Canonical Allele Identifier: CA8093653

Gene: TK2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66517808G>A , CM000678.2:g.66517808G>A	GRCh38
NC_000016.9:g.66551711G>A , CM000678.1:g.66551711G>A	GRCh37
NC_000016.8:g.65109212G>A	NCBI36
NG_016862.1:g.37605C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299697.12:c.351C>T	ENSP00000299697.9:p.Asp117=
ENST00000417693.8:c.465C>T	ENSP00000407469.5:p.Asp155=
ENST00000451102.7:c.426C>T	ENSP00000414334.4:p.Asp142=
ENST00000527284.6:c.463C>T
ENST00000527800.6:c.228C>T	ENSP00000433770.1:p.Asp76=
ENST00000544898.6:c.519C>T MANE Select	ENSP00000440898.2:p.Asp173=
ENST00000567357.6:c.*377C>T	ENSP00000457959.2:n.*377C>T
ENST00000569718.6:c.357-3997C>T	ENSP00000464313.2:n.357-3997C>T
ENST00000620035.5:c.375-3997C>T	ENSP00000483833.2:n.375-3997C>T
ENST00000676538.1:c.102C>T
ENST00000676718.1:n.100C>T
ENST00000676904.1:c.70C>T
ENST00000677379.1:c.160C>T	ENSP00000503672.1:n.160C>T
ENST00000677420.1:c.228C>T	ENSP00000504648.1:p.Asp76=
ENST00000677555.1:c.228C>T	ENSP00000503331.1:p.Asp76=
ENST00000677715.1:c.228C>T	ENSP00000502950.1:p.Asp76=
ENST00000678015.1:c.228C>T	ENSP00000502959.1:p.Asp76=
ENST00000678297.1:c.228C>T	ENSP00000503472.1:p.Asp76=
ENST00000678314.1:c.228C>T	ENSP00000504438.1:p.Asp76=
ENST00000679306.1:n.100C>T
ENST00000299697.11:c.519C>T	ENSP00000299697.8:p.Asp173=
ENST00000417693.7:c.591C>T	ENSP00000407469.4:p.Asp197=
ENST00000451102.6:c.645C>T	ENSP00000414334.3:p.Asp215=
ENST00000525974.5:c.228C>T	ENSP00000434594.1:p.Asp76=
ENST00000527284.5:c.426C>T	ENSP00000435312.1:p.Asp142=
ENST00000527800.5:c.228C>T	ENSP00000433770.1:p.Asp76=
ENST00000544898.5:c.519C>T	ENSP00000440898.2:p.Asp173=
ENST00000545043.6:c.444C>T	ENSP00000438143.2:p.Asp148=
ENST00000562484.2:c.228C>T	ENSP00000463326.1:p.Asp76=
ENST00000562552.5:n.335C>T
ENST00000563369.6:c.228C>T	ENSP00000463560.1:p.Asp76=
ENST00000563478.5:c.228C>T	ENSP00000462341.1:p.Asp76=
ENST00000564792.1:n.174C>T
ENST00000564917.5:c.519C>T	ENSP00000455187.1:p.Asp173=
ENST00000567357.5:c.*377C>T	ENSP00000457959.1:n.*377C>T
ENST00000569718.5:c.344-3997C>T
ENST00000620035.4:c.465C>T	ENSP00000483833.1:p.Asp155=
NM_001172643.1:c.426C>T	NP_001166114.1:p.Asp142=
NM_001172644.1:c.444C>T	NP_001166115.1:p.Asp148=
NM_001172645.1:c.465C>T	NP_001166116.1:p.Asp155=
NM_001271934.1:c.372C>T	NP_001258863.1:p.Asp124=
NM_001271935.1:c.357-3997C>T	NP_001258864.1:n.357-3997C>T
NM_001272050.1:c.228C>T	NP_001258979.1:p.Asp76=
NM_004614.4:c.519C>T	NP_004605.4:p.Asp173=
NR_073520.1:n.1798C>T
NM_001172644.2:c.444C>T	NP_001166115.1:p.Asp148=
NM_001271934.2:c.372C>T	NP_001258863.1:p.Asp124=
NM_001272050.2:c.228C>T	NP_001258979.1:p.Asp76=
NM_004614.5:c.519C>T MANE Select	NP_004605.4:p.Asp173=
NR_073520.2:n.1508C>T
NM_001172645.2:c.465C>T	NP_001166116.1:p.Asp155=