Canonical Allele Identifier: CA1140829908

Gene: SELENON

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25809365T= , CM000663.2:g.25809365T=	GRCh38
NC_000001.10:g.26135856T= , CM000663.1:g.26135856T=	GRCh37
NC_000001.9:g.26008443T=	NCBI36
NG_009930.1:g.14190T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354177.9:c.701+215T=	ENSP00000346109.5:n.701+215T=
ENST00000494537.2:c.770+215T=	ENSP00000508308.1:n.770+215T=
ENST00000361547.7:c.872+215T= MANE Select	ENSP00000355141.2:n.872+215T=
ENST00000354177.8:c.770+215T=	ENSP00000346109.4:n.770+215T=
ENST00000361547.6:c.872+215T=	ENSP00000355141.2:n.872+215T=
ENST00000374315.1:c.770+215T=	ENSP00000363434.1:n.770+215T=
NM_020451.2:c.872+215T=	NP_065184.2:n.872+215T=
NM_206926.1:c.770+215T=	NP_996809.1:n.770+215T=
NM_020451.3:c.872+215T= MANE Select	NP_065184.2:n.872+215T=
NM_206926.2:c.770+215T=	NP_996809.1:n.770+215T=