Canonical Allele Identifier: CA2523639901

Gene: SELENON

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25809368_25809369del , CM000663.2:g.25809368_25809369del	GRCh38
NC_000001.10:g.26135859_26135860del , CM000663.1:g.26135859_26135860del	GRCh37
NC_000001.9:g.26008446_26008447del	NCBI36
NG_009930.1:g.14193_14194del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354177.9:c.701+218_701+219del	ENSP00000346109.5:n.701+218_701+219del
ENST00000494537.2:c.770+218_770+219del	ENSP00000508308.1:n.770+218_770+219del
ENST00000361547.7:c.872+218_872+219del MANE Select	ENSP00000355141.2:n.872+218_872+219del
ENST00000354177.8:c.770+218_770+219del	ENSP00000346109.4:n.770+218_770+219del
ENST00000361547.6:c.872+218_872+219del	ENSP00000355141.2:n.872+218_872+219del
ENST00000374315.1:c.770+218_770+219del	ENSP00000363434.1:n.770+218_770+219del
NM_020451.2:c.872+218_872+219del	NP_065184.2:n.872+218_872+219del
NM_206926.1:c.770+218_770+219del	NP_996809.1:n.770+218_770+219del
NM_020451.3:c.872+218_872+219del MANE Select	NP_065184.2:n.872+218_872+219del
NM_206926.2:c.770+218_770+219del	NP_996809.1:n.770+218_770+219del