Canonical Allele Identifier: CA2228896374

Gene: TK2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66513807T= , CM000678.2:g.66513807T=	GRCh38
NC_000016.9:g.66547710T= , CM000678.1:g.66547710T=	GRCh37
NC_000016.8:g.65105211T=	NCBI36
NG_016862.1:g.41606A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299697.12:c.455A=	ENSP00000299697.9:p.Tyr152=
ENST00000417693.8:c.569A=	ENSP00000407469.5:p.Tyr190=
ENST00000451102.7:c.530A=	ENSP00000414334.4:p.Tyr177=
ENST00000527284.6:c.563-1741A=
ENST00000527800.6:c.332A=	ENSP00000433770.1:p.Tyr111=
ENST00000544898.6:c.623A= MANE Select	ENSP00000440898.2:p.Tyr208=
ENST00000567357.6:c.*481A=	ENSP00000457959.2:n.*481A=
ENST00000569718.6:c.361A=	ENSP00000464313.2:p.Thr121=
ENST00000620035.5:c.379A=	ENSP00000483833.2:p.Thr127=
ENST00000676538.1:c.206A=
ENST00000676904.1:c.94A=
ENST00000677296.1:n.5A=
ENST00000677379.1:c.264A=	ENSP00000503672.1:n.264A=
ENST00000677420.1:c.332A=	ENSP00000504648.1:p.Tyr111=
ENST00000677555.1:c.332A=	ENSP00000503331.1:p.Tyr111=
ENST00000677715.1:c.332A=	ENSP00000502950.1:p.Tyr111=
ENST00000677753.1:n.5A=
ENST00000677961.1:n.35A=
ENST00000678015.1:c.332A=	ENSP00000502959.1:p.Tyr111=
ENST00000678190.1:c.5A=	ENSP00000503824.1:p.Tyr2=
ENST00000678282.1:n.5A=
ENST00000678297.1:c.332A=	ENSP00000503472.1:p.Tyr111=
ENST00000299697.11:c.623A=	ENSP00000299697.8:p.Tyr208=
ENST00000417693.7:c.695A=	ENSP00000407469.4:p.Tyr232=
ENST00000451102.6:c.749A=	ENSP00000414334.3:p.Tyr250=
ENST00000525974.5:c.332A=	ENSP00000434594.1:p.Tyr111=
ENST00000527284.5:c.530A=	ENSP00000435312.1:p.Tyr177=
ENST00000527800.5:c.332A=	ENSP00000433770.1:p.Tyr111=
ENST00000544898.5:c.623A=	ENSP00000440898.2:p.Tyr208=
ENST00000545043.6:c.548A=	ENSP00000438143.2:p.Tyr183=
ENST00000561527.5:n.182A=
ENST00000561728.1:c.72A=
ENST00000562552.5:n.439A=
ENST00000563099.5:n.150A=
ENST00000563369.6:c.332A=	ENSP00000463560.1:p.Tyr111=
ENST00000563478.5:c.332A=	ENSP00000462341.1:p.Tyr111=
ENST00000564792.1:n.278A=
ENST00000564917.5:c.674A=	ENSP00000455187.1:p.Tyr225=
ENST00000567357.5:c.*481A=	ENSP00000457959.1:n.*481A=
ENST00000569718.5:c.348A=
ENST00000620035.4:c.569A=	ENSP00000483833.1:p.Tyr190=
NM_001172643.1:c.530A=	NP_001166114.1:p.Tyr177=
NM_001172644.1:c.548A=	NP_001166115.1:p.Tyr183=
NM_001172645.1:c.569A=	NP_001166116.1:p.Tyr190=
NM_001271934.1:c.476A=	NP_001258863.1:p.Tyr159=
NM_001271935.1:c.361A=	NP_001258864.1:p.Thr121=
NM_001272050.1:c.332A=	NP_001258979.1:p.Tyr111=
NM_004614.4:c.623A=	NP_004605.4:p.Tyr208=
NR_073520.1:n.1902A=
NM_001172644.2:c.548A=	NP_001166115.1:p.Tyr183=
NM_001271934.2:c.476A=	NP_001258863.1:p.Tyr159=
NM_001272050.2:c.332A=	NP_001258979.1:p.Tyr111=
NM_004614.5:c.623A= MANE Select	NP_004605.4:p.Tyr208=
NR_073520.2:n.1612A=
NM_001172645.2:c.569A=	NP_001166116.1:p.Tyr190=