Canonical Allele Identifier: CA734443560

Gene: SELENON

Linked Data

• dbSNP Id: rs1255886229
• gnomAD v3: 1-25812591-ACACACACACACAC-A
• gnomAD v4: 1-25812591-ACACACACACACAC-A
• MyVariant Identifiers: chr1:g.26139083_26139095del (hg19) ; chr1:g.25812592_25812604del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25812592_25812604del , CM000663.2:g.25812592_25812604del	GRCh38
NC_000001.10:g.26139083_26139095del , CM000663.1:g.26139083_26139095del	GRCh37
NC_000001.9:g.26011670_26011682del	NCBI36
NG_009930.1:g.17417_17429del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354177.9:c.1111-95_1111-83del	ENSP00000346109.5:n.1111-95_1111-83del
ENST00000494537.2:c.1180-95_1180-83del	ENSP00000508308.1:n.1180-95_1180-83del
ENST00000361547.7:c.1282-95_1282-83del MANE Select	ENSP00000355141.2:n.1282-95_1282-83del
ENST00000354177.8:c.1180-95_1180-83del	ENSP00000346109.4:n.1180-95_1180-83del
ENST00000361547.6:c.1282-95_1282-83del	ENSP00000355141.2:n.1282-95_1282-83del
ENST00000374315.1:c.1180-95_1180-83del	ENSP00000363434.1:n.1180-95_1180-83del
ENST00000559265.1:n.255+713_255+725del
NM_020451.2:c.1282-95_1282-83del	NP_065184.2:n.1282-95_1282-83del
NM_206926.1:c.1180-95_1180-83del	NP_996809.1:n.1180-95_1180-83del
NM_020451.3:c.1282-95_1282-83del MANE Select	NP_065184.2:n.1282-95_1282-83del
NM_206926.2:c.1180-95_1180-83del	NP_996809.1:n.1180-95_1180-83del