Canonical Allele Identifier: CA339113995

Gene: SELENON

Linked Data

• MyVariant Identifiers: chr1:g.26135600C>G (hg19) ; chr1:g.25809109C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25809109C>G , CM000663.2:g.25809109C>G	GRCh38
NC_000001.10:g.26135600C>G , CM000663.1:g.26135600C>G	GRCh37
NC_000001.9:g.26008187C>G	NCBI36
NG_009930.1:g.13934C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000354177.9:c.660C>G	ENSP00000346109.5:p.Cys220Trp
ENST00000494537.2:c.729C>G	ENSP00000508308.1:p.Cys243Trp
ENST00000361547.7:c.831C>G MANE Select	ENSP00000355141.2:p.Cys277Trp
ENST00000354177.8:c.729C>G	ENSP00000346109.4:p.Cys243Trp
ENST00000361547.6:c.831C>G	ENSP00000355141.2:p.Cys277Trp
ENST00000374315.1:c.729C>G	ENSP00000363434.1:p.Cys243Trp
NM_020451.2:c.831C>G	NP_065184.2:p.Cys277Trp
NM_206926.1:c.729C>G	NP_996809.1:p.Cys243Trp
NM_020451.3:c.831C>G MANE Select	NP_065184.2:p.Cys277Trp
NM_206926.2:c.729C>G	NP_996809.1:p.Cys243Trp