Canonical Allele Identifier: CA2695675607

Gene: SELENON

Linked Data

• dbSNP Id: rs2124447888

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25809000del , CM000663.2:g.25809000del	GRCh38
NC_000001.10:g.26135491del , CM000663.1:g.26135491del	GRCh37
NC_000001.9:g.26008078del	NCBI36
NG_009930.1:g.13825del

Transcript Alleles

HGVS	Amino-acid change
ENST00000354177.9:c.646-95del	ENSP00000346109.5:n.646-95del
ENST00000494537.2:c.646-26del	ENSP00000508308.1:n.646-26del
ENST00000361547.7:c.748-26del MANE Select	ENSP00000355141.2:n.748-26del
ENST00000354177.8:c.646-26del	ENSP00000346109.4:n.646-26del
ENST00000361547.6:c.748-26del	ENSP00000355141.2:n.748-26del
ENST00000374315.1:c.646-26del	ENSP00000363434.1:n.646-26del
NM_020451.2:c.748-26del	NP_065184.2:n.748-26del
NM_206926.1:c.646-26del	NP_996809.1:n.646-26del
NM_020451.3:c.748-26del MANE Select	NP_065184.2:n.748-26del
NM_206926.2:c.646-26del	NP_996809.1:n.646-26del