Canonical Allele Identifier: CA1159806270

Gene: SELENON

Linked Data

• dbSNP Id: rs2047938705

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25809431C>T , CM000663.2:g.25809431C>T	GRCh38
NC_000001.10:g.26135922C>T , CM000663.1:g.26135922C>T	GRCh37
NC_000001.9:g.26008509C>T	NCBI36
NG_009930.1:g.14256C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354177.9:c.702-252C>T	ENSP00000346109.5:n.702-252C>T
ENST00000494537.2:c.771-252C>T	ENSP00000508308.1:n.771-252C>T
ENST00000361547.7:c.873-252C>T MANE Select	ENSP00000355141.2:n.873-252C>T
ENST00000354177.8:c.771-252C>T	ENSP00000346109.4:n.771-252C>T
ENST00000361547.6:c.873-252C>T	ENSP00000355141.2:n.873-252C>T
ENST00000374315.1:c.771-252C>T	ENSP00000363434.1:n.771-252C>T
NM_020451.2:c.873-252C>T	NP_065184.2:n.873-252C>T
NM_206926.1:c.771-252C>T	NP_996809.1:n.771-252C>T
NM_020451.3:c.873-252C>T MANE Select	NP_065184.2:n.873-252C>T
NM_206926.2:c.771-252C>T	NP_996809.1:n.771-252C>T