Canonical Allele Identifier: CA16042386
Gene: SELENON HGNC NCBI

Linked Data

ClinVar Variation Id: 372502
ClinVar RCV Id: RCV000413433
dbSNP Id: rs1057517819
MyVariant Identifiers: chr1:g.26139255G>C (hg19) chr1:g.25812764G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.25812764G>C , CM000663.2:g.25812764G>C GRCh38
NC_000001.10:g.26139255G>C , CM000663.1:g.26139255G>C GRCh37
NC_000001.9:g.26011842G>C NCBI36
NG_009930.1:g.17589G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000354177.9:c.1188G>C ENSP00000346109.5:p.Trp396Cys
ENST00000494537.2:c.1257G>C ENSP00000508308.1:p.Trp419Cys
ENST00000361547.7:c.1359G>C MANE Select ENSP00000355141.2:p.Trp453Cys
ENST00000354177.8:c.1257G>C ENSP00000346109.4:p.Trp419Cys
ENST00000361547.6:c.1359G>C ENSP00000355141.2:p.Trp453Cys
ENST00000374315.1:c.1257G>C ENSP00000363434.1:p.Trp419Cys
ENST00000494537.1:n.37G>C
ENST00000559265.1:n.255+885G>C
ENST00000630065.2:c.-214G>C ENSP00000487549.1:n.-214G>C
NM_020451.2:c.1359G>C NP_065184.2:p.Trp453Cys
NM_206926.1:c.1257G>C NP_996809.1:p.Trp419Cys
NM_020451.3:c.1359G>C MANE Select NP_065184.2:p.Trp453Cys
NM_206926.2:c.1257G>C NP_996809.1:p.Trp419Cys
Search 100 bp 5'
Search 100 bp 3'