Canonical Allele Identifier: CA734443704

Gene: SELENON

Linked Data

• dbSNP Id: rs1437406296
• gnomAD v3: 1-25812672-T-G
• gnomAD v4: 1-25812672-T-G
• MyVariant Identifiers: chr1:g.26139163T>G (hg19) ; chr1:g.25812672T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25812672T>G , CM000663.2:g.25812672T>G	GRCh38
NC_000001.10:g.26139163T>G , CM000663.1:g.26139163T>G	GRCh37
NC_000001.9:g.26011750T>G	NCBI36
NG_009930.1:g.17497T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000354177.9:c.1111-15T>G	ENSP00000346109.5:n.1111-15T>G
ENST00000494537.2:c.1180-15T>G	ENSP00000508308.1:n.1180-15T>G
ENST00000361547.7:c.1282-15T>G MANE Select	ENSP00000355141.2:n.1282-15T>G
ENST00000354177.8:c.1180-15T>G	ENSP00000346109.4:n.1180-15T>G
ENST00000361547.6:c.1282-15T>G	ENSP00000355141.2:n.1282-15T>G
ENST00000374315.1:c.1180-15T>G	ENSP00000363434.1:n.1180-15T>G
ENST00000559265.1:n.255+793T>G
NM_020451.2:c.1282-15T>G	NP_065184.2:n.1282-15T>G
NM_206926.1:c.1180-15T>G	NP_996809.1:n.1180-15T>G
NM_020451.3:c.1282-15T>G MANE Select	NP_065184.2:n.1282-15T>G
NM_206926.2:c.1180-15T>G	NP_996809.1:n.1180-15T>G