Canonical Allele Identifier: CA10648732

Gene: TK2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66531467G>A , CM000678.2:g.66531467G>A	GRCh38
NC_000016.9:g.66565370G>A , CM000678.1:g.66565370G>A	GRCh37
NC_000016.8:g.65122871G>A	NCBI36
NG_016862.1:g.23946C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299697.12:c.120C>T	ENSP00000299697.9:p.Gly40=
ENST00000417693.8:c.234C>T	ENSP00000407469.5:p.Gly78=
ENST00000451102.7:c.195C>T	ENSP00000414334.4:p.Gly65=
ENST00000527284.6:c.232C>T
ENST00000527800.6:c.-4C>T	ENSP00000433770.1:n.-4C>T
ENST00000544898.6:c.288C>T MANE Select	ENSP00000440898.2:p.Gly96=
ENST00000567357.6:c.*146C>T	ENSP00000457959.2:n.*146C>T
ENST00000569718.6:c.195C>T	ENSP00000464313.2:p.Gly65=
ENST00000620035.5:c.213C>T	ENSP00000483833.2:p.Gly71=
ENST00000676538.1:c.33-13590C>T
ENST00000677379.1:c.3C>T	ENSP00000503672.1:p.Gly1=
ENST00000677420.1:c.-4C>T	ENSP00000504648.1:n.-4C>T
ENST00000677497.1:n.175C>T
ENST00000677555.1:c.-4C>T	ENSP00000503331.1:n.-4C>T
ENST00000677715.1:c.-4C>T	ENSP00000502950.1:n.-4C>T
ENST00000677739.1:c.55-2400C>T	ENSP00000504644.1:n.55-2400C>T
ENST00000678015.1:c.-4C>T	ENSP00000502959.1:n.-4C>T
ENST00000678297.1:c.-4C>T	ENSP00000503472.1:n.-4C>T
ENST00000678314.1:c.-4C>T	ENSP00000504438.1:n.-4C>T
ENST00000678746.1:c.178C>T	ENSP00000503227.1:n.178C>T
ENST00000679154.1:c.35C>T
ENST00000299697.11:c.288C>T	ENSP00000299697.8:p.Gly96=
ENST00000417693.7:c.360C>T	ENSP00000407469.4:p.Gly120=
ENST00000451102.6:c.414C>T	ENSP00000414334.3:p.Gly138=
ENST00000525974.5:c.-4C>T	ENSP00000434594.1:n.-4C>T
ENST00000527284.5:c.195C>T	ENSP00000435312.1:p.Gly65=
ENST00000527800.5:c.-4C>T	ENSP00000433770.1:n.-4C>T
ENST00000544898.5:c.288C>T	ENSP00000440898.2:p.Gly96=
ENST00000545043.6:c.213C>T	ENSP00000438143.2:p.Gly71=
ENST00000562484.2:c.-4C>T	ENSP00000463326.1:n.-4C>T
ENST00000563369.6:c.-4C>T	ENSP00000463560.1:n.-4C>T
ENST00000563478.5:c.-4C>T	ENSP00000462341.1:n.-4C>T
ENST00000564917.5:c.288C>T	ENSP00000455187.1:p.Gly96=
ENST00000567357.5:c.*146C>T	ENSP00000457959.1:n.*146C>T
ENST00000569718.5:c.182C>T
ENST00000620035.4:c.234C>T	ENSP00000483833.1:p.Gly78=
NM_001172643.1:c.195C>T	NP_001166114.1:p.Gly65=
NM_001172644.1:c.213C>T	NP_001166115.1:p.Gly71=
NM_001172645.1:c.234C>T	NP_001166116.1:p.Gly78=
NM_001271934.1:c.141C>T	NP_001258863.1:p.Gly47=
NM_001271935.1:c.195C>T	NP_001258864.1:p.Gly65=
NM_001272050.1:c.-4C>T	NP_001258979.1:n.-4C>T
NM_004614.4:c.288C>T	NP_004605.4:p.Gly96=
NR_073520.1:n.1567C>T
NM_001172644.2:c.213C>T	NP_001166115.1:p.Gly71=
NM_001271934.2:c.141C>T	NP_001258863.1:p.Gly47=
NM_001272050.2:c.-4C>T	NP_001258979.1:n.-4C>T
NM_004614.5:c.288C>T MANE Select	NP_004605.4:p.Gly96=
NR_073520.2:n.1277C>T
NM_001172645.2:c.234C>T	NP_001166116.1:p.Gly78=