Canonical Allele Identifier: CA396187474

Gene: TK2

Linked Data

• MyVariant Identifiers: chr16:g.66547741C>G (hg19) ; chr16:g.66513838C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66513838C>G , CM000678.2:g.66513838C>G	GRCh38
NC_000016.9:g.66547741C>G , CM000678.1:g.66547741C>G	GRCh37
NC_000016.8:g.65105242C>G	NCBI36
NG_016862.1:g.41575G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299697.12:c.451-27G>C	ENSP00000299697.9:n.451-27G>C
ENST00000417693.8:c.565-27G>C	ENSP00000407469.5:n.565-27G>C
ENST00000451102.7:c.526-27G>C	ENSP00000414334.4:n.526-27G>C
ENST00000527284.6:c.563-1772G>C
ENST00000527800.6:c.328-27G>C	ENSP00000433770.1:n.328-27G>C
ENST00000544898.6:c.619-27G>C MANE Select	ENSP00000440898.2:n.619-27G>C
ENST00000567357.6:c.*477-27G>C	ENSP00000457959.2:n.*477-27G>C
ENST00000569718.6:c.357-27G>C	ENSP00000464313.2:n.357-27G>C
ENST00000620035.5:c.375-27G>C	ENSP00000483833.2:n.375-27G>C
ENST00000676538.1:c.202-27G>C
ENST00000676904.1:c.90-27G>C
ENST00000677379.1:c.260-27G>C	ENSP00000503672.1:n.260-27G>C
ENST00000677420.1:c.328-27G>C	ENSP00000504648.1:n.328-27G>C
ENST00000677555.1:c.328-27G>C	ENSP00000503331.1:n.328-27G>C
ENST00000677715.1:c.328-27G>C	ENSP00000502950.1:n.328-27G>C
ENST00000677961.1:n.31-27G>C
ENST00000678015.1:c.328-27G>C	ENSP00000502959.1:n.328-27G>C
ENST00000678297.1:c.328-27G>C	ENSP00000503472.1:n.328-27G>C
ENST00000299697.11:c.619-27G>C	ENSP00000299697.8:n.619-27G>C
ENST00000417693.7:c.691-27G>C	ENSP00000407469.4:n.691-27G>C
ENST00000451102.6:c.745-27G>C	ENSP00000414334.3:n.745-27G>C
ENST00000525974.5:c.328-27G>C	ENSP00000434594.1:n.328-27G>C
ENST00000527284.5:c.526-27G>C	ENSP00000435312.1:n.526-27G>C
ENST00000527800.5:c.328-27G>C	ENSP00000433770.1:n.328-27G>C
ENST00000544898.5:c.619-27G>C	ENSP00000440898.2:n.619-27G>C
ENST00000545043.6:c.544-27G>C	ENSP00000438143.2:n.544-27G>C
ENST00000561527.5:n.178-27G>C
ENST00000561728.1:c.68-27G>C
ENST00000562552.5:n.435-27G>C
ENST00000563099.5:n.146-27G>C
ENST00000563369.6:c.328-27G>C	ENSP00000463560.1:n.328-27G>C
ENST00000563478.5:c.328-27G>C	ENSP00000462341.1:n.328-27G>C
ENST00000564792.1:n.274-27G>C
ENST00000564917.5:c.643G>C	ENSP00000455187.1:p.Asp215His
ENST00000567357.5:c.*477-27G>C	ENSP00000457959.1:n.*477-27G>C
ENST00000569718.5:c.344-27G>C
ENST00000620035.4:c.565-27G>C	ENSP00000483833.1:n.565-27G>C
NM_001172643.1:c.526-27G>C	NP_001166114.1:n.526-27G>C
NM_001172644.1:c.544-27G>C	NP_001166115.1:n.544-27G>C
NM_001172645.1:c.565-27G>C	NP_001166116.1:n.565-27G>C
NM_001271934.1:c.472-27G>C	NP_001258863.1:n.472-27G>C
NM_001271935.1:c.357-27G>C	NP_001258864.1:n.357-27G>C
NM_001272050.1:c.328-27G>C	NP_001258979.1:n.328-27G>C
NM_004614.4:c.619-27G>C	NP_004605.4:n.619-27G>C
NR_073520.1:n.1898-27G>C
NM_001172644.2:c.544-27G>C	NP_001166115.1:n.544-27G>C
NM_001271934.2:c.472-27G>C	NP_001258863.1:n.472-27G>C
NM_001272050.2:c.328-27G>C	NP_001258979.1:n.328-27G>C
NM_004614.5:c.619-27G>C MANE Select	NP_004605.4:n.619-27G>C
NR_073520.2:n.1608-27G>C
NM_001172645.2:c.565-27G>C	NP_001166116.1:n.565-27G>C