Canonical Allele Identifier: CA622885410

Gene: TK2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66508683C>T , CM000678.2:g.66508683C>T	GRCh38
NC_000016.9:g.66542586C>T , CM000678.1:g.66542586C>T	GRCh37
NC_000016.8:g.65100087C>T	NCBI36
NG_016862.1:g.46730G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004614.5:c.*3285G>A MANE Select	NP_004605.4:n.*3285G>A
ENST00000544898.6:c.*3285G>A MANE Select	ENSP00000440898.2:n.*3285G>A
NM_001172643.1:c.*3285G>A	NP_001166114.1:n.*3285G>A
NM_001172644.1:c.*3285G>A	NP_001166115.1:n.*3285G>A
NM_001172644.2:c.*3285G>A	NP_001166115.1:n.*3285G>A
NM_001172645.1:c.*3285G>A	NP_001166116.1:n.*3285G>A
NM_001172645.2:c.*3285G>A	NP_001166116.1:n.*3285G>A
NM_001271934.1:c.*3285G>A	NP_001258863.1:n.*3285G>A
NM_001271934.2:c.*3285G>A	NP_001258863.1:n.*3285G>A
NM_001271935.1:c.*3380G>A	NP_001258864.1:n.*3380G>A
NM_001272050.1:c.*3285G>A	NP_001258979.1:n.*3285G>A
NM_001272050.2:c.*3285G>A	NP_001258979.1:n.*3285G>A
NM_004614.4:c.*3285G>A	NP_004605.4:n.*3285G>A
NR_073520.1:n.5362G>A
NR_073520.2:n.5072G>A
ENST00000299697.11:c.*3285G>A	ENSP00000299697.8:n.*3285G>A
ENST00000561527.5:n.258+5048G>A
ENST00000561728.1:c.148+5048G>A
ENST00000561905.2:c.142G>A
ENST00000620035.4:c.*3285G>A	ENSP00000483833.1:n.*3285G>A
ENST00000676821.1:n.89G>A
ENST00000677166.1:n.109+3275G>A
ENST00000677319.1:c.198G>A	ENSP00000503900.1:n.198G>A
ENST00000677405.1:n.89G>A
ENST00000677535.1:c.1545G>A	ENSP00000502856.1:n.1545G>A
ENST00000677668.1:n.89G>A
ENST00000677753.1:n.81+5048G>A
ENST00000678219.1:c.1433G>A	ENSP00000504142.1:n.1433G>A
ENST00000678257.1:n.89G>A
ENST00000678282.1:n.81+5048G>A