Canonical Allele Identifier: CA4942837

Gene: TONSL TONSL-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144436026G>A , CM000670.2:g.144436026G>A	GRCh38
NC_000008.10:g.145661409G>A , CM000670.1:g.145661409G>A	GRCh37
NC_000008.9:g.145632217G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_013432.5:c.2407C>T (TONSL) MANE Select	NP_038460.4:p.Gln803Ter
ENST00000409379.8:c.2407C>T (TONSL) MANE Select	ENSP00000386239.3:p.Gln803Ter
NM_013432.4:c.2407C>T (TONSL)	NP_038460.4:p.Gln803Ter
NR_109770.1:n.273+586G>A (TONSL-AS1)
ENST00000409379.7:c.2407C>T (TONSL)	ENSP00000386239.3:p.Gln803Ter
ENST00000497613.2:n.3382C>T (TONSL)
XM_011517047.1:c.2407C>T (TONSL)	XP_011515349.1:p.Gln803Ter
XM_011517048.1:c.1435C>T (TONSL)	XP_011515350.1:p.Gln479Ter
XM_011517048.2:c.1435C>T (TONSL)	XP_011515350.1:p.Gln479Ter
XM_011517049.1:c.1399C>T (TONSL)	XP_011515351.1:p.Gln467Ter
XM_011517049.2:c.1399C>T (TONSL)	XP_011515351.1:p.Gln467Ter
XM_011517050.1:c.2407C>T (TONSL)	XP_011515352.1:p.Gln803Ter
XM_011517050.2:c.2407C>T (TONSL)	XP_011515352.1:p.Gln803Ter