Canonical Allele Identifier: CA339117674

Gene: SELENON

Linked Data

• MyVariant Identifiers: chr1:g.26139182C>A (hg19) ; chr1:g.25812691C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25812691C>A , CM000663.2:g.25812691C>A	GRCh38
NC_000001.10:g.26139182C>A , CM000663.1:g.26139182C>A	GRCh37
NC_000001.9:g.26011769C>A	NCBI36
NG_009930.1:g.17516C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354177.9:c.1115C>A	ENSP00000346109.5:p.Ser372Tyr
ENST00000494537.2:c.1184C>A	ENSP00000508308.1:p.Ser395Tyr
ENST00000361547.7:c.1286C>A MANE Select	ENSP00000355141.2:p.Ser429Tyr
ENST00000354177.8:c.1184C>A	ENSP00000346109.4:p.Ser395Tyr
ENST00000361547.6:c.1286C>A	ENSP00000355141.2:p.Ser429Tyr
ENST00000374315.1:c.1184C>A	ENSP00000363434.1:p.Ser395Tyr
ENST00000559265.1:n.255+812C>A
ENST00000630065.2:c.-287C>A	ENSP00000487549.1:n.-287C>A
NM_020451.2:c.1286C>A	NP_065184.2:p.Ser429Tyr
NM_206926.1:c.1184C>A	NP_996809.1:p.Ser395Tyr
NM_020451.3:c.1286C>A MANE Select	NP_065184.2:p.Ser429Tyr
NM_206926.2:c.1184C>A	NP_996809.1:p.Ser395Tyr