Canonical Allele Identifier: CA321998
Gene: TPK1 HGNC NCBI

Linked Data

ClinVar Variation Id: 215277
ClinVar RCV Id: RCV000197530
dbSNP Id: rs863224238

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.144623209del , CM000669.2:g.144623209del GRCh38
NC_000007.13:g.144320302del , CM000669.1:g.144320302del GRCh37
NC_000007.12:g.143951235del NCBI36
NG_032112.1:g.217845del
NG_032112.2:g.217845del

Transcript Alleles

HGVS Amino-acid change
ENST00000639328.1:c.-8del ENSP00000491869.1:n.-8del
ENST00000360057.7:c.311del MANE Select ENSP00000353165.3:p.Cys104SerfsTer9
ENST00000378098.8:c.311del ENSP00000367338.4:p.Cys104SerfsTer9
ENST00000378099.7:c.311del ENSP00000367339.3:p.Cys104SerfsTer9
ENST00000481645.5:n.401del
ENST00000482940.5:c.*114del ENSP00000449909.1:n.*114del
ENST00000538212.6:c.296del ENSP00000438813.2:p.Cys99SerfsTer9
ENST00000547966.5:n.209del
ENST00000548831.1:n.82del
ENST00000551062.5:n.225del
ENST00000552881.1:c.311del ENSP00000448655.1:p.Cys104SerfsTer9
NM_001042482.1:c.311del NP_001035947.1:p.Cys104SerfsTer9
NM_022445.3:c.311del NP_071890.2:p.Cys104SerfsTer9
XM_005249970.1:c.311del XP_005250027.1:p.Cys104SerfsTer9
XM_006715925.2:c.-8del XP_006715988.1:n.-8del
XM_011516031.1:c.389del XP_011514333.1:p.Cys130SerfsTer9
XM_011516032.1:c.389del XP_011514334.1:p.Cys130SerfsTer9
XM_011516033.1:c.389del XP_011514335.1:p.Cys130SerfsTer9
XM_011516034.1:c.389del XP_011514336.1:p.Cys130SerfsTer9
XM_011516035.1:c.389del XP_011514337.1:p.Cys130SerfsTer9
XM_011516036.1:c.374del XP_011514338.1:p.Cys125SerfsTer9
XM_011516037.1:c.374del XP_011514339.1:p.Cys125SerfsTer9
XM_011516038.1:c.374del XP_011514340.1:p.Cys125SerfsTer9
XM_011516039.1:c.311del XP_011514341.1:p.Cys104SerfsTer9
XM_011516040.1:c.389del XP_011514342.1:p.Cys130SerfsTer9
XM_011516041.1:c.296del XP_011514343.1:p.Cys99SerfsTer9
XM_011516042.1:c.389del XP_011514344.1:p.Cys130SerfsTer9
XM_011516043.1:c.389del XP_011514345.1:p.Cys130SerfsTer9
XM_011516044.1:c.296del XP_011514346.1:p.Cys99SerfsTer9
XM_011516045.1:c.71del XP_011514347.1:p.Cys24SerfsTer9
XM_011516046.1:c.389del XP_011514348.1:p.Cys130SerfsTer9
XM_011516047.1:c.-8del XP_011514349.1:n.-8del
XM_011516048.1:c.-8del XP_011514350.1:n.-8del
XM_011516049.1:c.-8del XP_011514351.1:n.-8del
XM_011516050.1:c.-8del XP_011514352.1:n.-8del
XR_927446.1:n.493del
XR_927448.1:n.493del
XR_927450.1:n.493del
XR_927451.1:n.493del
XR_927453.1:n.414del
NM_001350879.1:c.311del NP_001337808.1:p.Cys104SerfsTer9
NM_001350880.1:c.311del NP_001337809.1:p.Cys104SerfsTer9
NM_001350881.1:c.311del NP_001337810.1:p.Cys104SerfsTer9
NM_001350882.1:c.296del NP_001337811.1:p.Cys99SerfsTer9
NM_001350883.1:c.296del NP_001337812.1:p.Cys99SerfsTer9
NM_001350884.1:c.296del NP_001337813.1:p.Cys99SerfsTer9
NM_001350885.1:c.-8del NP_001337814.1:n.-8del
NM_001350886.1:c.-8del NP_001337815.1:n.-8del
NM_001350887.1:c.-8del NP_001337816.1:n.-8del
NM_001350889.1:c.-8del NP_001337818.1:n.-8del
NM_001350893.1:c.-8del NP_001337822.1:n.-8del
NM_001350894.1:c.-8del NP_001337823.1:n.-8del
NM_001350895.1:c.-163del NP_001337824.1:n.-163del
NR_146934.1:n.355del
NR_146935.1:n.494del
NR_146936.1:n.562del
XM_011516032.2:c.389del XP_011514334.1:p.Cys130SerfsTer9
XM_011516033.2:c.389del XP_011514335.1:p.Cys130SerfsTer9
XM_011516034.2:c.389del XP_011514336.1:p.Cys130SerfsTer9
XM_011516035.3:c.389del XP_011514337.1:p.Cys130SerfsTer9
XM_011516037.2:c.374del XP_011514339.1:p.Cys125SerfsTer9
XM_011516039.2:c.311del XP_011514341.1:p.Cys104SerfsTer9
XM_011516040.2:c.389del XP_011514342.1:p.Cys130SerfsTer9
XM_011516047.2:c.-8del XP_011514349.1:n.-8del
XM_017011969.1:c.389del XP_016867458.1:p.Cys130SerfsTer9
XM_017011970.1:c.374del XP_016867459.1:p.Cys125SerfsTer9
XM_017011971.1:c.374del XP_016867460.1:p.Cys125SerfsTer9
XM_017011972.1:c.389del XP_016867461.1:p.Cys130SerfsTer9
XM_017011974.1:c.311del XP_016867463.1:p.Cys104SerfsTer9
XM_017011975.1:c.311del XP_016867464.1:p.Cys104SerfsTer9
XM_017011980.2:c.71del XP_016867469.1:p.Cys24SerfsTer9
XM_017011981.2:c.71del XP_016867470.1:p.Cys24SerfsTer9
XM_017011982.1:c.-8del XP_016867471.1:n.-8del
XM_024446715.1:c.296del XP_024302483.1:p.Cys99SerfsTer9
XM_024446716.1:c.-163del XP_024302484.1:n.-163del
XM_024446717.1:c.-8del XP_024302485.1:n.-8del
XR_001744630.1:n.493del
NM_022445.4:c.311del MANE Select NP_071890.2:p.Cys104SerfsTer9
NM_001350884.2:c.296del NP_001337813.1:p.Cys99SerfsTer9
NR_146936.2:n.538del
NM_001042482.2:c.311del NP_001035947.1:p.Cys104SerfsTer9