Canonical Allele Identifier: CA339113894
Gene: SELENON HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.25809096G>C , CM000663.2:g.25809096G>C GRCh38
NC_000001.10:g.26135587G>C , CM000663.1:g.26135587G>C GRCh37
NC_000001.9:g.26008174G>C NCBI36
NG_009930.1:g.13921G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000354177.9:c.647G>C ENSP00000346109.5:p.Gly216Ala
ENST00000494537.2:c.716G>C ENSP00000508308.1:p.Gly239Ala
ENST00000361547.7:c.818G>C MANE Select ENSP00000355141.2:p.Gly273Ala
ENST00000354177.8:c.716G>C ENSP00000346109.4:p.Gly239Ala
ENST00000361547.6:c.818G>C ENSP00000355141.2:p.Gly273Ala
ENST00000374315.1:c.716G>C ENSP00000363434.1:p.Gly239Ala
NM_020451.2:c.818G>C NP_065184.2:p.Gly273Ala
NM_206926.1:c.716G>C NP_996809.1:p.Gly239Ala
NM_020451.3:c.818G>C MANE Select NP_065184.2:p.Gly273Ala
NM_206926.2:c.716G>C NP_996809.1:p.Gly239Ala