Canonical Allele Identifier: CA667919755

Gene: HK1

Linked Data

• dbSNP Id: rs1284563147
• gnomAD v3: 10-69382400-TAA-T
• gnomAD v4: 10-69382400-TAA-T
• MyVariant Identifiers: chr10:g.71142157_71142158del (hg19) ; chr10:g.69382401_69382402del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69382402_69382403del , CM000672.2:g.69382402_69382403del	GRCh38
NC_000010.10:g.71142158_71142159del , CM000672.1:g.71142158_71142159del	GRCh37
NC_000010.9:g.70812164_70812165del	NCBI36
NG_012077.1:g.117403_117404del , LRG_365:g.117403_117404del

Transcript Alleles

HGVS	Amino-acid change
ENST00000470050.2:c.1266-85_1266-84del	ENSP00000515580.1:n.1266-85_1266-84del
ENST00000703945.1:c.1182-85_1182-84del	ENSP00000515578.1:n.1182-85_1182-84del
ENST00000703946.1:c.1265+2307_1265+2308del	ENSP00000515579.1:n.1265+2307_1265+2308de...
ENST00000703947.1:c.876-85_876-84del	ENSP00000515581.1:n.876-85_876-84del
ENST00000703948.1:c.*883-85_*883-84del	ENSP00000515582.1:n.*883-85_*883-84del
ENST00000703949.1:c.1266-85_1266-84del	ENSP00000515583.1:n.1266-85_1266-84del
ENST00000703950.1:c.1266-85_1266-84del	ENSP00000515584.1:n.1266-85_1266-84del
ENST00000703951.1:c.1265+2307_1265+2308del	ENSP00000515585.1:n.1265+2307_1265+2308de...
ENST00000703952.1:c.1265+2307_1265+2308del	ENSP00000515586.1:n.1265+2307_1265+2308de...
ENST00000703953.1:c.*529-85_*529-84del	ENSP00000515587.1:n.*529-85_*529-84del
ENST00000703954.1:c.1146-85_1146-84del	ENSP00000515588.1:n.1146-85_1146-84del
ENST00000703955.1:n.1816-85_1816-84del
ENST00000298649.8:c.1263-85_1263-84del	ENSP00000298649.3:n.1263-85_1263-84del
ENST00000359426.7:c.1266-85_1266-84del MANE Select	ENSP00000352398.6:n.1266-85_1266-84del
ENST00000436817.6:c.1278-85_1278-84del	ENSP00000415949.2:n.1278-85_1278-84del
ENST00000493591.6:c.*1154-85_*1154-84del	ENSP00000494917.1:n.*1154-85_*1154-84del
ENST00000643399.2:c.1278-85_1278-84del MANE Plus Clinical	ENSP00000494664.1:n.1278-85_1278-84del
ENST00000298649.7:c.1263-85_1263-84del	ENSP00000298649.3:n.1263-85_1263-84del
ENST00000359426.6:c.1266-85_1266-84del	ENSP00000352398.6:n.1266-85_1266-84del
ENST00000360289.6:c.1230-85_1230-84del	ENSP00000353433.2:n.1230-85_1230-84del
ENST00000448642.6:c.1278-85_1278-84del	ENSP00000402103.3:n.1278-85_1278-84del
ENST00000494253.1:n.1492-85_1492-84del
NM_000188.2:c.1266-85_1266-84del	NP_000179.2:n.1266-85_1266-84del
NM_033496.2:c.1263-85_1263-84del	NP_277031.1:n.1263-85_1263-84del
NM_033497.2:c.1278-85_1278-84del	NP_277032.1:n.1278-85_1278-84del
NM_033498.2:c.1278-85_1278-84del	NP_277033.1:n.1278-85_1278-84del
NM_033500.2:c.1230-85_1230-84del , LRG_365t1:c.1230-85_1230-84del	NP_277035.2:n.1230-85_1230-84del
XM_005269735.2:c.1395-85_1395-84del	XP_005269792.1:n.1395-85_1395-84del
XM_005269736.1:c.1278-85_1278-84del	XP_005269793.1:n.1278-85_1278-84del
XM_005269737.1:c.1182-85_1182-84del	XP_005269794.1:n.1182-85_1182-84del
XM_011539732.1:c.1230-85_1230-84del	XP_011538034.1:n.1230-85_1230-84del
XM_011539733.1:c.1224-85_1224-84del	XP_011538035.1:n.1224-85_1224-84del
XM_011539734.1:c.1221-85_1221-84del	XP_011538036.1:n.1221-85_1221-84del
NM_001322364.1:c.1278-85_1278-84del	NP_001309293.1:n.1278-85_1278-84del
NM_001322365.1:c.1371-85_1371-84del	NP_001309294.1:n.1371-85_1371-84del
NM_001322366.1:c.1182-85_1182-84del	NP_001309295.1:n.1182-85_1182-84del
NM_001322367.1:c.1170-85_1170-84del	NP_001309296.1:n.1170-85_1170-84del
NM_001358263.1:c.1278-85_1278-84del MANE Plus Clinical	NP_001345192.1:n.1278-85_1278-84del
XM_024447969.1:c.1278-85_1278-84del	XP_024303737.1:n.1278-85_1278-84del
NM_000188.3:c.1266-85_1266-84del MANE Select	NP_000179.2:n.1266-85_1266-84del
NM_001322364.2:c.1278-85_1278-84del	NP_001309293.1:n.1278-85_1278-84del
NM_001322365.2:c.1371-85_1371-84del	NP_001309294.1:n.1371-85_1371-84del
NM_033496.3:c.1263-85_1263-84del	NP_277031.1:n.1263-85_1263-84del
NM_033497.3:c.1278-85_1278-84del	NP_277032.1:n.1278-85_1278-84del
NM_033498.3:c.1278-85_1278-84del	NP_277033.1:n.1278-85_1278-84del