Canonical Allele Identifier: CA396187161

Gene: TK2

Linked Data

• gnomAD v4: 16-66513767-G-C
• MyVariant Identifiers: chr16:g.66547670G>C (hg19) ; chr16:g.66513767G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66513767G>C , CM000678.2:g.66513767G>C	GRCh38
NC_000016.9:g.66547670G>C , CM000678.1:g.66547670G>C	GRCh37
NC_000016.8:g.65105171G>C	NCBI36
NG_016862.1:g.41646C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299697.12:c.495C>G	ENSP00000299697.9:p.Ile165Met
ENST00000417693.8:c.609C>G	ENSP00000407469.5:p.Ile203Met
ENST00000451102.7:c.570C>G	ENSP00000414334.4:p.Ile190Met
ENST00000527284.6:c.563-1701C>G
ENST00000527800.6:c.372C>G	ENSP00000433770.1:p.Ile124Met
ENST00000544898.6:c.663C>G MANE Select	ENSP00000440898.2:p.Ile221Met
ENST00000567357.6:c.*521C>G	ENSP00000457959.2:n.*521C>G
ENST00000569718.6:c.401C>G	ENSP00000464313.2:p.Ser134Ter
ENST00000620035.5:c.419C>G	ENSP00000483833.2:p.Ser140Ter
ENST00000676538.1:c.246C>G
ENST00000676904.1:c.134C>G
ENST00000677296.1:n.45C>G
ENST00000677379.1:c.304C>G	ENSP00000503672.1:n.304C>G
ENST00000677420.1:c.372C>G	ENSP00000504648.1:p.Ile124Met
ENST00000677555.1:c.372C>G	ENSP00000503331.1:p.Ile124Met
ENST00000677715.1:c.372C>G	ENSP00000502950.1:p.Ile124Met
ENST00000677753.1:n.45C>G
ENST00000677961.1:n.75C>G
ENST00000678015.1:c.372C>G	ENSP00000502959.1:p.Ile124Met
ENST00000678190.1:c.45C>G	ENSP00000503824.1:p.Ile15Met
ENST00000678282.1:n.45C>G
ENST00000678297.1:c.372C>G	ENSP00000503472.1:p.Ile124Met
ENST00000299697.11:c.663C>G	ENSP00000299697.8:p.Ile221Met
ENST00000417693.7:c.735C>G	ENSP00000407469.4:p.Ile245Met
ENST00000451102.6:c.789C>G	ENSP00000414334.3:p.Ile263Met
ENST00000525974.5:c.372C>G	ENSP00000434594.1:p.Ile124Met
ENST00000527284.5:c.570C>G	ENSP00000435312.1:p.Ile190Met
ENST00000527800.5:c.372C>G	ENSP00000433770.1:p.Ile124Met
ENST00000544898.5:c.663C>G	ENSP00000440898.2:p.Ile221Met
ENST00000545043.6:c.588C>G	ENSP00000438143.2:p.Ile196Met
ENST00000561527.5:n.222C>G
ENST00000561728.1:c.112C>G
ENST00000561905.2:c.17C>G
ENST00000562552.5:n.479C>G
ENST00000563099.5:n.190C>G
ENST00000563369.6:c.372C>G	ENSP00000463560.1:p.Ile124Met
ENST00000563478.5:c.372C>G	ENSP00000462341.1:p.Ile124Met
ENST00000564792.1:n.318C>G
ENST00000564917.5:c.714C>G	ENSP00000455187.1:p.Ile238Met
ENST00000567357.5:c.*521C>G	ENSP00000457959.1:n.*521C>G
ENST00000569718.5:c.388C>G
ENST00000620035.4:c.609C>G	ENSP00000483833.1:p.Ile203Met
NM_001172643.1:c.570C>G	NP_001166114.1:p.Ile190Met
NM_001172644.1:c.588C>G	NP_001166115.1:p.Ile196Met
NM_001172645.1:c.609C>G	NP_001166116.1:p.Ile203Met
NM_001271934.1:c.516C>G	NP_001258863.1:p.Ile172Met
NM_001271935.1:c.401C>G	NP_001258864.1:p.Ser134Ter
NM_001272050.1:c.372C>G	NP_001258979.1:p.Ile124Met
NM_004614.4:c.663C>G	NP_004605.4:p.Ile221Met
NR_073520.1:n.1942C>G
NM_001172644.2:c.588C>G	NP_001166115.1:p.Ile196Met
NM_001271934.2:c.516C>G	NP_001258863.1:p.Ile172Met
NM_001272050.2:c.372C>G	NP_001258979.1:p.Ile124Met
NM_004614.5:c.663C>G MANE Select	NP_004605.4:p.Ile221Met
NR_073520.2:n.1652C>G
NM_001172645.2:c.609C>G	NP_001166116.1:p.Ile203Met