Canonical Allele Identifier: CA396187166

Gene: TK2

Linked Data

• MyVariant Identifiers: chr16:g.66547671A>G (hg19) ; chr16:g.66513768A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66513768A>G , CM000678.2:g.66513768A>G	GRCh38
NC_000016.9:g.66547671A>G , CM000678.1:g.66547671A>G	GRCh37
NC_000016.8:g.65105172A>G	NCBI36
NG_016862.1:g.41645T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299697.12:c.494T>C	ENSP00000299697.9:p.Ile165Thr
ENST00000417693.8:c.608T>C	ENSP00000407469.5:p.Ile203Thr
ENST00000451102.7:c.569T>C	ENSP00000414334.4:p.Ile190Thr
ENST00000527284.6:c.563-1702T>C
ENST00000527800.6:c.371T>C	ENSP00000433770.1:p.Ile124Thr
ENST00000544898.6:c.662T>C MANE Select	ENSP00000440898.2:p.Ile221Thr
ENST00000567357.6:c.*520T>C	ENSP00000457959.2:n.*520T>C
ENST00000569718.6:c.400T>C	ENSP00000464313.2:p.Ser134Pro
ENST00000620035.5:c.418T>C	ENSP00000483833.2:p.Ser140Pro
ENST00000676538.1:c.245T>C
ENST00000676904.1:c.133T>C
ENST00000677296.1:n.44T>C
ENST00000677379.1:c.303T>C	ENSP00000503672.1:n.303T>C
ENST00000677420.1:c.371T>C	ENSP00000504648.1:p.Ile124Thr
ENST00000677555.1:c.371T>C	ENSP00000503331.1:p.Ile124Thr
ENST00000677715.1:c.371T>C	ENSP00000502950.1:p.Ile124Thr
ENST00000677753.1:n.44T>C
ENST00000677961.1:n.74T>C
ENST00000678015.1:c.371T>C	ENSP00000502959.1:p.Ile124Thr
ENST00000678190.1:c.44T>C	ENSP00000503824.1:p.Ile15Thr
ENST00000678282.1:n.44T>C
ENST00000678297.1:c.371T>C	ENSP00000503472.1:p.Ile124Thr
ENST00000299697.11:c.662T>C	ENSP00000299697.8:p.Ile221Thr
ENST00000417693.7:c.734T>C	ENSP00000407469.4:p.Ile245Thr
ENST00000451102.6:c.788T>C	ENSP00000414334.3:p.Ile263Thr
ENST00000525974.5:c.371T>C	ENSP00000434594.1:p.Ile124Thr
ENST00000527284.5:c.569T>C	ENSP00000435312.1:p.Ile190Thr
ENST00000527800.5:c.371T>C	ENSP00000433770.1:p.Ile124Thr
ENST00000544898.5:c.662T>C	ENSP00000440898.2:p.Ile221Thr
ENST00000545043.6:c.587T>C	ENSP00000438143.2:p.Ile196Thr
ENST00000561527.5:n.221T>C
ENST00000561728.1:c.111T>C
ENST00000561905.2:c.16T>C
ENST00000562552.5:n.478T>C
ENST00000563099.5:n.189T>C
ENST00000563369.6:c.371T>C	ENSP00000463560.1:p.Ile124Thr
ENST00000563478.5:c.371T>C	ENSP00000462341.1:p.Ile124Thr
ENST00000564792.1:n.317T>C
ENST00000564917.5:c.713T>C	ENSP00000455187.1:p.Ile238Thr
ENST00000567357.5:c.*520T>C	ENSP00000457959.1:n.*520T>C
ENST00000569718.5:c.387T>C
ENST00000620035.4:c.608T>C	ENSP00000483833.1:p.Ile203Thr
NM_001172643.1:c.569T>C	NP_001166114.1:p.Ile190Thr
NM_001172644.1:c.587T>C	NP_001166115.1:p.Ile196Thr
NM_001172645.1:c.608T>C	NP_001166116.1:p.Ile203Thr
NM_001271934.1:c.515T>C	NP_001258863.1:p.Ile172Thr
NM_001271935.1:c.400T>C	NP_001258864.1:p.Ser134Pro
NM_001272050.1:c.371T>C	NP_001258979.1:p.Ile124Thr
NM_004614.4:c.662T>C	NP_004605.4:p.Ile221Thr
NR_073520.1:n.1941T>C
NM_001172644.2:c.587T>C	NP_001166115.1:p.Ile196Thr
NM_001271934.2:c.515T>C	NP_001258863.1:p.Ile172Thr
NM_001272050.2:c.371T>C	NP_001258979.1:p.Ile124Thr
NM_004614.5:c.662T>C MANE Select	NP_004605.4:p.Ile221Thr
NR_073520.2:n.1651T>C
NM_001172645.2:c.608T>C	NP_001166116.1:p.Ile203Thr