Canonical Allele Identifier: CA416760007

Gene: SELENON

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25816825T>C , CM000663.2:g.25816825T>C	GRCh38
NC_000001.10:g.26143316T>C , CM000663.1:g.26143316T>C	GRCh37
NC_000001.9:g.26015903T>C	NCBI36
NG_009930.1:g.21650T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_020451.3:c.*1107T>C MANE Select	NP_065184.2:n.*1107T>C
ENST00000361547.7:c.*1107T>C MANE Select	ENSP00000355141.2:n.*1107T>C
NM_020451.2:c.*1107T>C	NP_065184.2:n.*1107T>C
NM_206926.1:c.*1107T>C	NP_996809.1:n.*1107T>C
NM_206926.2:c.*1107T>C	NP_996809.1:n.*1107T>C
ENST00000354177.8:c.*1107T>C	ENSP00000346109.4:n.*1107T>C
ENST00000361547.6:c.*1107T>C	ENSP00000355141.2:n.*1107T>C
ENST00000374315.1:c.*1107T>C	ENSP00000363434.1:n.*1107T>C
ENST00000527604.1:c.123+2647T>C	ENSP00000457066.1:n.123+2647T>C
ENST00000559265.1:n.255+4946T>C
ENST00000630065.2:c.*1107T>C	ENSP00000487549.1:n.*1107T>C