Canonical Allele Identifier: CA734440960

Gene: SELENON

Linked Data

• dbSNP Id: rs1159156206
• MyVariant Identifiers: chr1:g.26135909G>A (hg19) ; chr1:g.25809418G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25809418G>A , CM000663.2:g.25809418G>A	GRCh38
NC_000001.10:g.26135909G>A , CM000663.1:g.26135909G>A	GRCh37
NC_000001.9:g.26008496G>A	NCBI36
NG_009930.1:g.14243G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354177.9:c.702-265G>A	ENSP00000346109.5:n.702-265G>A
ENST00000494537.2:c.771-265G>A	ENSP00000508308.1:n.771-265G>A
ENST00000361547.7:c.873-265G>A MANE Select	ENSP00000355141.2:n.873-265G>A
ENST00000354177.8:c.771-265G>A	ENSP00000346109.4:n.771-265G>A
ENST00000361547.6:c.873-265G>A	ENSP00000355141.2:n.873-265G>A
ENST00000374315.1:c.771-265G>A	ENSP00000363434.1:n.771-265G>A
NM_020451.2:c.873-265G>A	NP_065184.2:n.873-265G>A
NM_206926.1:c.771-265G>A	NP_996809.1:n.771-265G>A
NM_020451.3:c.873-265G>A MANE Select	NP_065184.2:n.873-265G>A
NM_206926.2:c.771-265G>A	NP_996809.1:n.771-265G>A