Canonical Allele Identifier: CA696566

Gene: SELENON

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25808607C>T , CM000663.2:g.25808607C>T	GRCh38
NC_000001.10:g.26135098C>T , CM000663.1:g.26135098C>T	GRCh37
NC_000001.9:g.26007685C>T	NCBI36
NG_009930.1:g.13432C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_020451.3:c.565C>T MANE Select	NP_065184.2:p.Arg189Ter
ENST00000361547.7:c.565C>T MANE Select	ENSP00000355141.2:p.Arg189Ter
NM_020451.2:c.565C>T	NP_065184.2:p.Arg189Ter
NM_206926.1:c.463C>T	NP_996809.1:p.Arg155Ter
NM_206926.2:c.463C>T	NP_996809.1:p.Arg155Ter
ENST00000354177.8:c.463C>T	ENSP00000346109.4:p.Arg155Ter
ENST00000354177.9:c.463C>T	ENSP00000346109.5:p.Arg155Ter
ENST00000361547.6:c.565C>T	ENSP00000355141.2:p.Arg189Ter
ENST00000374315.1:c.463C>T	ENSP00000363434.1:p.Arg155Ter
ENST00000494537.2:c.463C>T	ENSP00000508308.1:p.Arg155Ter