Canonical Allele Identifier: CA339113976

Gene: SELENON

Linked Data

• MyVariant Identifiers: chr1:g.26135599G>T (hg19) ; chr1:g.25809108G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25809108G>T , CM000663.2:g.25809108G>T	GRCh38
NC_000001.10:g.26135599G>T , CM000663.1:g.26135599G>T	GRCh37
NC_000001.9:g.26008186G>T	NCBI36
NG_009930.1:g.13933G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000354177.9:c.659G>T	ENSP00000346109.5:p.Cys220Phe
ENST00000494537.2:c.728G>T	ENSP00000508308.1:p.Cys243Phe
ENST00000361547.7:c.830G>T MANE Select	ENSP00000355141.2:p.Cys277Phe
ENST00000354177.8:c.728G>T	ENSP00000346109.4:p.Cys243Phe
ENST00000361547.6:c.830G>T	ENSP00000355141.2:p.Cys277Phe
ENST00000374315.1:c.728G>T	ENSP00000363434.1:p.Cys243Phe
NM_020451.2:c.830G>T	NP_065184.2:p.Cys277Phe
NM_206926.1:c.728G>T	NP_996809.1:p.Cys243Phe
NM_020451.3:c.830G>T MANE Select	NP_065184.2:p.Cys277Phe
NM_206926.2:c.728G>T	NP_996809.1:p.Cys243Phe