Canonical Allele Identifier: CA372650644

Gene: TONSL MIR6893 TONSL-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144435552T>C , CM000670.2:g.144435552T>C	GRCh38
NC_000008.10:g.145660935T>C , CM000670.1:g.145660935T>C	GRCh37
NC_000008.9:g.145631743T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_013432.5:c.2776-2A>G (TONSL) MANE Select	NP_038460.4:n.2776-2A>G
ENST00000409379.8:c.2776-2A>G (TONSL) MANE Select	ENSP00000386239.3:n.2776-2A>G
NM_013432.4:c.2776-2A>G (TONSL)	NP_038460.4:n.2776-2A>G
NR_106953.1:n.68A>G (MIR6893)
NR_109770.1:n.273+112T>C (TONSL-AS1)
ENST00000409379.7:c.2776-2A>G (TONSL)	ENSP00000386239.3:n.2776-2A>G
ENST00000497613.2:n.3751-2A>G (TONSL)
XM_011517047.1:c.2776-2A>G (TONSL)	XP_011515349.1:n.2776-2A>G
XM_011517048.1:c.1804-2A>G (TONSL)	XP_011515350.1:n.1804-2A>G
XM_011517048.2:c.1804-2A>G (TONSL)	XP_011515350.1:n.1804-2A>G
XM_011517049.1:c.1768-2A>G (TONSL)	XP_011515351.1:n.1768-2A>G
XM_011517049.2:c.1768-2A>G (TONSL)	XP_011515351.1:n.1768-2A>G
XM_011517050.1:c.2780-2A>G (TONSL)	XP_011515352.1:n.2780-2A>G
XM_011517050.2:c.2780-2A>G (TONSL)	XP_011515352.1:n.2780-2A>G