Canonical Allele Identifier: CA1143328089

Gene: SELENON

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25809014C= , CM000663.2:g.25809014C=	GRCh38
NC_000001.10:g.26135505C= , CM000663.1:g.26135505C=	GRCh37
NC_000001.9:g.26008092C=	NCBI36
NG_009930.1:g.13839C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000354177.9:c.646-81C=	ENSP00000346109.5:n.646-81C=
ENST00000494537.2:c.646-12C=	ENSP00000508308.1:n.646-12C=
ENST00000361547.7:c.748-12C= MANE Select	ENSP00000355141.2:n.748-12C=
ENST00000354177.8:c.646-12C=	ENSP00000346109.4:n.646-12C=
ENST00000361547.6:c.748-12C=	ENSP00000355141.2:n.748-12C=
ENST00000374315.1:c.646-12C=	ENSP00000363434.1:n.646-12C=
NM_020451.2:c.748-12C=	NP_065184.2:n.748-12C=
NM_206926.1:c.646-12C=	NP_996809.1:n.646-12C=
NM_020451.3:c.748-12C= MANE Select	NP_065184.2:n.748-12C=
NM_206926.2:c.646-12C=	NP_996809.1:n.646-12C=