Canonical Allele Identifier: CA339117695

Gene: SELENON

Linked Data

• MyVariant Identifiers: chr1:g.26139191C>G (hg19) ; chr1:g.25812700C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25812700C>G , CM000663.2:g.25812700C>G	GRCh38
NC_000001.10:g.26139191C>G , CM000663.1:g.26139191C>G	GRCh37
NC_000001.9:g.26011778C>G	NCBI36
NG_009930.1:g.17525C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354177.9:c.1124C>G	ENSP00000346109.5:p.Pro375Arg
ENST00000494537.2:c.1193C>G	ENSP00000508308.1:p.Pro398Arg
ENST00000361547.7:c.1295C>G MANE Select	ENSP00000355141.2:p.Pro432Arg
ENST00000354177.8:c.1193C>G	ENSP00000346109.4:p.Pro398Arg
ENST00000361547.6:c.1295C>G	ENSP00000355141.2:p.Pro432Arg
ENST00000374315.1:c.1193C>G	ENSP00000363434.1:p.Pro398Arg
ENST00000559265.1:n.255+821C>G
ENST00000630065.2:c.-278C>G	ENSP00000487549.1:n.-278C>G
NM_020451.2:c.1295C>G	NP_065184.2:p.Pro432Arg
NM_206926.1:c.1193C>G	NP_996809.1:p.Pro398Arg
NM_020451.3:c.1295C>G MANE Select	NP_065184.2:p.Pro432Arg
NM_206926.2:c.1193C>G	NP_996809.1:p.Pro398Arg