Canonical Allele Identifier: CA339117843

Gene: SELENON

Linked Data

• MyVariant Identifiers: chr1:g.26139265G>A (hg19) ; chr1:g.25812774G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25812774G>A , CM000663.2:g.25812774G>A	GRCh38
NC_000001.10:g.26139265G>A , CM000663.1:g.26139265G>A	GRCh37
NC_000001.9:g.26011852G>A	NCBI36
NG_009930.1:g.17599G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000354177.9:c.1198G>A	ENSP00000346109.5:p.Asp400Asn
ENST00000494537.2:c.1267G>A	ENSP00000508308.1:p.Asp423Asn
ENST00000361547.7:c.1369G>A MANE Select	ENSP00000355141.2:p.Asp457Asn
ENST00000354177.8:c.1267G>A	ENSP00000346109.4:p.Asp423Asn
ENST00000361547.6:c.1369G>A	ENSP00000355141.2:p.Asp457Asn
ENST00000374315.1:c.1267G>A	ENSP00000363434.1:p.Asp423Asn
ENST00000494537.1:n.47G>A
ENST00000559265.1:n.255+895G>A
ENST00000630065.2:c.-204G>A	ENSP00000487549.1:n.-204G>A
NM_020451.2:c.1369G>A	NP_065184.2:p.Asp457Asn
NM_206926.1:c.1267G>A	NP_996809.1:p.Asp423Asn
NM_020451.3:c.1369G>A MANE Select	NP_065184.2:p.Asp457Asn
NM_206926.2:c.1267G>A	NP_996809.1:p.Asp423Asn