Canonical Allele Identifier: CA495902983

Gene: TK2

Linked Data

• gnomAD v4: 16-66513782-A-G
• MyVariant Identifiers: chr16:g.66547685A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66513782A>G , CM000678.2:g.66513782A>G	GRCh38
NC_000016.9:g.66547685A>G , CM000678.1:g.66547685A>G	GRCh37
NC_000016.8:g.65105186A>G	NCBI36
NG_016862.1:g.41631T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299697.12:c.480T>C	ENSP00000299697.9:p.His160=
ENST00000417693.8:c.594T>C	ENSP00000407469.5:p.His198=
ENST00000451102.7:c.555T>C	ENSP00000414334.4:p.His185=
ENST00000527284.6:c.563-1716T>C
ENST00000527800.6:c.357T>C	ENSP00000433770.1:p.His119=
ENST00000544898.6:c.648T>C MANE Select	ENSP00000440898.2:p.His216=
ENST00000567357.6:c.*506T>C	ENSP00000457959.2:n.*506T>C
ENST00000569718.6:c.386T>C	ENSP00000464313.2:p.Met129Thr
ENST00000620035.5:c.404T>C	ENSP00000483833.2:p.Met135Thr
ENST00000676538.1:c.231T>C
ENST00000676904.1:c.119T>C
ENST00000677296.1:n.30T>C
ENST00000677379.1:c.289T>C	ENSP00000503672.1:n.289T>C
ENST00000677420.1:c.357T>C	ENSP00000504648.1:p.His119=
ENST00000677555.1:c.357T>C	ENSP00000503331.1:p.His119=
ENST00000677715.1:c.357T>C	ENSP00000502950.1:p.His119=
ENST00000677753.1:n.30T>C
ENST00000677961.1:n.60T>C
ENST00000678015.1:c.357T>C	ENSP00000502959.1:p.His119=
ENST00000678190.1:c.30T>C	ENSP00000503824.1:p.His10=
ENST00000678282.1:n.30T>C
ENST00000678297.1:c.357T>C	ENSP00000503472.1:p.His119=
ENST00000299697.11:c.648T>C	ENSP00000299697.8:p.His216=
ENST00000417693.7:c.720T>C	ENSP00000407469.4:p.His240=
ENST00000451102.6:c.774T>C	ENSP00000414334.3:p.His258=
ENST00000525974.5:c.357T>C	ENSP00000434594.1:p.His119=
ENST00000527284.5:c.555T>C	ENSP00000435312.1:p.His185=
ENST00000527800.5:c.357T>C	ENSP00000433770.1:p.His119=
ENST00000544898.5:c.648T>C	ENSP00000440898.2:p.His216=
ENST00000545043.6:c.573T>C	ENSP00000438143.2:p.His191=
ENST00000561527.5:n.207T>C
ENST00000561728.1:c.97T>C
ENST00000561905.2:c.2T>C
ENST00000562552.5:n.464T>C
ENST00000563099.5:n.175T>C
ENST00000563369.6:c.357T>C	ENSP00000463560.1:p.His119=
ENST00000563478.5:c.357T>C	ENSP00000462341.1:p.His119=
ENST00000564792.1:n.303T>C
ENST00000564917.5:c.699T>C	ENSP00000455187.1:p.His233=
ENST00000567357.5:c.*506T>C	ENSP00000457959.1:n.*506T>C
ENST00000569718.5:c.373T>C
ENST00000620035.4:c.594T>C	ENSP00000483833.1:p.His198=
NM_001172643.1:c.555T>C	NP_001166114.1:p.His185=
NM_001172644.1:c.573T>C	NP_001166115.1:p.His191=
NM_001172645.1:c.594T>C	NP_001166116.1:p.His198=
NM_001271934.1:c.501T>C	NP_001258863.1:p.His167=
NM_001271935.1:c.386T>C	NP_001258864.1:p.Met129Thr
NM_001272050.1:c.357T>C	NP_001258979.1:p.His119=
NM_004614.4:c.648T>C	NP_004605.4:p.His216=
NR_073520.1:n.1927T>C
NM_001172644.2:c.573T>C	NP_001166115.1:p.His191=
NM_001271934.2:c.501T>C	NP_001258863.1:p.His167=
NM_001272050.2:c.357T>C	NP_001258979.1:p.His119=
NM_004614.5:c.648T>C MANE Select	NP_004605.4:p.His216=
NR_073520.2:n.1637T>C
NM_001172645.2:c.594T>C	NP_001166116.1:p.His198=