Canonical Allele Identifier: CA339113709

Gene: SELENON

Linked Data

• MyVariant Identifiers: chr1:g.26135565A>T (hg19) ; chr1:g.25809074A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25809074A>T , CM000663.2:g.25809074A>T	GRCh38
NC_000001.10:g.26135565A>T , CM000663.1:g.26135565A>T	GRCh37
NC_000001.9:g.26008152A>T	NCBI36
NG_009930.1:g.13899A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354177.9:c.646-21A>T	ENSP00000346109.5:n.646-21A>T
ENST00000494537.2:c.694A>T	ENSP00000508308.1:p.Lys232Ter
ENST00000361547.7:c.796A>T MANE Select	ENSP00000355141.2:p.Lys266Ter
ENST00000354177.8:c.694A>T	ENSP00000346109.4:p.Lys232Ter
ENST00000361547.6:c.796A>T	ENSP00000355141.2:p.Lys266Ter
ENST00000374315.1:c.694A>T	ENSP00000363434.1:p.Lys232Ter
NM_020451.2:c.796A>T	NP_065184.2:p.Lys266Ter
NM_206926.1:c.694A>T	NP_996809.1:p.Lys232Ter
NM_020451.3:c.796A>T MANE Select	NP_065184.2:p.Lys266Ter
NM_206926.2:c.694A>T	NP_996809.1:p.Lys232Ter