Canonical Allele Identifier: CA696650

Gene: SELENON

Linked Data

• dbSNP Id: rs537777571
• ExAC: 1:26135591 T / C
• gnomAD v2: 1-26135591-T-C
• gnomAD v3: 1-25809100-T-C
• gnomAD v4: 1-25809100-T-C
• MyVariant Identifiers: chr1:g.26135591T>C (hg19) ; chr1:g.25809100T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25809100T>C , CM000663.2:g.25809100T>C	GRCh38
NC_000001.10:g.26135591T>C , CM000663.1:g.26135591T>C	GRCh37
NC_000001.9:g.26008178T>C	NCBI36
NG_009930.1:g.13925T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000354177.9:c.651T>C	ENSP00000346109.5:p.Ala217=
ENST00000494537.2:c.720T>C	ENSP00000508308.1:p.Ala240=
ENST00000361547.7:c.822T>C MANE Select	ENSP00000355141.2:p.Ala274=
ENST00000354177.8:c.720T>C	ENSP00000346109.4:p.Ala240=
ENST00000361547.6:c.822T>C	ENSP00000355141.2:p.Ala274=
ENST00000374315.1:c.720T>C	ENSP00000363434.1:p.Ala240=
NM_020451.2:c.822T>C	NP_065184.2:p.Ala274=
NM_206926.1:c.720T>C	NP_996809.1:p.Ala240=
NM_020451.3:c.822T>C MANE Select	NP_065184.2:p.Ala274=
NM_206926.2:c.720T>C	NP_996809.1:p.Ala240=