Canonical Allele Identifier: CA734443435

Gene: SELENON

Linked Data

• dbSNP Id: rs59333545
• gnomAD v3: 1-25812564-A-AACACACACACACAC
• gnomAD v4: 1-25812564-A-AACACACACACACAC
• MyVariant Identifiers: chr1:g.26139055_26139056insACACACACACACAC (hg19) ; chr1:g.25812564_25812565insACACACACACACAC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25812593_25812606dup , CM000663.2:g.25812593_25812606dup	GRCh38
NC_000001.10:g.26139084_26139097dup , CM000663.1:g.26139084_26139097dup	GRCh37
NC_000001.9:g.26011671_26011684dup	NCBI36
NG_009930.1:g.17418_17431dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354177.9:c.1111-94_1111-81dup	ENSP00000346109.5:n.1111-94_1111-81dup
ENST00000494537.2:c.1180-94_1180-81dup	ENSP00000508308.1:n.1180-94_1180-81dup
ENST00000361547.7:c.1282-94_1282-81dup MANE Select	ENSP00000355141.2:n.1282-94_1282-81dup
ENST00000354177.8:c.1180-94_1180-81dup	ENSP00000346109.4:n.1180-94_1180-81dup
ENST00000361547.6:c.1282-94_1282-81dup	ENSP00000355141.2:n.1282-94_1282-81dup
ENST00000374315.1:c.1180-94_1180-81dup	ENSP00000363434.1:n.1180-94_1180-81dup
ENST00000559265.1:n.255+714_255+727dup
NM_020451.2:c.1282-94_1282-81dup	NP_065184.2:n.1282-94_1282-81dup
NM_206926.1:c.1180-94_1180-81dup	NP_996809.1:n.1180-94_1180-81dup
NM_020451.3:c.1282-94_1282-81dup MANE Select	NP_065184.2:n.1282-94_1282-81dup
NM_206926.2:c.1180-94_1180-81dup	NP_996809.1:n.1180-94_1180-81dup