Canonical Allele Identifier: CA623116073

Gene: TK2

Linked Data

• dbSNP Id: rs1355681110
• gnomAD v2: 16-66582920-AGAAAG-A
• gnomAD v4: 16-66549017-AGAAAG-A
• MyVariant Identifiers: chr16:g.66582921_66582925del (hg19) ; chr16:g.66549018_66549022del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66549022_66549026del , CM000678.2:g.66549022_66549026del	GRCh38
NC_000016.9:g.66582925_66582929del , CM000678.1:g.66582925_66582929del	GRCh37
NC_000016.8:g.65140426_65140430del	NCBI36
NG_016862.1:g.6391_6395del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299697.12:c.32-13_32-9del	ENSP00000299697.9:n.32-13_32-9del
ENST00000417693.8:c.125-13_125-9del	ENSP00000407469.5:n.125-13_125-9del
ENST00000451102.7:c.32-13_32-9del	ENSP00000414334.4:n.32-13_32-9del
ENST00000527284.6:c.69-13_69-9del
ENST00000527800.6:c.-180_-176del	ENSP00000433770.1:n.-180_-176del
ENST00000544898.6:c.125-13_125-9del MANE Select	ENSP00000440898.2:n.125-13_125-9del
ENST00000567357.6:c.125-13_125-9del	ENSP00000457959.2:n.125-13_125-9del
ENST00000569718.6:c.32-13_32-9del	ENSP00000464313.2:n.32-13_32-9del
ENST00000620035.5:c.125-13_125-9del	ENSP00000483833.2:n.125-13_125-9del
ENST00000677420.1:c.-126_-122del	ENSP00000504648.1:n.-126_-122del
ENST00000677555.1:c.-105_-101del	ENSP00000503331.1:n.-105_-101del
ENST00000677715.1:c.-167-13_-167-9del	ENSP00000502950.1:n.-167-13_-167-9del
ENST00000678015.1:c.-167-13_-167-9del	ENSP00000502959.1:n.-167-13_-167-9del
ENST00000678297.1:c.-92-13_-92-9del	ENSP00000503472.1:n.-92-13_-92-9del
ENST00000678314.1:c.-61+2518_-61+2522del	ENSP00000504438.1:n.-61+2518_-61+2522del
ENST00000679271.1:n.31-13_31-9del
ENST00000679327.1:n.1083_1087del
ENST00000299697.11:c.125-13_125-9del	ENSP00000299697.8:n.125-13_125-9del
ENST00000417693.7:c.251-13_251-9del	ENSP00000407469.4:n.251-13_251-9del
ENST00000451102.6:c.251-13_251-9del	ENSP00000414334.3:n.251-13_251-9del
ENST00000525974.5:c.-167-13_-167-9del	ENSP00000434594.1:n.-167-13_-167-9del
ENST00000527284.5:c.32-13_32-9del	ENSP00000435312.1:n.32-13_32-9del
ENST00000527800.5:c.-180_-176del	ENSP00000433770.1:n.-180_-176del
ENST00000544898.5:c.125-13_125-9del	ENSP00000440898.2:n.125-13_125-9del
ENST00000545043.6:c.125-13_125-9del	ENSP00000438143.2:n.125-13_125-9del
ENST00000562484.2:c.-167-13_-167-9del	ENSP00000463326.1:n.-167-13_-167-9del
ENST00000563369.6:c.-167-13_-167-9del	ENSP00000463560.1:n.-167-13_-167-9del
ENST00000563478.5:c.-167-13_-167-9del	ENSP00000462341.1:n.-167-13_-167-9del
ENST00000564917.5:c.125-13_125-9del	ENSP00000455187.1:n.125-13_125-9del
ENST00000567357.5:c.251-13_251-9del	ENSP00000457959.1:n.251-13_251-9del
ENST00000569718.5:c.19-13_19-9del
ENST00000620035.4:c.125-13_125-9del	ENSP00000483833.1:n.125-13_125-9del
NM_001172643.1:c.32-13_32-9del	NP_001166114.1:n.32-13_32-9del
NM_001172644.1:c.125-13_125-9del	NP_001166115.1:n.125-13_125-9del
NM_001172645.1:c.125-13_125-9del	NP_001166116.1:n.125-13_125-9del
NM_001271934.1:c.-118-13_-118-9del	NP_001258863.1:n.-118-13_-118-9del
NM_001271935.1:c.32-13_32-9del	NP_001258864.1:n.32-13_32-9del
NM_001272050.1:c.-167-13_-167-9del	NP_001258979.1:n.-167-13_-167-9del
NM_004614.4:c.125-13_125-9del	NP_004605.4:n.125-13_125-9del
NR_073520.1:n.1391_1395del
NM_001172644.2:c.125-13_125-9del	NP_001166115.1:n.125-13_125-9del
NM_001271934.2:c.-118-13_-118-9del	NP_001258863.1:n.-118-13_-118-9del
NM_001272050.2:c.-167-13_-167-9del	NP_001258979.1:n.-167-13_-167-9del
NM_004614.5:c.125-13_125-9del MANE Select	NP_004605.4:n.125-13_125-9del
NR_073520.2:n.1101_1105del
NM_001172645.2:c.125-13_125-9del	NP_001166116.1:n.125-13_125-9del