Canonical Allele Identifier: CA19698407
Gene: SELENON HGNC NCBI

Linked Data

dbSNP Id: rs964354801
gnomAD v4: 1-25809107-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.25809107T>G , CM000663.2:g.25809107T>G GRCh38
NC_000001.10:g.26135598T>G , CM000663.1:g.26135598T>G GRCh37
NC_000001.9:g.26008185T>G NCBI36
NG_009930.1:g.13932T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000354177.9:c.658T>G ENSP00000346109.5:p.Cys220Gly
ENST00000494537.2:c.727T>G ENSP00000508308.1:p.Cys243Gly
ENST00000361547.7:c.829T>G MANE Select ENSP00000355141.2:p.Cys277Gly
ENST00000354177.8:c.727T>G ENSP00000346109.4:p.Cys243Gly
ENST00000361547.6:c.829T>G ENSP00000355141.2:p.Cys277Gly
ENST00000374315.1:c.727T>G ENSP00000363434.1:p.Cys243Gly
NM_020451.2:c.829T>G NP_065184.2:p.Cys277Gly
NM_206926.1:c.727T>G NP_996809.1:p.Cys243Gly
NM_020451.3:c.829T>G MANE Select NP_065184.2:p.Cys277Gly
NM_206926.2:c.727T>G NP_996809.1:p.Cys243Gly