Canonical Allele Identifier: CA2609446976

Gene: HK1

Linked Data

• gnomAD v4: 10-69382394-AAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69382397_69382398del , CM000672.2:g.69382397_69382398del	GRCh38
NC_000010.10:g.71142153_71142154del , CM000672.1:g.71142153_71142154del	GRCh37
NC_000010.9:g.70812159_70812160del	NCBI36
NG_012077.1:g.117398_117399del , LRG_365:g.117398_117399del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470050.2:c.1266-90_1266-89del	ENSP00000515580.1:n.1266-90_1266-89del
ENST00000703945.1:c.1182-90_1182-89del	ENSP00000515578.1:n.1182-90_1182-89del
ENST00000703946.1:c.1265+2302_1265+2303del	ENSP00000515579.1:n.1265+2302_1265+2303del
ENST00000703947.1:c.876-90_876-89del	ENSP00000515581.1:n.876-90_876-89del
ENST00000703948.1:c.*883-90_*883-89del	ENSP00000515582.1:n.*883-90_*883-89del
ENST00000703949.1:c.1266-90_1266-89del	ENSP00000515583.1:n.1266-90_1266-89del
ENST00000703950.1:c.1266-90_1266-89del	ENSP00000515584.1:n.1266-90_1266-89del
ENST00000703951.1:c.1265+2302_1265+2303del	ENSP00000515585.1:n.1265+2302_1265+2303del
ENST00000703952.1:c.1265+2302_1265+2303del	ENSP00000515586.1:n.1265+2302_1265+2303del
ENST00000703953.1:c.*529-90_*529-89del	ENSP00000515587.1:n.*529-90_*529-89del
ENST00000703954.1:c.1146-90_1146-89del	ENSP00000515588.1:n.1146-90_1146-89del
ENST00000703955.1:n.1816-90_1816-89del
ENST00000298649.8:c.1263-90_1263-89del	ENSP00000298649.3:n.1263-90_1263-89del
ENST00000359426.7:c.1266-90_1266-89del MANE Select	ENSP00000352398.6:n.1266-90_1266-89del
ENST00000436817.6:c.1278-90_1278-89del	ENSP00000415949.2:n.1278-90_1278-89del
ENST00000493591.6:c.*1154-90_*1154-89del	ENSP00000494917.1:n.*1154-90_*1154-89del
ENST00000643399.2:c.1278-90_1278-89del MANE Plus Clinical	ENSP00000494664.1:n.1278-90_1278-89del
ENST00000298649.7:c.1263-90_1263-89del	ENSP00000298649.3:n.1263-90_1263-89del
ENST00000359426.6:c.1266-90_1266-89del	ENSP00000352398.6:n.1266-90_1266-89del
ENST00000360289.6:c.1230-90_1230-89del	ENSP00000353433.2:n.1230-90_1230-89del
ENST00000448642.6:c.1278-90_1278-89del	ENSP00000402103.3:n.1278-90_1278-89del
ENST00000494253.1:n.1492-90_1492-89del
NM_000188.2:c.1266-90_1266-89del	NP_000179.2:n.1266-90_1266-89del
NM_033496.2:c.1263-90_1263-89del	NP_277031.1:n.1263-90_1263-89del
NM_033497.2:c.1278-90_1278-89del	NP_277032.1:n.1278-90_1278-89del
NM_033498.2:c.1278-90_1278-89del	NP_277033.1:n.1278-90_1278-89del
NM_033500.2:c.1230-90_1230-89del , LRG_365t1:c.1230-90_1230-89del	NP_277035.2:n.1230-90_1230-89del
XM_005269735.2:c.1395-90_1395-89del	XP_005269792.1:n.1395-90_1395-89del
XM_005269736.1:c.1278-90_1278-89del	XP_005269793.1:n.1278-90_1278-89del
XM_005269737.1:c.1182-90_1182-89del	XP_005269794.1:n.1182-90_1182-89del
XM_011539732.1:c.1230-90_1230-89del	XP_011538034.1:n.1230-90_1230-89del
XM_011539733.1:c.1224-90_1224-89del	XP_011538035.1:n.1224-90_1224-89del
XM_011539734.1:c.1221-90_1221-89del	XP_011538036.1:n.1221-90_1221-89del
NM_001322364.1:c.1278-90_1278-89del	NP_001309293.1:n.1278-90_1278-89del
NM_001322365.1:c.1371-90_1371-89del	NP_001309294.1:n.1371-90_1371-89del
NM_001322366.1:c.1182-90_1182-89del	NP_001309295.1:n.1182-90_1182-89del
NM_001322367.1:c.1170-90_1170-89del	NP_001309296.1:n.1170-90_1170-89del
NM_001358263.1:c.1278-90_1278-89del MANE Plus Clinical	NP_001345192.1:n.1278-90_1278-89del
XM_024447969.1:c.1278-90_1278-89del	XP_024303737.1:n.1278-90_1278-89del
NM_000188.3:c.1266-90_1266-89del MANE Select	NP_000179.2:n.1266-90_1266-89del
NM_001322364.2:c.1278-90_1278-89del	NP_001309293.1:n.1278-90_1278-89del
NM_001322365.2:c.1371-90_1371-89del	NP_001309294.1:n.1371-90_1371-89del
NM_033496.3:c.1263-90_1263-89del	NP_277031.1:n.1263-90_1263-89del
NM_033497.3:c.1278-90_1278-89del	NP_277032.1:n.1278-90_1278-89del
NM_033498.3:c.1278-90_1278-89del	NP_277033.1:n.1278-90_1278-89del