Canonical Allele Identifier: CA999748115

Gene: SELENON

Linked Data

• dbSNP Id: rs2047975031
• gnomAD v3: 1-25812607-TTG-T
• gnomAD v4: 1-25812607-TTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25812608_25812609del , CM000663.2:g.25812608_25812609del	GRCh38
NC_000001.10:g.26139099_26139100del , CM000663.1:g.26139099_26139100del	GRCh37
NC_000001.9:g.26011686_26011687del	NCBI36
NG_009930.1:g.17433_17434del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354177.9:c.1111-79_1111-78del	ENSP00000346109.5:n.1111-79_1111-78del
ENST00000494537.2:c.1180-79_1180-78del	ENSP00000508308.1:n.1180-79_1180-78del
ENST00000361547.7:c.1282-79_1282-78del MANE Select	ENSP00000355141.2:n.1282-79_1282-78del
ENST00000354177.8:c.1180-79_1180-78del	ENSP00000346109.4:n.1180-79_1180-78del
ENST00000361547.6:c.1282-79_1282-78del	ENSP00000355141.2:n.1282-79_1282-78del
ENST00000374315.1:c.1180-79_1180-78del	ENSP00000363434.1:n.1180-79_1180-78del
ENST00000559265.1:n.255+729_255+730del
NM_020451.2:c.1282-79_1282-78del	NP_065184.2:n.1282-79_1282-78del
NM_206926.1:c.1180-79_1180-78del	NP_996809.1:n.1180-79_1180-78del
NM_020451.3:c.1282-79_1282-78del MANE Select	NP_065184.2:n.1282-79_1282-78del
NM_206926.2:c.1180-79_1180-78del	NP_996809.1:n.1180-79_1180-78del