Canonical Allele Identifier: CA495902960

Gene: TK2

Linked Data

• MyVariant Identifiers: chr16:g.66547664G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66513761G>T , CM000678.2:g.66513761G>T	GRCh38
NC_000016.9:g.66547664G>T , CM000678.1:g.66547664G>T	GRCh37
NC_000016.8:g.65105165G>T	NCBI36
NG_016862.1:g.41652C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299697.12:c.501C>A	ENSP00000299697.9:p.Gly167=
ENST00000417693.8:c.615C>A	ENSP00000407469.5:p.Gly205=
ENST00000451102.7:c.576C>A	ENSP00000414334.4:p.Gly192=
ENST00000527284.6:c.563-1695C>A
ENST00000527800.6:c.378C>A	ENSP00000433770.1:p.Gly126=
ENST00000544898.6:c.669C>A MANE Select	ENSP00000440898.2:p.Gly223=
ENST00000567357.6:c.*527C>A	ENSP00000457959.2:n.*527C>A
ENST00000569718.6:c.407C>A	ENSP00000464313.2:p.Ala136Glu
ENST00000620035.5:c.425C>A	ENSP00000483833.2:p.Ala142Glu
ENST00000676538.1:c.252C>A
ENST00000676904.1:c.140C>A
ENST00000677296.1:n.51C>A
ENST00000677379.1:c.310C>A	ENSP00000503672.1:n.310C>A
ENST00000677420.1:c.378C>A	ENSP00000504648.1:p.Gly126=
ENST00000677555.1:c.378C>A	ENSP00000503331.1:p.Gly126=
ENST00000677715.1:c.378C>A	ENSP00000502950.1:p.Gly126=
ENST00000677753.1:n.51C>A
ENST00000677961.1:n.81C>A
ENST00000678015.1:c.378C>A	ENSP00000502959.1:p.Gly126=
ENST00000678190.1:c.51C>A	ENSP00000503824.1:p.Gly17=
ENST00000678282.1:n.51C>A
ENST00000678297.1:c.378C>A	ENSP00000503472.1:p.Gly126=
ENST00000299697.11:c.669C>A	ENSP00000299697.8:p.Gly223=
ENST00000417693.7:c.741C>A	ENSP00000407469.4:p.Gly247=
ENST00000451102.6:c.795C>A	ENSP00000414334.3:p.Gly265=
ENST00000525974.5:c.378C>A	ENSP00000434594.1:p.Gly126=
ENST00000527284.5:c.576C>A	ENSP00000435312.1:p.Gly192=
ENST00000527800.5:c.378C>A	ENSP00000433770.1:p.Gly126=
ENST00000544898.5:c.669C>A	ENSP00000440898.2:p.Gly223=
ENST00000545043.6:c.594C>A	ENSP00000438143.2:p.Gly198=
ENST00000561527.5:n.228C>A
ENST00000561728.1:c.118C>A
ENST00000561905.2:c.23C>A
ENST00000562552.5:n.485C>A
ENST00000563099.5:n.196C>A
ENST00000563369.6:c.378C>A	ENSP00000463560.1:p.Gly126=
ENST00000563478.5:c.378C>A	ENSP00000462341.1:p.Gly126=
ENST00000564792.1:n.324C>A
ENST00000564917.5:c.720C>A	ENSP00000455187.1:p.Gly240=
ENST00000567357.5:c.*527C>A	ENSP00000457959.1:n.*527C>A
ENST00000569718.5:c.394C>A
ENST00000620035.4:c.615C>A	ENSP00000483833.1:p.Gly205=
NM_001172643.1:c.576C>A	NP_001166114.1:p.Gly192=
NM_001172644.1:c.594C>A	NP_001166115.1:p.Gly198=
NM_001172645.1:c.615C>A	NP_001166116.1:p.Gly205=
NM_001271934.1:c.522C>A	NP_001258863.1:p.Gly174=
NM_001271935.1:c.407C>A	NP_001258864.1:p.Ala136Glu
NM_001272050.1:c.378C>A	NP_001258979.1:p.Gly126=
NM_004614.4:c.669C>A	NP_004605.4:p.Gly223=
NR_073520.1:n.1948C>A
NM_001172644.2:c.594C>A	NP_001166115.1:p.Gly198=
NM_001271934.2:c.522C>A	NP_001258863.1:p.Gly174=
NM_001272050.2:c.378C>A	NP_001258979.1:p.Gly126=
NM_004614.5:c.669C>A MANE Select	NP_004605.4:p.Gly223=
NR_073520.2:n.1658C>A
NM_001172645.2:c.615C>A	NP_001166116.1:p.Gly205=