Canonical Allele Identifier: CA521739554

Gene: SELENON

Linked Data

• dbSNP Id: rs1220156384
• gnomAD v2: 1-26139096-ACTTG-A
• gnomAD v3: 1-25812605-ACTTG-A
• gnomAD v4: 1-25812605-ACTTG-A
• MyVariant Identifiers: chr1:g.26139097_26139100del (hg19) ; chr1:g.25812606_25812609del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25812607_25812610del , CM000663.2:g.25812607_25812610del	GRCh38
NC_000001.10:g.26139098_26139101del , CM000663.1:g.26139098_26139101del	GRCh37
NC_000001.9:g.26011685_26011688del	NCBI36
NG_009930.1:g.17432_17435del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354177.9:c.1111-80_1111-77del	ENSP00000346109.5:n.1111-80_1111-77del
ENST00000494537.2:c.1180-80_1180-77del	ENSP00000508308.1:n.1180-80_1180-77del
ENST00000361547.7:c.1282-80_1282-77del MANE Select	ENSP00000355141.2:n.1282-80_1282-77del
ENST00000354177.8:c.1180-80_1180-77del	ENSP00000346109.4:n.1180-80_1180-77del
ENST00000361547.6:c.1282-80_1282-77del	ENSP00000355141.2:n.1282-80_1282-77del
ENST00000374315.1:c.1180-80_1180-77del	ENSP00000363434.1:n.1180-80_1180-77del
ENST00000559265.1:n.255+728_255+731del
NM_020451.2:c.1282-80_1282-77del	NP_065184.2:n.1282-80_1282-77del
NM_206926.1:c.1180-80_1180-77del	NP_996809.1:n.1180-80_1180-77del
NM_020451.3:c.1282-80_1282-77del MANE Select	NP_065184.2:n.1282-80_1282-77del
NM_206926.2:c.1180-80_1180-77del	NP_996809.1:n.1180-80_1180-77del