Canonical Allele Identifier: CA696609

Gene: SELENON

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25808774G>A , CM000663.2:g.25808774G>A	GRCh38
NC_000001.10:g.26135265G>A , CM000663.1:g.26135265G>A	GRCh37
NC_000001.9:g.26007852G>A	NCBI36
NG_009930.1:g.13599G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354177.9:c.630G>A	ENSP00000346109.5:p.Pro210=
ENST00000494537.2:c.630G>A	ENSP00000508308.1:p.Pro210=
ENST00000361547.7:c.732G>A MANE Select	ENSP00000355141.2:p.Pro244=
ENST00000354177.8:c.630G>A	ENSP00000346109.4:p.Pro210=
ENST00000361547.6:c.732G>A	ENSP00000355141.2:p.Pro244=
ENST00000374315.1:c.630G>A	ENSP00000363434.1:p.Pro210=
NM_020451.2:c.732G>A	NP_065184.2:p.Pro244=
NM_206926.1:c.630G>A	NP_996809.1:p.Pro210=
NM_020451.3:c.732G>A MANE Select	NP_065184.2:p.Pro244=
NM_206926.2:c.630G>A	NP_996809.1:p.Pro210=