Canonical Allele Identifier: CA495905514

Gene: TK2

Linked Data

• gnomAD v4: 16-66529065-C-A
• MyVariant Identifiers: chr16:g.66562968C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66529065C>A , CM000678.2:g.66529065C>A	GRCh38
NC_000016.9:g.66562968C>A , CM000678.1:g.66562968C>A	GRCh37
NC_000016.8:g.65120469C>A	NCBI36
NG_016862.1:g.26348G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299697.12:c.210G>T	ENSP00000299697.9:p.Val70=
ENST00000417693.8:c.324G>T	ENSP00000407469.5:p.Val108=
ENST00000451102.7:c.285G>T	ENSP00000414334.4:p.Val95=
ENST00000527284.6:c.322G>T
ENST00000527800.6:c.87G>T	ENSP00000433770.1:p.Val29=
ENST00000544898.6:c.378G>T MANE Select	ENSP00000440898.2:p.Val126=
ENST00000567357.6:c.*236G>T	ENSP00000457959.2:n.*236G>T
ENST00000569718.6:c.285G>T	ENSP00000464313.2:p.Val95=
ENST00000620035.5:c.303G>T	ENSP00000483833.2:p.Val101=
ENST00000676538.1:c.33-11188G>T
ENST00000677379.1:c.90+2315G>T	ENSP00000503672.1:n.90+2315G>T
ENST00000677420.1:c.87G>T	ENSP00000504648.1:p.Val29=
ENST00000677555.1:c.87G>T	ENSP00000503331.1:p.Val29=
ENST00000677715.1:c.87G>T	ENSP00000502950.1:p.Val29=
ENST00000677739.1:c.57G>T	ENSP00000504644.1:p.Val19=
ENST00000678015.1:c.87G>T	ENSP00000502959.1:p.Val29=
ENST00000678297.1:c.87G>T	ENSP00000503472.1:p.Val29=
ENST00000678314.1:c.87G>T	ENSP00000504438.1:p.Val29=
ENST00000678746.1:c.268G>T	ENSP00000503227.1:n.268G>T
ENST00000299697.11:c.378G>T	ENSP00000299697.8:p.Val126=
ENST00000417693.7:c.450G>T	ENSP00000407469.4:p.Val150=
ENST00000451102.6:c.504G>T	ENSP00000414334.3:p.Val168=
ENST00000525974.5:c.87G>T	ENSP00000434594.1:p.Val29=
ENST00000527284.5:c.285G>T	ENSP00000435312.1:p.Val95=
ENST00000527800.5:c.87G>T	ENSP00000433770.1:p.Val29=
ENST00000544898.5:c.378G>T	ENSP00000440898.2:p.Val126=
ENST00000545043.6:c.303G>T	ENSP00000438143.2:p.Val101=
ENST00000562484.2:c.87G>T	ENSP00000463326.1:p.Val29=
ENST00000563369.6:c.87G>T	ENSP00000463560.1:p.Val29=
ENST00000563478.5:c.87G>T	ENSP00000462341.1:p.Val29=
ENST00000564917.5:c.378G>T	ENSP00000455187.1:p.Val126=
ENST00000567357.5:c.*236G>T	ENSP00000457959.1:n.*236G>T
ENST00000569718.5:c.272G>T
ENST00000620035.4:c.324G>T	ENSP00000483833.1:p.Val108=
NM_001172643.1:c.285G>T	NP_001166114.1:p.Val95=
NM_001172644.1:c.303G>T	NP_001166115.1:p.Val101=
NM_001172645.1:c.324G>T	NP_001166116.1:p.Val108=
NM_001271934.1:c.231G>T	NP_001258863.1:p.Val77=
NM_001271935.1:c.285G>T	NP_001258864.1:p.Val95=
NM_001272050.1:c.87G>T	NP_001258979.1:p.Val29=
NM_004614.4:c.378G>T	NP_004605.4:p.Val126=
NR_073520.1:n.1657G>T
NM_001172644.2:c.303G>T	NP_001166115.1:p.Val101=
NM_001271934.2:c.231G>T	NP_001258863.1:p.Val77=
NM_001272050.2:c.87G>T	NP_001258979.1:p.Val29=
NM_004614.5:c.378G>T MANE Select	NP_004605.4:p.Val126=
NR_073520.2:n.1367G>T
NM_001172645.2:c.324G>T	NP_001166116.1:p.Val108=