Canonical Allele Identifier: CA696789

Gene: SELENON

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25811778G>T , CM000663.2:g.25811778G>T	GRCh38
NC_000001.10:g.26138269G>T , CM000663.1:g.26138269G>T	GRCh37
NC_000001.9:g.26010856G>T	NCBI36
NG_009930.1:g.16603G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_020451.3:c.1180G>T MANE Select	NP_065184.2:p.Glu394Ter
ENST00000361547.7:c.1180G>T MANE Select	ENSP00000355141.2:p.Glu394Ter
NM_020451.2:c.1180G>T	NP_065184.2:p.Glu394Ter
NM_206926.1:c.1078G>T	NP_996809.1:p.Glu360Ter
NM_206926.2:c.1078G>T	NP_996809.1:p.Glu360Ter
ENST00000354177.8:c.1078G>T	ENSP00000346109.4:p.Glu360Ter
ENST00000354177.9:c.1009G>T	ENSP00000346109.5:p.Glu337Ter
ENST00000361547.6:c.1180G>T	ENSP00000355141.2:p.Glu394Ter
ENST00000374315.1:c.1078G>T	ENSP00000363434.1:p.Glu360Ter
ENST00000494537.2:c.1078G>T	ENSP00000508308.1:p.Glu360Ter
ENST00000559265.1:n.154G>T