Canonical Allele Identifier: CA2579779818
Gene: TPK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.144648861_144648862delinsCG , CM000669.2:g.144648861_144648862delinsCG GRCh38
NC_000007.13:g.144345954_144345955delinsCG , CM000669.1:g.144345954_144345955delinsCG GRCh37
NC_000007.12:g.143976887_143976888delinsCG NCBI36
NG_032112.1:g.192192_192193delinsCG
NG_032112.2:g.192192_192193delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000639328.1:c.-116_-115delinsCG ENSP00000491869.1:n.-116_-115delinsCG
ENST00000360057.7:c.203_204delinsCG MANE Select ENSP00000353165.3:p.Ile68Thr
ENST00000378098.8:c.203_204delinsCG ENSP00000367338.4:p.Ile68Thr
ENST00000378099.7:c.203_204delinsCG ENSP00000367339.3:p.Ile68Thr
ENST00000481645.5:n.293_294delinsCG
ENST00000482940.5:c.*6_*7delinsCG ENSP00000449909.1:n.*6_*7delinsCG
ENST00000489798.5:c.67_68delinsCG ENSP00000450028.1:p.Ser23Arg
ENST00000538212.6:c.188_189delinsCG ENSP00000438813.2:p.Ile63Thr
ENST00000547966.5:n.101_102delinsCG
ENST00000551062.5:n.117_118delinsCG
ENST00000552881.1:c.203_204delinsCG ENSP00000448655.1:p.Ile68Thr
NM_001042482.1:c.203_204delinsCG NP_001035947.1:p.Ile68Thr
NM_022445.3:c.203_204delinsCG NP_071890.2:p.Ile68Thr
XM_005249970.1:c.203_204delinsCG XP_005250027.1:p.Ile68Thr
XM_006715925.2:c.-60-25601_-60-25600delinsCG XP_006715988.1:n.-60-25601_-60-25600delinsCG
XM_011516031.1:c.203_204delinsCG XP_011514333.1:p.Ile68Thr
XM_011516032.1:c.203_204delinsCG XP_011514334.1:p.Ile68Thr
XM_011516033.1:c.203_204delinsCG XP_011514335.1:p.Ile68Thr
XM_011516034.1:c.203_204delinsCG XP_011514336.1:p.Ile68Thr
XM_011516035.1:c.203_204delinsCG XP_011514337.1:p.Ile68Thr
XM_011516036.1:c.188_189delinsCG XP_011514338.1:p.Ile63Thr
XM_011516037.1:c.188_189delinsCG XP_011514339.1:p.Ile63Thr
XM_011516038.1:c.188_189delinsCG XP_011514340.1:p.Ile63Thr
XM_011516039.1:c.125_126delinsCG XP_011514341.1:p.Ile42Thr
XM_011516040.1:c.203_204delinsCG XP_011514342.1:p.Ile68Thr
XM_011516041.1:c.188_189delinsCG XP_011514343.1:p.Ile63Thr
XM_011516042.1:c.203_204delinsCG XP_011514344.1:p.Ile68Thr
XM_011516043.1:c.203_204delinsCG XP_011514345.1:p.Ile68Thr
XM_011516044.1:c.188_189delinsCG XP_011514346.1:p.Ile63Thr
XM_011516045.1:c.-251_-250delinsCG XP_011514347.1:n.-251_-250delinsCG
XM_011516046.1:c.203_204delinsCG XP_011514348.1:p.Ile68Thr
XM_011516047.1:c.-116_-115delinsCG XP_011514349.1:n.-116_-115delinsCG
XM_011516048.1:c.-116_-115delinsCG XP_011514350.1:n.-116_-115delinsCG
XM_011516049.1:c.-194_-193delinsCG XP_011514351.1:n.-194_-193delinsCG
