+100C>G MANE Select	NP_065184.2:n.872+100C>G
NM_206926.2:c.770+100C>G	NP_996809.1:n.770+100C>G