Canonical Allele Identifier: CA495902951

Gene: TK2

Linked Data

• dbSNP Id: rs1964520683
• MyVariant Identifiers: chr16:g.66547655G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66513752G>A , CM000678.2:g.66513752G>A	GRCh38
NC_000016.9:g.66547655G>A , CM000678.1:g.66547655G>A	GRCh37
NC_000016.8:g.65105156G>A	NCBI36
NG_016862.1:g.41661C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299697.12:c.510C>T	ENSP00000299697.9:p.Phe170=
ENST00000417693.8:c.624C>T	ENSP00000407469.5:p.Phe208=
ENST00000451102.7:c.585C>T	ENSP00000414334.4:p.Phe195=
ENST00000527284.6:c.563-1686C>T
ENST00000527800.6:c.387C>T	ENSP00000433770.1:p.Phe129=
ENST00000544898.6:c.678C>T MANE Select	ENSP00000440898.2:p.Phe226=
ENST00000567357.6:c.*536C>T	ENSP00000457959.2:n.*536C>T
ENST00000569718.6:c.416C>T	ENSP00000464313.2:p.Ser139Phe
ENST00000620035.5:c.434C>T	ENSP00000483833.2:p.Ser145Phe
ENST00000676538.1:c.261C>T
ENST00000676904.1:c.149C>T
ENST00000677296.1:n.60C>T
ENST00000677379.1:c.319C>T	ENSP00000503672.1:n.319C>T
ENST00000677420.1:c.387C>T	ENSP00000504648.1:p.Phe129=
ENST00000677555.1:c.387C>T	ENSP00000503331.1:p.Phe129=
ENST00000677715.1:c.387C>T	ENSP00000502950.1:p.Phe129=
ENST00000677753.1:n.60C>T
ENST00000677961.1:n.90C>T
ENST00000678015.1:c.387C>T	ENSP00000502959.1:p.Phe129=
ENST00000678190.1:c.60C>T	ENSP00000503824.1:p.Phe20=
ENST00000678282.1:n.60C>T
ENST00000678297.1:c.387C>T	ENSP00000503472.1:p.Phe129=
ENST00000299697.11:c.678C>T	ENSP00000299697.8:p.Phe226=
ENST00000417693.7:c.750C>T	ENSP00000407469.4:p.Phe250=
ENST00000451102.6:c.804C>T	ENSP00000414334.3:p.Phe268=
ENST00000525974.5:c.387C>T	ENSP00000434594.1:p.Phe129=
ENST00000527284.5:c.585C>T	ENSP00000435312.1:p.Phe195=
ENST00000527800.5:c.387C>T	ENSP00000433770.1:p.Phe129=
ENST00000544898.5:c.678C>T	ENSP00000440898.2:p.Phe226=
ENST00000545043.6:c.603C>T	ENSP00000438143.2:p.Phe201=
ENST00000561527.5:n.237C>T
ENST00000561728.1:c.127C>T
ENST00000561905.2:c.32C>T
ENST00000562552.5:n.494C>T
ENST00000563099.5:n.205C>T
ENST00000563369.6:c.387C>T	ENSP00000463560.1:p.Phe129=
ENST00000563478.5:c.387C>T	ENSP00000462341.1:p.Phe129=
ENST00000564792.1:n.333C>T
ENST00000564917.5:c.729C>T	ENSP00000455187.1:p.Phe243=
ENST00000567357.5:c.*536C>T	ENSP00000457959.1:n.*536C>T
ENST00000569718.5:c.403C>T
ENST00000620035.4:c.624C>T	ENSP00000483833.1:p.Phe208=
NM_001172643.1:c.585C>T	NP_001166114.1:p.Phe195=
NM_001172644.1:c.603C>T	NP_001166115.1:p.Phe201=
NM_001172645.1:c.624C>T	NP_001166116.1:p.Phe208=
NM_001271934.1:c.531C>T	NP_001258863.1:p.Phe177=
NM_001271935.1:c.416C>T	NP_001258864.1:p.Ser139Phe
NM_001272050.1:c.387C>T	NP_001258979.1:p.Phe129=
NM_004614.4:c.678C>T	NP_004605.4:p.Phe226=
NR_073520.1:n.1957C>T
NM_001172644.2:c.603C>T	NP_001166115.1:p.Phe201=
NM_001271934.2:c.531C>T	NP_001258863.1:p.Phe177=
NM_001272050.2:c.387C>T	NP_001258979.1:p.Phe129=
NM_004614.5:c.678C>T MANE Select	NP_004605.4:p.Phe226=
NR_073520.2:n.1667C>T
NM_001172645.2:c.624C>T	NP_001166116.1:p.Phe208=