Canonical Allele Identifier: CA396187252

Gene: TK2

Linked Data

• MyVariant Identifiers: chr16:g.66547687G>C (hg19) ; chr16:g.66513784G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66513784G>C , CM000678.2:g.66513784G>C	GRCh38
NC_000016.9:g.66547687G>C , CM000678.1:g.66547687G>C	GRCh37
NC_000016.8:g.65105188G>C	NCBI36
NG_016862.1:g.41629C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299697.12:c.478C>G	ENSP00000299697.9:p.His160Asp
ENST00000417693.8:c.592C>G	ENSP00000407469.5:p.His198Asp
ENST00000451102.7:c.553C>G	ENSP00000414334.4:p.His185Asp
ENST00000527284.6:c.563-1718C>G
ENST00000527800.6:c.355C>G	ENSP00000433770.1:p.His119Asp
ENST00000544898.6:c.646C>G MANE Select	ENSP00000440898.2:p.His216Asp
ENST00000567357.6:c.*504C>G	ENSP00000457959.2:n.*504C>G
ENST00000569718.6:c.384C>G	ENSP00000464313.2:p.Ser128=
ENST00000620035.5:c.402C>G	ENSP00000483833.2:p.Ser134=
ENST00000676538.1:c.229C>G
ENST00000676904.1:c.117C>G
ENST00000677296.1:n.28C>G
ENST00000677379.1:c.287C>G	ENSP00000503672.1:n.287C>G
ENST00000677420.1:c.355C>G	ENSP00000504648.1:p.His119Asp
ENST00000677555.1:c.355C>G	ENSP00000503331.1:p.His119Asp
ENST00000677715.1:c.355C>G	ENSP00000502950.1:p.His119Asp
ENST00000677753.1:n.28C>G
ENST00000677961.1:n.58C>G
ENST00000678015.1:c.355C>G	ENSP00000502959.1:p.His119Asp
ENST00000678190.1:c.28C>G	ENSP00000503824.1:p.His10Asp
ENST00000678282.1:n.28C>G
ENST00000678297.1:c.355C>G	ENSP00000503472.1:p.His119Asp
ENST00000299697.11:c.646C>G	ENSP00000299697.8:p.His216Asp
ENST00000417693.7:c.718C>G	ENSP00000407469.4:p.His240Asp
ENST00000451102.6:c.772C>G	ENSP00000414334.3:p.His258Asp
ENST00000525974.5:c.355C>G	ENSP00000434594.1:p.His119Asp
ENST00000527284.5:c.553C>G	ENSP00000435312.1:p.His185Asp
ENST00000527800.5:c.355C>G	ENSP00000433770.1:p.His119Asp
ENST00000544898.5:c.646C>G	ENSP00000440898.2:p.His216Asp
ENST00000545043.6:c.571C>G	ENSP00000438143.2:p.His191Asp
ENST00000561527.5:n.205C>G
ENST00000561728.1:c.95C>G
ENST00000562552.5:n.462C>G
ENST00000563099.5:n.173C>G
ENST00000563369.6:c.355C>G	ENSP00000463560.1:p.His119Asp
ENST00000563478.5:c.355C>G	ENSP00000462341.1:p.His119Asp
ENST00000564792.1:n.301C>G
ENST00000564917.5:c.697C>G	ENSP00000455187.1:p.His233Asp
ENST00000567357.5:c.*504C>G	ENSP00000457959.1:n.*504C>G
ENST00000569718.5:c.371C>G
ENST00000620035.4:c.592C>G	ENSP00000483833.1:p.His198Asp
NM_001172643.1:c.553C>G	NP_001166114.1:p.His185Asp
NM_001172644.1:c.571C>G	NP_001166115.1:p.His191Asp
NM_001172645.1:c.592C>G	NP_001166116.1:p.His198Asp
NM_001271934.1:c.499C>G	NP_001258863.1:p.His167Asp
NM_001271935.1:c.384C>G	NP_001258864.1:p.Ser128=
NM_001272050.1:c.355C>G	NP_001258979.1:p.His119Asp
NM_004614.4:c.646C>G	NP_004605.4:p.His216Asp
NR_073520.1:n.1925C>G
NM_001172644.2:c.571C>G	NP_001166115.1:p.His191Asp
NM_001271934.2:c.499C>G	NP_001258863.1:p.His167Asp
NM_001272050.2:c.355C>G	NP_001258979.1:p.His119Asp
NM_004614.5:c.646C>G MANE Select	NP_004605.4:p.His216Asp
NR_073520.2:n.1635C>G
NM_001172645.2:c.592C>G	NP_001166116.1:p.His198Asp