Canonical Allele Identifier: CA696923

Gene: SELENON

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25814150T>G , CM000663.2:g.25814150T>G	GRCh38
NC_000001.10:g.26140641T>G , CM000663.1:g.26140641T>G	GRCh37
NC_000001.9:g.26013228T>G	NCBI36
NG_009930.1:g.18975T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_020451.3:c.1574T>G MANE Select	NP_065184.2:p.Met525Arg
ENST00000361547.7:c.1574T>G MANE Select	ENSP00000355141.2:p.Met525Arg
NM_020451.2:c.1574T>G	NP_065184.2:p.Met525Arg
NM_206926.1:c.1472T>G	NP_996809.1:p.Met491Arg
NM_206926.2:c.1472T>G	NP_996809.1:p.Met491Arg
ENST00000354177.8:c.1472T>G	ENSP00000346109.4:p.Met491Arg
ENST00000354177.9:c.1403T>G	ENSP00000346109.5:p.Met468Arg
ENST00000361547.6:c.1574T>G	ENSP00000355141.2:p.Met525Arg
ENST00000374315.1:c.1472T>G	ENSP00000363434.1:p.Met491Arg
ENST00000494537.1:n.341T>G
ENST00000494537.2:c.1561T>G	ENSP00000508308.1:n.1561T>G
ENST00000527604.1:c.95T>G	ENSP00000457066.1:p.Met32Arg
ENST00000559265.1:n.255+2271T>G
ENST00000630065.2:c.2T>G	ENSP00000487549.1:p.Met1Arg