Canonical Allele Identifier: CA396187135

Gene: TK2

Linked Data

• dbSNP Id: rs779465340
• gnomAD v3: 16-66513762-C-G
• gnomAD v4: 16-66513762-C-G
• MyVariant Identifiers: chr16:g.66547665C>G (hg19) ; chr16:g.66513762C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66513762C>G , CM000678.2:g.66513762C>G	GRCh38
NC_000016.9:g.66547665C>G , CM000678.1:g.66547665C>G	GRCh37
NC_000016.8:g.65105166C>G	NCBI36
NG_016862.1:g.41651G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299697.12:c.500G>C	ENSP00000299697.9:p.Gly167Ala
ENST00000417693.8:c.614G>C	ENSP00000407469.5:p.Gly205Ala
ENST00000451102.7:c.575G>C	ENSP00000414334.4:p.Gly192Ala
ENST00000527284.6:c.563-1696G>C
ENST00000527800.6:c.377G>C	ENSP00000433770.1:p.Gly126Ala
ENST00000544898.6:c.668G>C MANE Select	ENSP00000440898.2:p.Gly223Ala
ENST00000567357.6:c.*526G>C	ENSP00000457959.2:n.*526G>C
ENST00000569718.6:c.406G>C	ENSP00000464313.2:p.Ala136Pro
ENST00000620035.5:c.424G>C	ENSP00000483833.2:p.Ala142Pro
ENST00000676538.1:c.251G>C
ENST00000676904.1:c.139G>C
ENST00000677296.1:n.50G>C
ENST00000677379.1:c.309G>C	ENSP00000503672.1:n.309G>C
ENST00000677420.1:c.377G>C	ENSP00000504648.1:p.Gly126Ala
ENST00000677555.1:c.377G>C	ENSP00000503331.1:p.Gly126Ala
ENST00000677715.1:c.377G>C	ENSP00000502950.1:p.Gly126Ala
ENST00000677753.1:n.50G>C
ENST00000677961.1:n.80G>C
ENST00000678015.1:c.377G>C	ENSP00000502959.1:p.Gly126Ala
ENST00000678190.1:c.50G>C	ENSP00000503824.1:p.Gly17Ala
ENST00000678282.1:n.50G>C
ENST00000678297.1:c.377G>C	ENSP00000503472.1:p.Gly126Ala
ENST00000299697.11:c.668G>C	ENSP00000299697.8:p.Gly223Ala
ENST00000417693.7:c.740G>C	ENSP00000407469.4:p.Gly247Ala
ENST00000451102.6:c.794G>C	ENSP00000414334.3:p.Gly265Ala
ENST00000525974.5:c.377G>C	ENSP00000434594.1:p.Gly126Ala
ENST00000527284.5:c.575G>C	ENSP00000435312.1:p.Gly192Ala
ENST00000527800.5:c.377G>C	ENSP00000433770.1:p.Gly126Ala
ENST00000544898.5:c.668G>C	ENSP00000440898.2:p.Gly223Ala
ENST00000545043.6:c.593G>C	ENSP00000438143.2:p.Gly198Ala
ENST00000561527.5:n.227G>C
ENST00000561728.1:c.117G>C
ENST00000561905.2:c.22G>C
ENST00000562552.5:n.484G>C
ENST00000563099.5:n.195G>C
ENST00000563369.6:c.377G>C	ENSP00000463560.1:p.Gly126Ala
ENST00000563478.5:c.377G>C	ENSP00000462341.1:p.Gly126Ala
ENST00000564792.1:n.323G>C
ENST00000564917.5:c.719G>C	ENSP00000455187.1:p.Gly240Ala
ENST00000567357.5:c.*526G>C	ENSP00000457959.1:n.*526G>C
ENST00000569718.5:c.393G>C
ENST00000620035.4:c.614G>C	ENSP00000483833.1:p.Gly205Ala
NM_001172643.1:c.575G>C	NP_001166114.1:p.Gly192Ala
NM_001172644.1:c.593G>C	NP_001166115.1:p.Gly198Ala
NM_001172645.1:c.614G>C	NP_001166116.1:p.Gly205Ala
NM_001271934.1:c.521G>C	NP_001258863.1:p.Gly174Ala
NM_001271935.1:c.406G>C	NP_001258864.1:p.Ala136Pro
NM_001272050.1:c.377G>C	NP_001258979.1:p.Gly126Ala
NM_004614.4:c.668G>C	NP_004605.4:p.Gly223Ala
NR_073520.1:n.1947G>C
NM_001172644.2:c.593G>C	NP_001166115.1:p.Gly198Ala
NM_001271934.2:c.521G>C	NP_001258863.1:p.Gly174Ala
NM_001272050.2:c.377G>C	NP_001258979.1:p.Gly126Ala
NM_004614.5:c.668G>C MANE Select	NP_004605.4:p.Gly223Ala
NR_073520.2:n.1657G>C
NM_001172645.2:c.614G>C	NP_001166116.1:p.Gly205Ala