Canonical Allele Identifier: CA2228911860

Gene: TK2

Linked Data

• dbSNP Id: rs1965020217
• gnomAD v4: 16-66528958-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66528958G>T , CM000678.2:g.66528958G>T	GRCh38
NC_000016.9:g.66562861G>T , CM000678.1:g.66562861G>T	GRCh37
NC_000016.8:g.65120362G>T	NCBI36
NG_016862.1:g.26455C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299697.12:c.281+36C>A	ENSP00000299697.9:n.281+36C>A
ENST00000417693.8:c.395+36C>A	ENSP00000407469.5:n.395+36C>A
ENST00000451102.7:c.356+36C>A	ENSP00000414334.4:n.356+36C>A
ENST00000527284.6:c.393+36C>A
ENST00000527800.6:c.158+36C>A	ENSP00000433770.1:n.158+36C>A
ENST00000544898.6:c.449+36C>A MANE Select	ENSP00000440898.2:n.449+36C>A
ENST00000567357.6:c.*307+36C>A	ENSP00000457959.2:n.*307+36C>A
ENST00000569718.6:c.356+36C>A	ENSP00000464313.2:n.356+36C>A
ENST00000620035.5:c.374+36C>A	ENSP00000483833.2:n.374+36C>A
ENST00000676538.1:c.33-11081C>A
ENST00000677379.1:c.90+2422C>A	ENSP00000503672.1:n.90+2422C>A
ENST00000677420.1:c.158+36C>A	ENSP00000504648.1:n.158+36C>A
ENST00000677555.1:c.158+36C>A	ENSP00000503331.1:n.158+36C>A
ENST00000677715.1:c.158+36C>A	ENSP00000502950.1:n.158+36C>A
ENST00000678015.1:c.158+36C>A	ENSP00000502959.1:n.158+36C>A
ENST00000678297.1:c.158+36C>A	ENSP00000503472.1:n.158+36C>A
ENST00000678314.1:c.158+36C>A	ENSP00000504438.1:n.158+36C>A
ENST00000299697.11:c.449+36C>A	ENSP00000299697.8:n.449+36C>A
ENST00000417693.7:c.521+36C>A	ENSP00000407469.4:n.521+36C>A
ENST00000451102.6:c.575+36C>A	ENSP00000414334.3:n.575+36C>A
ENST00000525974.5:c.158+36C>A	ENSP00000434594.1:n.158+36C>A
ENST00000527284.5:c.356+36C>A	ENSP00000435312.1:n.356+36C>A
ENST00000527800.5:c.158+36C>A	ENSP00000433770.1:n.158+36C>A
ENST00000544898.5:c.449+36C>A	ENSP00000440898.2:n.449+36C>A
ENST00000545043.6:c.374+36C>A	ENSP00000438143.2:n.374+36C>A
ENST00000562484.2:c.158+36C>A	ENSP00000463326.1:n.158+36C>A
ENST00000563369.6:c.158+36C>A	ENSP00000463560.1:n.158+36C>A
ENST00000563478.5:c.158+36C>A	ENSP00000462341.1:n.158+36C>A
ENST00000564917.5:c.449+36C>A	ENSP00000455187.1:n.449+36C>A
ENST00000567357.5:c.*307+36C>A	ENSP00000457959.1:n.*307+36C>A
ENST00000569718.5:c.343+36C>A
ENST00000620035.4:c.395+36C>A	ENSP00000483833.1:n.395+36C>A
NM_001172643.1:c.356+36C>A	NP_001166114.1:n.356+36C>A
NM_001172644.1:c.374+36C>A	NP_001166115.1:n.374+36C>A
NM_001172645.1:c.395+36C>A	NP_001166116.1:n.395+36C>A
NM_001271934.1:c.302+36C>A	NP_001258863.1:n.302+36C>A
NM_001271935.1:c.356+36C>A	NP_001258864.1:n.356+36C>A
NM_001272050.1:c.158+36C>A	NP_001258979.1:n.158+36C>A
NM_004614.4:c.449+36C>A	NP_004605.4:n.449+36C>A
NR_073520.1:n.1728+36C>A
NM_001172644.2:c.374+36C>A	NP_001166115.1:n.374+36C>A
NM_001271934.2:c.302+36C>A	NP_001258863.1:n.302+36C>A
NM_001272050.2:c.158+36C>A	NP_001258979.1:n.158+36C>A
NM_004614.5:c.449+36C>A MANE Select	NP_004605.4:n.449+36C>A
NR_073520.2:n.1438+36C>A
NM_001172645.2:c.395+36C>A	NP_001166116.1:n.395+36C>A