Canonical Allele Identifier: CA339117846

Gene: SELENON

Linked Data

• MyVariant Identifiers: chr1:g.26139266A>C (hg19) ; chr1:g.25812775A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25812775A>C , CM000663.2:g.25812775A>C	GRCh38
NC_000001.10:g.26139266A>C , CM000663.1:g.26139266A>C	GRCh37
NC_000001.9:g.26011853A>C	NCBI36
NG_009930.1:g.17600A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354177.9:c.1199A>C	ENSP00000346109.5:p.Asp400Ala
ENST00000494537.2:c.1268A>C	ENSP00000508308.1:p.Asp423Ala
ENST00000361547.7:c.1370A>C MANE Select	ENSP00000355141.2:p.Asp457Ala
ENST00000354177.8:c.1268A>C	ENSP00000346109.4:p.Asp423Ala
ENST00000361547.6:c.1370A>C	ENSP00000355141.2:p.Asp457Ala
ENST00000374315.1:c.1268A>C	ENSP00000363434.1:p.Asp423Ala
ENST00000494537.1:n.48A>C
ENST00000559265.1:n.255+896A>C
ENST00000630065.2:c.-203A>C	ENSP00000487549.1:n.-203A>C
NM_020451.2:c.1370A>C	NP_065184.2:p.Asp457Ala
NM_206926.1:c.1268A>C	NP_996809.1:p.Asp423Ala
NM_020451.3:c.1370A>C MANE Select	NP_065184.2:p.Asp457Ala
NM_206926.2:c.1268A>C	NP_996809.1:p.Asp423Ala