Canonical Allele Identifier: CA734440914

Gene: SELENON

Linked Data

• dbSNP Id: rs1477649472
• gnomAD v3: 1-25809281-GCTCT-G
• gnomAD v4: 1-25809281-GCTCT-G
• MyVariant Identifiers: chr1:g.26135773_26135776del (hg19) ; chr1:g.25809282_25809285del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25809284_25809287del , CM000663.2:g.25809284_25809287del	GRCh38
NC_000001.10:g.26135775_26135778del , CM000663.1:g.26135775_26135778del	GRCh37
NC_000001.9:g.26008362_26008365del	NCBI36
NG_009930.1:g.14109_14112del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354177.9:c.701+134_701+137del	ENSP00000346109.5:n.701+134_701+137del
ENST00000494537.2:c.770+134_770+137del	ENSP00000508308.1:n.770+134_770+137del
ENST00000361547.7:c.872+134_872+137del MANE Select	ENSP00000355141.2:n.872+134_872+137del
ENST00000354177.8:c.770+134_770+137del	ENSP00000346109.4:n.770+134_770+137del
ENST00000361547.6:c.872+134_872+137del	ENSP00000355141.2:n.872+134_872+137del
ENST00000374315.1:c.770+134_770+137del	ENSP00000363434.1:n.770+134_770+137del
NM_020451.2:c.872+134_872+137del	NP_065184.2:n.872+134_872+137del
NM_206926.1:c.770+134_770+137del	NP_996809.1:n.770+134_770+137del
NM_020451.3:c.872+134_872+137del MANE Select	NP_065184.2:n.872+134_872+137del
NM_206926.2:c.770+134_770+137del	NP_996809.1:n.770+134_770+137del