Canonical Allele Identifier: CA696479

Gene: SELENON

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25802116G>A , CM000663.2:g.25802116G>A	GRCh38
NC_000001.10:g.26128607G>A , CM000663.1:g.26128607G>A	GRCh37
NC_000001.9:g.26001194G>A	NCBI36
NG_009930.1:g.6941G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_020451.3:c.402G>A MANE Select	NP_065184.2:p.Leu134=
ENST00000361547.7:c.402G>A MANE Select	ENSP00000355141.2:p.Leu134=
NM_020451.2:c.402G>A	NP_065184.2:p.Leu134=
NM_206926.1:c.301+956G>A	NP_996809.1:n.301+956G>A
NM_206926.2:c.301+956G>A	NP_996809.1:n.301+956G>A
ENST00000354177.8:c.301+956G>A	ENSP00000346109.4:n.301+956G>A
ENST00000354177.9:c.301+956G>A	ENSP00000346109.5:n.301+956G>A
ENST00000361547.6:c.402G>A	ENSP00000355141.2:p.Leu134=
ENST00000374315.1:c.301+956G>A	ENSP00000363434.1:n.301+956G>A
ENST00000494537.2:c.301+956G>A	ENSP00000508308.1:n.301+956G>A