Canonical Allele Identifier: CA2644199796

Gene: SELENON

Linked Data

• gnomAD v4: 1-25809220-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25809220_25809221insT , CM000663.2:g.25809220_25809221insT	GRCh38
NC_000001.10:g.26135711_26135712insT , CM000663.1:g.26135711_26135712insT	GRCh37
NC_000001.9:g.26008298_26008299insT	NCBI36
NG_009930.1:g.14045_14046insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354177.9:c.701+70_701+71insT	ENSP00000346109.5:n.701+70_701+71insT
ENST00000494537.2:c.770+70_770+71insT	ENSP00000508308.1:n.770+70_770+71insT
ENST00000361547.7:c.872+70_872+71insT MANE Select	ENSP00000355141.2:n.872+70_872+71insT
ENST00000354177.8:c.770+70_770+71insT	ENSP00000346109.4:n.770+70_770+71insT
ENST00000361547.6:c.872+70_872+71insT	ENSP00000355141.2:n.872+70_872+71insT
ENST00000374315.1:c.770+70_770+71insT	ENSP00000363434.1:n.770+70_770+71insT
NM_020451.2:c.872+70_872+71insT	NP_065184.2:n.872+70_872+71insT
NM_206926.1:c.770+70_770+71insT	NP_996809.1:n.770+70_770+71insT
NM_020451.3:c.872+70_872+71insT MANE Select	NP_065184.2:n.872+70_872+71insT
NM_206926.2:c.770+70_770+71insT	NP_996809.1:n.770+70_770+71insT