Canonical Allele Identifier: CA2579781157

Gene: TPK1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.144453620_144453621delinsGC , CM000669.2:g.144453620_144453621delinsGC	GRCh38
NC_000007.13:g.144150713_144150714delinsGC , CM000669.1:g.144150713_144150714delinsGC	GRCh37
NC_000007.12:g.143781646_143781647delinsGC	NCBI36
NG_032112.1:g.387433_387434delinsGC
NG_032112.2:g.387433_387434delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360057.7:c.656_657delinsGC MANE Select	ENSP00000353165.3:p.Asn219Ser
ENST00000378098.8:c.*412_*413delinsGC	ENSP00000367338.4:n.*412_*413delinsGC
ENST00000378099.7:c.509_510delinsGC	ENSP00000367339.3:p.Asn170Ser
ENST00000482940.5:c.*687_*688delinsGC	ENSP00000449909.1:n.*687_*688delinsGC
ENST00000538212.6:c.494_495delinsGC	ENSP00000438813.2:p.Asn165Ser
ENST00000547966.5:n.554_555delinsGC
NM_001042482.1:c.509_510delinsGC	NP_001035947.1:p.Asn170Ser
NM_022445.3:c.656_657delinsGC	NP_071890.2:p.Asn219Ser
XM_005249970.1:c.656_657delinsGC	XP_005250027.1:p.Asn219Ser
XM_006715925.2:c.338_339delinsGC	XP_006715988.1:p.Asn113Ser
XM_011516031.1:c.734_735delinsGC	XP_011514333.1:p.Asn245Ser
XM_011516032.1:c.734_735delinsGC	XP_011514334.1:p.Asn245Ser
XM_011516033.1:c.734_735delinsGC	XP_011514335.1:p.Asn245Ser
XM_011516034.1:c.734_735delinsGC	XP_011514336.1:p.Asn245Ser
XM_011516035.1:c.*36_*37delinsGC	XP_011514337.1:n.*36_*37delinsGC
XM_011516036.1:c.719_720delinsGC	XP_011514338.1:p.Asn240Ser
XM_011516037.1:c.719_720delinsGC	XP_011514339.1:p.Asn240Ser
XM_011516038.1:c.719_720delinsGC	XP_011514340.1:p.Asn240Ser
XM_011516039.1:c.656_657delinsGC	XP_011514341.1:p.Asn219Ser
XM_011516041.1:c.641_642delinsGC	XP_011514343.1:p.Asn214Ser
XM_011516043.1:c.587_588delinsGC	XP_011514345.1:p.Asn196Ser
XM_011516044.1:c.494_495delinsGC	XP_011514346.1:p.Asn165Ser
XM_011516045.1:c.416_417delinsGC	XP_011514347.1:p.Asn139Ser
XM_011516047.1:c.338_339delinsGC	XP_011514349.1:p.Asn113Ser
XM_011516048.1:c.338_339delinsGC	XP_011514350.1:p.Asn113Ser
XM_011516049.1:c.338_339delinsGC	XP_011514351.1:p.Asn113Ser
XM_011516050.1:c.338_339delinsGC	XP_011514352.1:p.Asn113Ser
XR_927446.1:n.1183_1184delinsGC
XR_927448.1:n.1077_1078delinsGC
XR_927453.1:n.881_882delinsGC
NM_001350879.1:c.656_657delinsGC	NP_001337808.1:p.Asn219Ser
NM_001350880.1:c.509_510delinsGC	NP_001337809.1:p.Asn170Ser
NM_001350881.1:c.*36_*37delinsGC	NP_001337810.1:n.*36_*37delinsGC
NM_001350882.1:c.641_642delinsGC	NP_001337811.1:p.Asn214Ser
NM_001350883.1:c.641_642delinsGC	NP_001337812.1:p.Asn214Ser
NM_001350884.1:c.641_642delinsGC	NP_001337813.1:p.Asn214Ser
NM_001350885.1:c.338_339delinsGC	NP_001337814.1:p.Asn113Ser
NM_001350886.1:c.338_339delinsGC	NP_001337815.1:p.Asn113Ser
NM_001350887.1:c.338_339delinsGC	NP_001337816.1:p.Asn113Ser
NM_001350889.1:c.338_339delinsGC	NP_001337818.1:p.Asn113Ser
NM_001350893.1:c.338_339delinsGC	NP_001337822.1:p.Asn113Ser
NM_001350894.1:c.338_339delinsGC	NP_001337823.1:p.Asn113Ser
NM_001350895.1:c.305_306delinsGC	NP_001337824.1:p.Asn102Ser
NR_146934.1:n.553_554delinsGC
NR_146935.1:n.692_693delinsGC
NR_146936.1:n.1135_1136delinsGC
XM_011516032.2:c.734_735delinsGC	XP_011514334.1:p.Asn245Ser
XM_011516033.2:c.734_735delinsGC	XP_011514335.1:p.Asn245Ser
XM_011516034.2:c.734_735delinsGC	XP_011514336.1:p.Asn245Ser
XM_011516035.3:c.*36_*37delinsGC	XP_011514337.1:n.*36_*37delinsGC
XM_011516037.2:c.719_720delinsGC	XP_011514339.1:p.Asn240Ser
XM_011516039.2:c.656_657delinsGC	XP_011514341.1:p.Asn219Ser
XM_011516047.2:c.338_339delinsGC	XP_011514349.1:p.Asn113Ser
XM_017011970.1:c.719_720delinsGC	XP_016867459.1:p.Asn240Ser
XM_017011971.1:c.719_720delinsGC	XP_016867460.1:p.Asn240Ser
XM_017011974.1:c.656_657delinsGC	XP_016867463.1:p.Asn219Ser
XM_017011975.1:c.656_657delinsGC	XP_016867464.1:p.Asn219Ser
XM_017011980.2:c.416_417delinsGC	XP_016867469.1:p.Asn139Ser
XM_017011981.2:c.416_417delinsGC	XP_016867470.1:p.Asn139Ser
XM_017011982.1:c.338_339delinsGC	XP_016867471.1:p.Asn113Ser
XM_024446715.1:c.494_495delinsGC	XP_024302483.1:p.Asn165Ser
XM_024446716.1:c.305_306delinsGC	XP_024302484.1:p.Asn102Ser
XM_024446717.1:c.338_339delinsGC	XP_024302485.1:p.Asn113Ser
NM_022445.4:c.656_657delinsGC MANE Select	NP_071890.2:p.Asn219Ser
NM_001350884.2:c.641_642delinsGC	NP_001337813.1:p.Asn214Ser
NR_146936.2:n.1111_1112delinsGC
NM_001042482.2:c.509_510delinsGC	NP_001035947.1:p.Asn170Ser