Canonical Allele Identifier: CA1917772190

Gene: HK1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69382665_69382667delinsGAC , CM000672.2:g.69382665_69382667delinsGAC	GRCh38
NC_000010.10:g.71142421_71142423delinsGAC , CM000672.1:g.71142421_71142423delinsGAC	GRCh37
NC_000010.9:g.70812427_70812429delinsGAC	NCBI36
NG_012077.1:g.117666_117668delinsGAC , LRG_365:g.117666_117668delinsGAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470050.2:c.1444_1446delinsGAC	ENSP00000515580.1:p.Asp482=
ENST00000703945.1:c.1360_1362delinsGAC	ENSP00000515578.1:p.Asp454=
ENST00000703946.1:c.1265+2570_1265+2572delinsGAC	ENSP00000515579.1:n.1265+2570_1265+2572delinsGAC
ENST00000703947.1:c.1054_1056delinsGAC	ENSP00000515581.1:p.Asp352=
ENST00000703948.1:c.*1061_*1063delinsGAC	ENSP00000515582.1:n.*1061_*1063delinsGAC
ENST00000703949.1:c.1444_1446delinsGAC	ENSP00000515583.1:p.Asp482=
ENST00000703950.1:c.1444_1446delinsGAC	ENSP00000515584.1:p.Asp482=
ENST00000703951.1:c.1265+2570_1265+2572delinsGAC	ENSP00000515585.1:n.1265+2570_1265+2572delinsGAC
ENST00000703952.1:c.1265+2570_1265+2572delinsGAC	ENSP00000515586.1:n.1265+2570_1265+2572delinsGAC
ENST00000703953.1:c.*707_*709delinsGAC	ENSP00000515587.1:n.*707_*709delinsGAC
ENST00000703954.1:c.1324_1326delinsGAC	ENSP00000515588.1:p.Asp442=
ENST00000703955.1:n.1994_1996delinsGAC
ENST00000298649.8:c.1441_1443delinsGAC	ENSP00000298649.3:p.Asp481=
ENST00000359426.7:c.1444_1446delinsGAC MANE Select	ENSP00000352398.6:p.Asp482=
ENST00000436817.6:c.1456_1458delinsGAC	ENSP00000415949.2:p.Asp486=
ENST00000493591.6:c.*1332_*1334delinsGAC	ENSP00000494917.1:n.*1332_*1334delinsGAC
ENST00000643399.2:c.1456_1458delinsGAC MANE Plus Clinical	ENSP00000494664.1:p.Asp486=
ENST00000298649.7:c.1441_1443delinsGAC	ENSP00000298649.3:p.Asp481=
ENST00000359426.6:c.1444_1446delinsGAC	ENSP00000352398.6:p.Asp482=
ENST00000360289.6:c.1408_1410delinsGAC	ENSP00000353433.2:p.Asp470=
ENST00000448642.6:c.1456_1458delinsGAC	ENSP00000402103.3:p.Asp486=
ENST00000494253.1:n.1670_1672delinsGAC
NM_000188.2:c.1444_1446delinsGAC	NP_000179.2:p.Asp482=
NM_033496.2:c.1441_1443delinsGAC	NP_277031.1:p.Asp481=
NM_033497.2:c.1456_1458delinsGAC	NP_277032.1:p.Asp486=
NM_033498.2:c.1456_1458delinsGAC	NP_277033.1:p.Asp486=
NM_033500.2:c.1408_1410delinsGAC , LRG_365t1:c.1408_1410delinsGAC	NP_277035.2:p.Asp470=
XM_005269735.2:c.1573_1575delinsGAC	XP_005269792.1:p.Asp525=
XM_005269736.1:c.1456_1458delinsGAC	XP_005269793.1:p.Asp486=
XM_005269737.1:c.1360_1362delinsGAC	XP_005269794.1:p.Asp454=
XM_011539732.1:c.1408_1410delinsGAC	XP_011538034.1:p.Asp470=
XM_011539733.1:c.1402_1404delinsGAC	XP_011538035.1:p.Asp468=
XM_011539734.1:c.1399_1401delinsGAC	XP_011538036.1:p.Asp467=
NM_001322364.1:c.1456_1458delinsGAC	NP_001309293.1:p.Asp486=
NM_001322365.1:c.1549_1551delinsGAC	NP_001309294.1:p.Asp517=
NM_001322366.1:c.1360_1362delinsGAC	NP_001309295.1:p.Asp454=
NM_001322367.1:c.1348_1350delinsGAC	NP_001309296.1:p.Asp450=
NM_001358263.1:c.1456_1458delinsGAC MANE Plus Clinical	NP_001345192.1:p.Asp486=
XM_024447969.1:c.1456_1458delinsGAC	XP_024303737.1:p.Asp486=
NM_000188.3:c.1444_1446delinsGAC MANE Select	NP_000179.2:p.Asp482=
NM_001322364.2:c.1456_1458delinsGAC	NP_001309293.1:p.Asp486=
NM_001322365.2:c.1549_1551delinsGAC	NP_001309294.1:p.Asp517=
NM_033496.3:c.1441_1443delinsGAC	NP_277031.1:p.Asp481=
NM_033497.3:c.1456_1458delinsGAC	NP_277032.1:p.Asp486=
NM_033498.3:c.1456_1458delinsGAC	NP_277033.1:p.Asp486=