Canonical Allele Identifier: CA396190635

Gene: TK2

Linked Data

• MyVariant Identifiers: chr16:g.66565341C>A (hg19) ; chr16:g.66531438C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66531438C>A , CM000678.2:g.66531438C>A	GRCh38
NC_000016.9:g.66565341C>A , CM000678.1:g.66565341C>A	GRCh37
NC_000016.8:g.65122842C>A	NCBI36
NG_016862.1:g.23975G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000299697.12:c.149G>T	ENSP00000299697.9:p.Gly50Val
ENST00000417693.8:c.263G>T	ENSP00000407469.5:p.Gly88Val
ENST00000451102.7:c.224G>T	ENSP00000414334.4:p.Gly75Val
ENST00000527284.6:c.261G>T
ENST00000527800.6:c.26G>T	ENSP00000433770.1:p.Gly9Val
ENST00000544898.6:c.317G>T MANE Select	ENSP00000440898.2:p.Gly106Val
ENST00000567357.6:c.*175G>T	ENSP00000457959.2:n.*175G>T
ENST00000569718.6:c.224G>T	ENSP00000464313.2:p.Gly75Val
ENST00000620035.5:c.242G>T	ENSP00000483833.2:p.Gly81Val
ENST00000676538.1:c.33-13561G>T
ENST00000677379.1:c.32G>T	ENSP00000503672.1:p.Gly11Val
ENST00000677420.1:c.26G>T	ENSP00000504648.1:p.Gly9Val
ENST00000677497.1:n.204G>T
ENST00000677555.1:c.26G>T	ENSP00000503331.1:p.Gly9Val
ENST00000677715.1:c.26G>T	ENSP00000502950.1:p.Gly9Val
ENST00000677739.1:c.55-2371G>T	ENSP00000504644.1:n.55-2371G>T
ENST00000678015.1:c.26G>T	ENSP00000502959.1:p.Gly9Val
ENST00000678297.1:c.26G>T	ENSP00000503472.1:p.Gly9Val
ENST00000678314.1:c.26G>T	ENSP00000504438.1:p.Gly9Val
ENST00000678746.1:c.207G>T	ENSP00000503227.1:n.207G>T
ENST00000679154.1:c.64G>T
ENST00000299697.11:c.317G>T	ENSP00000299697.8:p.Gly106Val
ENST00000417693.7:c.389G>T	ENSP00000407469.4:p.Gly130Val
ENST00000451102.6:c.443G>T	ENSP00000414334.3:p.Gly148Val
ENST00000525974.5:c.26G>T	ENSP00000434594.1:p.Gly9Val
ENST00000527284.5:c.224G>T	ENSP00000435312.1:p.Gly75Val
ENST00000527800.5:c.26G>T	ENSP00000433770.1:p.Gly9Val
ENST00000544898.5:c.317G>T	ENSP00000440898.2:p.Gly106Val
ENST00000545043.6:c.242G>T	ENSP00000438143.2:p.Gly81Val
ENST00000562484.2:c.26G>T	ENSP00000463326.1:p.Gly9Val
ENST00000563369.6:c.26G>T	ENSP00000463560.1:p.Gly9Val
ENST00000563478.5:c.26G>T	ENSP00000462341.1:p.Gly9Val
ENST00000564917.5:c.317G>T	ENSP00000455187.1:p.Gly106Val
ENST00000567357.5:c.*175G>T	ENSP00000457959.1:n.*175G>T
ENST00000569718.5:c.211G>T
ENST00000620035.4:c.263G>T	ENSP00000483833.1:p.Gly88Val
NM_001172643.1:c.224G>T	NP_001166114.1:p.Gly75Val
NM_001172644.1:c.242G>T	NP_001166115.1:p.Gly81Val
NM_001172645.1:c.263G>T	NP_001166116.1:p.Gly88Val
NM_001271934.1:c.170G>T	NP_001258863.1:p.Gly57Val
NM_001271935.1:c.224G>T	NP_001258864.1:p.Gly75Val
NM_001272050.1:c.26G>T	NP_001258979.1:p.Gly9Val
NM_004614.4:c.317G>T	NP_004605.4:p.Gly106Val
NR_073520.1:n.1596G>T
NM_001172644.2:c.242G>T	NP_001166115.1:p.Gly81Val
NM_001271934.2:c.170G>T	NP_001258863.1:p.Gly57Val
NM_001272050.2:c.26G>T	NP_001258979.1:p.Gly9Val
NM_004614.5:c.317G>T MANE Select	NP_004605.4:p.Gly106Val
NR_073520.2:n.1306G>T
NM_001172645.2:c.263G>T	NP_001166116.1:p.Gly88Val