Canonical Allele Identifier: CA2832533882

Gene: SELENON

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25808962dup , CM000663.2:g.25808962dup	GRCh38
NC_000001.10:g.26135453dup , CM000663.1:g.26135453dup	GRCh37
NC_000001.9:g.26008040dup	NCBI36
NG_009930.1:g.13787dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354177.9:c.646-133dup	ENSP00000346109.5:n.646-133dup
ENST00000494537.2:c.646-64dup	ENSP00000508308.1:n.646-64dup
ENST00000361547.7:c.748-64dup MANE Select	ENSP00000355141.2:n.748-64dup
ENST00000354177.8:c.646-64dup	ENSP00000346109.4:n.646-64dup
ENST00000361547.6:c.748-64dup	ENSP00000355141.2:n.748-64dup
ENST00000374315.1:c.646-64dup	ENSP00000363434.1:n.646-64dup
NM_020451.2:c.748-64dup	NP_065184.2:n.748-64dup
NM_206926.1:c.646-64dup	NP_996809.1:n.646-64dup
NM_020451.3:c.748-64dup MANE Select	NP_065184.2:n.748-64dup
NM_206926.2:c.646-64dup	NP_996809.1:n.646-64dup