Canonical Allele Identifier: CA999780477

Gene: SELENON

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25800243_25800252del , CM000663.2:g.25800243_25800252del	GRCh38
NC_000001.10:g.26126734_26126743del , CM000663.1:g.26126734_26126743del	GRCh37
NC_000001.9:g.25999321_25999330del	NCBI36
NG_009930.1:g.5068_5077del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354177.9:c.13_22del	ENSP00000346109.5:p.Arg5AsnfsTer?
ENST00000494537.2:c.13_22del	ENSP00000508308.1:p.Arg5AsnfsTer?
ENST00000361547.7:c.13_22del MANE Select	ENSP00000355141.2:p.Arg5AsnfsTer?
ENST00000354177.8:c.13_22del	ENSP00000346109.4:p.Arg5AsnfsTer?
ENST00000361547.6:c.13_22del	ENSP00000355141.2:p.Arg5AsnfsTer?
ENST00000374315.1:c.13_22del	ENSP00000363434.1:p.Arg5AsnfsTer?
NM_020451.2:c.13_22del	NP_065184.2:p.Arg5AsnfsTer?
NM_206926.1:c.13_22del	NP_996809.1:p.Arg5AsnfsTer?
NM_020451.3:c.13_22del MANE Select	NP_065184.2:p.Arg5AsnfsTer?
NM_206926.2:c.13_22del	NP_996809.1:p.Arg5AsnfsTer?