Canonical Allele Identifier: CA645372407

Gene: SELENON

Linked Data

• ClinVar Variation Id: 432702
• ClinVar RCV Id: RCV000497682
• dbSNP Id: rs1553120678
• MyVariant Identifiers: chr1:g.26139185dup (hg19) ; chr1:g.25812694dup (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25812694dup , CM000663.2:g.25812694dup	GRCh38
NC_000001.10:g.26139185dup , CM000663.1:g.26139185dup	GRCh37
NC_000001.9:g.26011772dup	NCBI36
NG_009930.1:g.17519dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000354177.9:c.1118dup	ENSP00000346109.5:p.Tyr373Ter
ENST00000494537.2:c.1187dup	ENSP00000508308.1:p.Tyr396Ter
ENST00000361547.7:c.1289dup MANE Select	ENSP00000355141.2:p.Tyr430Ter
ENST00000354177.8:c.1187dup	ENSP00000346109.4:p.Tyr396Ter
ENST00000361547.6:c.1289dup	ENSP00000355141.2:p.Tyr430Ter
ENST00000374315.1:c.1187dup	ENSP00000363434.1:p.Tyr396Ter
ENST00000559265.1:n.255+815dup
ENST00000630065.2:c.-284dup	ENSP00000487549.1:n.-284dup
NM_020451.2:c.1289dup	NP_065184.2:p.Tyr430Ter
NM_206926.1:c.1187dup	NP_996809.1:p.Tyr396Ter
NM_020451.3:c.1289dup MANE Select	NP_065184.2:p.Tyr430Ter
NM_206926.2:c.1187dup	NP_996809.1:p.Tyr396Ter