Canonical Allele Identifier: CA187667106
Community Standard Title: NM_013432.5(TONSL):c.2623C>T (p.Arg875Ter)
Gene: TONSL HGNC NCBI
TONSL-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.144435810G>A , CM000670.2:g.144435810G>A GRCh38
NC_000008.10:g.145661193G>A , CM000670.1:g.145661193G>A GRCh37
NC_000008.9:g.145632001G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_013432.5:c.2623C>T (TONSL) MANE Select NP_038460.4:p.Arg875Ter
ENST00000409379.8:c.2623C>T (TONSL) MANE Select ENSP00000386239.3:p.Arg875Ter
NM_013432.4:c.2623C>T (TONSL) NP_038460.4:p.Arg875Ter
NR_109770.1:n.273+370G>A (TONSL-AS1)
ENST00000409379.7:c.2623C>T (TONSL) ENSP00000386239.3:p.Arg875Ter
ENST00000497613.2:n.3598C>T (TONSL)
XM_011517047.1:c.2623C>T (TONSL) XP_011515349.1:p.Arg875Ter
XM_011517048.1:c.1651C>T (TONSL) XP_011515350.1:p.Arg551Ter
XM_011517048.2:c.1651C>T (TONSL) XP_011515350.1:p.Arg551Ter
XM_011517049.1:c.1615C>T (TONSL) XP_011515351.1:p.Arg539Ter
XM_011517049.2:c.1615C>T (TONSL) XP_011515351.1:p.Arg539Ter
XM_011517050.1:c.2623C>T (TONSL) XP_011515352.1:p.Arg875Ter
XM_011517050.2:c.2623C>T (TONSL) XP_011515352.1:p.Arg875Ter