Canonical Allele Identifier: CA1159806107

Gene: SELENON

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25808972G= , CM000663.2:g.25808972G=	GRCh38
NC_000001.10:g.26135463G= , CM000663.1:g.26135463G=	GRCh37
NC_000001.9:g.26008050G=	NCBI36
NG_009930.1:g.13797G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354177.9:c.646-123G=	ENSP00000346109.5:n.646-123G=
ENST00000494537.2:c.646-54G=	ENSP00000508308.1:n.646-54G=
ENST00000361547.7:c.748-54G= MANE Select	ENSP00000355141.2:n.748-54G=
ENST00000354177.8:c.646-54G=	ENSP00000346109.4:n.646-54G=
ENST00000361547.6:c.748-54G=	ENSP00000355141.2:n.748-54G=
ENST00000374315.1:c.646-54G=	ENSP00000363434.1:n.646-54G=
NM_020451.2:c.748-54G=	NP_065184.2:n.748-54G=
NM_206926.1:c.646-54G=	NP_996809.1:n.646-54G=
NM_020451.3:c.748-54G= MANE Select	NP_065184.2:n.748-54G=
NM_206926.2:c.646-54G=	NP_996809.1:n.646-54G=