Canonical Allele Identifier: CA2609446927

Gene: HK1

Linked Data

• gnomAD v4: 10-69382336-T-TCCGC

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69382336_69382337insCCGC , CM000672.2:g.69382336_69382337insCCGC	GRCh38
NC_000010.10:g.71142092_71142093insCCGC , CM000672.1:g.71142092_71142093insCCGC	GRCh37
NC_000010.9:g.70812098_70812099insCCGC	NCBI36
NG_012077.1:g.117337_117338insCCGC , LRG_365:g.117337_117338insCCGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470050.2:c.1266-151_1266-150insCCGC	ENSP00000515580.1:n.1266-151_1266-150insCCGC
ENST00000703945.1:c.1182-151_1182-150insCCGC	ENSP00000515578.1:n.1182-151_1182-150insCCGC
ENST00000703946.1:c.1265+2241_1265+2242insCCGC	ENSP00000515579.1:n.1265+2241_1265+2242insCCGC
ENST00000703947.1:c.876-151_876-150insCCGC	ENSP00000515581.1:n.876-151_876-150insCCGC
ENST00000703948.1:c.*883-151_*883-150insCCGC	ENSP00000515582.1:n.*883-151_*883-150insCCGC
ENST00000703949.1:c.1266-151_1266-150insCCGC	ENSP00000515583.1:n.1266-151_1266-150insCCGC
ENST00000703950.1:c.1266-151_1266-150insCCGC	ENSP00000515584.1:n.1266-151_1266-150insCCGC
ENST00000703951.1:c.1265+2241_1265+2242insCCGC	ENSP00000515585.1:n.1265+2241_1265+2242insCCGC
ENST00000703952.1:c.1265+2241_1265+2242insCCGC	ENSP00000515586.1:n.1265+2241_1265+2242insCCGC
ENST00000703953.1:c.*529-151_*529-150insCCGC	ENSP00000515587.1:n.*529-151_*529-150insCCGC
ENST00000703954.1:c.1146-151_1146-150insCCGC	ENSP00000515588.1:n.1146-151_1146-150insCCGC
ENST00000703955.1:n.1816-151_1816-150insCCGC
ENST00000298649.8:c.1263-151_1263-150insCCGC	ENSP00000298649.3:n.1263-151_1263-150insCCGC
ENST00000359426.7:c.1266-151_1266-150insCCGC MANE Select	ENSP00000352398.6:n.1266-151_1266-150insCCGC
ENST00000436817.6:c.1278-151_1278-150insCCGC	ENSP00000415949.2:n.1278-151_1278-150insCCGC
ENST00000493591.6:c.*1154-151_*1154-150insCCGC	ENSP00000494917.1:n.*1154-151_*1154-150insCCGC
ENST00000643399.2:c.1278-151_1278-150insCCGC MANE Plus Clinical	ENSP00000494664.1:n.1278-151_1278-150insCCGC
ENST00000298649.7:c.1263-151_1263-150insCCGC	ENSP00000298649.3:n.1263-151_1263-150insCCGC
ENST00000359426.6:c.1266-151_1266-150insCCGC	ENSP00000352398.6:n.1266-151_1266-150insCCGC
ENST00000360289.6:c.1230-151_1230-150insCCGC	ENSP00000353433.2:n.1230-151_1230-150insCCGC
ENST00000448642.6:c.1278-151_1278-150insCCGC	ENSP00000402103.3:n.1278-151_1278-150insCCGC
ENST00000494253.1:n.1492-151_1492-150insCCGC
NM_000188.2:c.1266-151_1266-150insCCGC	NP_000179.2:n.1266-151_1266-150insCCGC
NM_033496.2:c.1263-151_1263-150insCCGC	NP_277031.1:n.1263-151_1263-150insCCGC
NM_033497.2:c.1278-151_1278-150insCCGC	NP_277032.1:n.1278-151_1278-150insCCGC
NM_033498.2:c.1278-151_1278-150insCCGC	NP_277033.1:n.1278-151_1278-150insCCGC
NM_033500.2:c.1230-151_1230-150insCCGC , LRG_365t1:c.1230-151_1230-150insCCGC	NP_277035.2:n.1230-151_1230-150insCCGC
XM_005269735.2:c.1395-151_1395-150insCCGC	XP_005269792.1:n.1395-151_1395-150insCCGC
XM_005269736.1:c.1278-151_1278-150insCCGC	XP_005269793.1:n.1278-151_1278-150insCCGC
XM_005269737.1:c.1182-151_1182-150insCCGC	XP_005269794.1:n.1182-151_1182-150insCCGC
XM_011539732.1:c.1230-151_1230-150insCCGC	XP_011538034.1:n.1230-151_1230-150insCCGC
XM_011539733.1:c.1224-151_1224-150insCCGC	XP_011538035.1:n.1224-151_1224-150insCCGC
XM_011539734.1:c.1221-151_1221-150insCCGC	XP_011538036.1:n.1221-151_1221-150insCCGC
NM_001322364.1:c.1278-151_1278-150insCCGC	NP_001309293.1:n.1278-151_1278-150insCCGC
NM_001322365.1:c.1371-151_1371-150insCCGC	NP_001309294.1:n.1371-151_1371-150insCCGC
NM_001322366.1:c.1182-151_1182-150insCCGC	NP_001309295.1:n.1182-151_1182-150insCCGC
NM_001322367.1:c.1170-151_1170-150insCCGC	NP_001309296.1:n.1170-151_1170-150insCCGC
NM_001358263.1:c.1278-151_1278-150insCCGC MANE Plus Clinical	NP_001345192.1:n.1278-151_1278-150insCCGC
XM_024447969.1:c.1278-151_1278-150insCCGC	XP_024303737.1:n.1278-151_1278-150insCCGC
NM_000188.3:c.1266-151_1266-150insCCGC MANE Select	NP_000179.2:n.1266-151_1266-150insCCGC
NM_001322364.2:c.1278-151_1278-150insCCGC	NP_001309293.1:n.1278-151_1278-150insCCGC
NM_001322365.2:c.1371-151_1371-150insCCGC	NP_001309294.1:n.1371-151_1371-150insCCGC
NM_033496.3:c.1263-151_1263-150insCCGC	NP_277031.1:n.1263-151_1263-150insCCGC
NM_033497.3:c.1278-151_1278-150insCCGC	NP_277032.1:n.1278-151_1278-150insCCGC
NM_033498.3:c.1278-151_1278-150insCCGC	NP_277033.1:n.1278-151_1278-150insCCGC