Canonical Allele Identifier: CA2574271268
Gene: SELENON HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.25809007T>A , CM000663.2:g.25809007T>A GRCh38
NC_000001.10:g.26135498T>A , CM000663.1:g.26135498T>A GRCh37
NC_000001.9:g.26008085T>A NCBI36
NG_009930.1:g.13832T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000354177.9:c.646-88T>A ENSP00000346109.5:n.646-88T>A
ENST00000494537.2:c.646-19T>A ENSP00000508308.1:n.646-19T>A
ENST00000361547.7:c.748-19T>A MANE Select ENSP00000355141.2:n.748-19T>A
ENST00000354177.8:c.646-19T>A ENSP00000346109.4:n.646-19T>A
ENST00000361547.6:c.748-19T>A ENSP00000355141.2:n.748-19T>A
ENST00000374315.1:c.646-19T>A ENSP00000363434.1:n.646-19T>A
NM_020451.2:c.748-19T>A NP_065184.2:n.748-19T>A
NM_206926.1:c.646-19T>A NP_996809.1:n.646-19T>A
NM_020451.3:c.748-19T>A MANE Select NP_065184.2:n.748-19T>A
NM_206926.2:c.646-19T>A NP_996809.1:n.646-19T>A
Search 100 bp 5'
Search 100 bp 3'