Canonical Allele Identifier: CA696878

Gene: SELENON

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25813920C>T , CM000663.2:g.25813920C>T	GRCh38
NC_000001.10:g.26140411C>T , CM000663.1:g.26140411C>T	GRCh37
NC_000001.9:g.26012998C>T	NCBI36
NG_009930.1:g.18745C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354177.9:c.1256C>T	ENSP00000346109.5:p.Ser419Leu
ENST00000494537.2:c.1414C>T	ENSP00000508308.1:p.Arg472Cys
ENST00000361547.7:c.1427C>T MANE Select	ENSP00000355141.2:p.Ser476Leu
ENST00000354177.8:c.1325C>T	ENSP00000346109.4:p.Ser442Leu
ENST00000361547.6:c.1427C>T	ENSP00000355141.2:p.Ser476Leu
ENST00000374315.1:c.1325C>T	ENSP00000363434.1:p.Ser442Leu
ENST00000494537.1:n.194C>T
ENST00000559265.1:n.255+2041C>T
ENST00000630065.2:c.-146C>T	ENSP00000487549.1:n.-146C>T
NM_020451.2:c.1427C>T	NP_065184.2:p.Ser476Leu
NM_206926.1:c.1325C>T	NP_996809.1:p.Ser442Leu
NM_020451.3:c.1427C>T MANE Select	NP_065184.2:p.Ser476Leu
NM_206926.2:c.1325C>T	NP_996809.1:p.Ser442Leu