Canonical Allele Identifier: CA19698449

Gene: SELENON

Linked Data

• dbSNP Id: rs778070283
• MyVariant Identifiers: chr1:g.26135795_26135796insC (hg19) ; chr1:g.25809304_25809305insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25809306dup , CM000663.2:g.25809306dup	GRCh38
NC_000001.10:g.26135797dup , CM000663.1:g.26135797dup	GRCh37
NC_000001.9:g.26008384dup	NCBI36
NG_009930.1:g.14131dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354177.9:c.701+156dup	ENSP00000346109.5:n.701+156dup
ENST00000494537.2:c.770+156dup	ENSP00000508308.1:n.770+156dup
ENST00000361547.7:c.872+156dup MANE Select	ENSP00000355141.2:n.872+156dup
ENST00000354177.8:c.770+156dup	ENSP00000346109.4:n.770+156dup
ENST00000361547.6:c.872+156dup	ENSP00000355141.2:n.872+156dup
ENST00000374315.1:c.770+156dup	ENSP00000363434.1:n.770+156dup
NM_020451.2:c.872+156dup	NP_065184.2:n.872+156dup
NM_206926.1:c.770+156dup	NP_996809.1:n.770+156dup
NM_020451.3:c.872+156dup MANE Select	NP_065184.2:n.872+156dup
NM_206926.2:c.770+156dup	NP_996809.1:n.770+156dup