Canonical Allele Identifier: CA339112027

Gene: SELENON

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25808707G>A , CM000663.2:g.25808707G>A	GRCh38
NC_000001.10:g.26135198G>A , CM000663.1:g.26135198G>A	GRCh37
NC_000001.9:g.26007785G>A	NCBI36
NG_009930.1:g.13532G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354177.9:c.563G>A	ENSP00000346109.5:p.Trp188Ter
ENST00000494537.2:c.563G>A	ENSP00000508308.1:p.Trp188Ter
ENST00000361547.7:c.665G>A MANE Select	ENSP00000355141.2:p.Trp222Ter
ENST00000354177.8:c.563G>A	ENSP00000346109.4:p.Trp188Ter
ENST00000361547.6:c.665G>A	ENSP00000355141.2:p.Trp222Ter
ENST00000374315.1:c.563G>A	ENSP00000363434.1:p.Trp188Ter
NM_020451.2:c.665G>A	NP_065184.2:p.Trp222Ter
NM_206926.1:c.563G>A	NP_996809.1:p.Trp188Ter
NM_020451.3:c.665G>A MANE Select	NP_065184.2:p.Trp222Ter
NM_206926.2:c.563G>A	NP_996809.1:p.Trp188Ter