XM_011516050.1:c.-194_-193delinsCG XP_011514352.1:n.-194_-193delinsCG
XR_927446.1:n.307_308delinsCG
XR_927448.1:n.307_308delinsCG
XR_927450.1:n.307_308delinsCG
XR_927451.1:n.307_308delinsCG
XR_927453.1:n.306_307delinsCG
NM_001350879.1:c.203_204delinsCG NP_001337808.1:p.Ile68Thr
NM_001350880.1:c.203_204delinsCG NP_001337809.1:p.Ile68Thr
NM_001350881.1:c.203_204delinsCG NP_001337810.1:p.Ile68Thr
NM_001350882.1:c.188_189delinsCG NP_001337811.1:p.Ile63Thr
NM_001350883.1:c.188_189delinsCG NP_001337812.1:p.Ile63Thr
NM_001350884.1:c.188_189delinsCG NP_001337813.1:p.Ile63Thr
NM_001350885.1:c.-116_-115delinsCG NP_001337814.1:n.-116_-115delinsCG
NM_001350886.1:c.-194_-193delinsCG NP_001337815.1:n.-194_-193delinsCG
NM_001350887.1:c.-60-25601_-60-25600delinsCG NP_001337816.1:n.-60-25601_-60-25600delinsCG
NM_001350889.1:c.-60-25601_-60-25600delinsCG NP_001337818.1:n.-60-25601_-60-25600delinsCG
NM_001350893.1:c.-116_-115delinsCG NP_001337822.1:n.-116_-115delinsCG
NM_001350894.1:c.-60-25601_-60-25600delinsCG NP_001337823.1:n.-60-25601_-60-25600delinsCG
NM_001350895.1:c.-271_-270delinsCG NP_001337824.1:n.-271_-270delinsCG
NR_146934.1:n.247_248delinsCG
NR_146935.1:n.386_387delinsCG
NR_146936.1:n.454_455delinsCG
XM_011516032.2:c.203_204delinsCG XP_011514334.1:p.Ile68Thr
XM_011516033.2:c.203_204delinsCG XP_011514335.1:p.Ile68Thr
XM_011516034.2:c.203_204delinsCG XP_011514336.1:p.Ile68Thr
XM_011516035.3:c.203_204delinsCG XP_011514337.1:p.Ile68Thr
XM_011516037.2:c.188_189delinsCG XP_011514339.1:p.Ile63Thr
XM_011516039.2:c.125_126delinsCG XP_011514341.1:p.Ile42Thr
XM_011516040.2:c.203_204delinsCG XP_011514342.1:p.Ile68Thr
XM_011516047.2:c.-116_-115delinsCG XP_011514349.1:n.-116_-115delinsCG
XM_017011969.1:c.203_204delinsCG XP_016867458.1:p.Ile68Thr
XM_017011970.1:c.188_189delinsCG XP_016867459.1:p.Ile63Thr
XM_017011971.1:c.188_189delinsCG XP_016867460.1:p.Ile63Thr
XM_017011972.1:c.203_204delinsCG XP_016867461.1:p.Ile68Thr
XM_017011974.1:c.125_126delinsCG XP_016867463.1:p.Ile42Thr
XM_017011975.1:c.125_126delinsCG XP_016867464.1:p.Ile42Thr
XM_017011982.1:c.-116_-115delinsCG XP_016867471.1:n.-116_-115delinsCG
XM_024446715.1:c.188_189delinsCG XP_024302483.1:p.Ile63Thr
XM_024446716.1:c.-271_-270delinsCG XP_024302484.1:n.-271_-270delinsCG
XM_024446717.1:c.-194_-193delinsCG XP_024302485.1:n.-194_-193delinsCG
XR_001744630.1:n.307_308delinsCG
NM_022445.4:c.203_204delinsCG MANE Select NP_071890.2:p.Ile68Thr
NM_001350884.2:c.188_189delinsCG NP_001337813.1:p.Ile63Thr
NR_146936.2:n.430_431delinsCG
NM_001042482.2:c.203_204delinsCG NP_001035947.1:p.Ile68Thr