Canonical Allele Identifier: CA223588
Community Standard Title: NM_020451.3(SELENON):c.301+1G>T
Gene: SELENON HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.25801161G>T , CM000663.2:g.25801161G>T GRCh38
NC_000001.10:g.26127652G>T , CM000663.1:g.26127652G>T GRCh37
NC_000001.9:g.26000239G>T NCBI36
NG_009930.1:g.5986G>T

Transcript Alleles

HGVS Amino-acid Change
NM_020451.3:c.301+1G>T MANE Select NP_065184.2:n.301+1G>T
ENST00000361547.7:c.301+1G>T MANE Select ENSP00000355141.2:n.301+1G>T
NM_020451.2:c.301+1G>T NP_065184.2:n.301+1G>T
NM_206926.1:c.301+1G>T NP_996809.1:n.301+1G>T
NM_206926.2:c.301+1G>T NP_996809.1:n.301+1G>T
ENST00000354177.8:c.301+1G>T ENSP00000346109.4:n.301+1G>T
ENST00000354177.9:c.301+1G>T ENSP00000346109.5:n.301+1G>T
ENST00000361547.6:c.301+1G>T ENSP00000355141.2:n.301+1G>T
ENST00000374315.1:c.301+1G>T ENSP00000363434.1:n.301+1G>T
ENST00000494537.2:c.301+1G>T ENSP00000508308.1:n.301+1G>T