Canonical Allele Identifier: CA999746488

Gene: SELENON

Linked Data

• dbSNP Id: rs2047937756
• gnomAD v3: 1-25809288-G-GA
• gnomAD v4: 1-25809288-G-GA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25809289dup , CM000663.2:g.25809289dup	GRCh38
NC_000001.10:g.26135780dup , CM000663.1:g.26135780dup	GRCh37
NC_000001.9:g.26008367dup	NCBI36
NG_009930.1:g.14114dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354177.9:c.701+139dup	ENSP00000346109.5:n.701+139dup
ENST00000494537.2:c.770+139dup	ENSP00000508308.1:n.770+139dup
ENST00000361547.7:c.872+139dup MANE Select	ENSP00000355141.2:n.872+139dup
ENST00000354177.8:c.770+139dup	ENSP00000346109.4:n.770+139dup
ENST00000361547.6:c.872+139dup	ENSP00000355141.2:n.872+139dup
ENST00000374315.1:c.770+139dup	ENSP00000363434.1:n.770+139dup
NM_020451.2:c.872+139dup	NP_065184.2:n.872+139dup
NM_206926.1:c.770+139dup	NP_996809.1:n.770+139dup
NM_020451.3:c.872+139dup MANE Select	NP_065184.2:n.872+139dup
NM_206926.2:c.770+139dup	NP_996809.1:n.770+139dup