Canonical Allele Identifier: CA1917771565
Gene: HK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.69382027_69382029delinsCCT , CM000672.2:g.69382027_69382029delinsCCT GRCh38
NC_000010.10:g.71141783_71141785delinsCCT , CM000672.1:g.71141783_71141785delinsCCT GRCh37
NC_000010.9:g.70811789_70811791delinsCCT NCBI36
NG_012077.1:g.117028_117030delinsCCT , LRG_365:g.117028_117030delinsCCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000470050.2:c.1266-460_1266-458delinsCCT ENSP00000515580.1:n.1266-460_1266-458delinsCCT
ENST00000703945.1:c.1182-460_1182-458delinsCCT ENSP00000515578.1:n.1182-460_1182-458delinsCCT
ENST00000703946.1:c.1265+1932_1265+1934delinsCCT ENSP00000515579.1:n.1265+1932_1265+1934delinsCCT
ENST00000703947.1:c.876-460_876-458delinsCCT ENSP00000515581.1:n.876-460_876-458delinsCCT
ENST00000703948.1:c.*883-460_*883-458delinsCCT ENSP00000515582.1:n.*883-460_*883-458delinsCCT
ENST00000703949.1:c.1266-460_1266-458delinsCCT ENSP00000515583.1:n.1266-460_1266-458delinsCCT
ENST00000703950.1:c.1266-460_1266-458delinsCCT ENSP00000515584.1:n.1266-460_1266-458delinsCCT
ENST00000703951.1:c.1265+1932_1265+1934delinsCCT ENSP00000515585.1:n.1265+1932_1265+1934delinsCCT
ENST00000703952.1:c.1265+1932_1265+1934delinsCCT ENSP00000515586.1:n.1265+1932_1265+1934delinsCCT
ENST00000703953.1:c.*529-460_*529-458delinsCCT ENSP00000515587.1:n.*529-460_*529-458delinsCCT
ENST00000703954.1:c.1146-460_1146-458delinsCCT ENSP00000515588.1:n.1146-460_1146-458delinsCCT
ENST00000703955.1:n.1816-460_1816-458delinsCCT
ENST00000298649.8:c.1263-460_1263-458delinsCCT ENSP00000298649.3:n.1263-460_1263-458delinsCCT
ENST00000359426.7:c.1266-460_1266-458delinsCCT MANE Select ENSP00000352398.6:n.1266-460_1266-458delinsCCT
ENST00000436817.6:c.1278-460_1278-458delinsCCT ENSP00000415949.2:n.1278-460_1278-458delinsCCT
ENST00000493591.6:c.*1154-460_*1154-458delinsCCT ENSP00000494917.1:n.*1154-460_*1154-458delinsCCT
ENST00000643399.2:c.1278-460_1278-458delinsCCT MANE Plus Clinical ENSP00000494664.1:n.1278-460_1278-458delinsCCT
ENST00000298649.7:c.1263-460_1263-458delinsCCT ENSP00000298649.3:n.1263-460_1263-458delinsCCT
ENST00000359426.6:c.1266-460_1266-458delinsCCT ENSP00000352398.6:n.1266-460_1266-458delinsCCT
ENST00000360289.6:c.1230-460_1230-458delinsCCT ENSP00000353433.2:n.1230-460_1230-458delinsCCT
ENST00000448642.6:c.1278-460_1278-458delinsCCT ENSP00000402103.3:n.1278-460_1278-458delinsCCT
ENST00000494253.1:n.1492-460_1492-458delinsCCT
NM_000188.2:c.1266-460_1266-458delinsCCT NP_000179.2:n.1266-460_1266-458delinsCCT
NM_033496.2:c.1263-460_1263-458delinsCCT NP_277031.1:n.1263-460_1263-458delinsCCT
NM_033497.2:c.1278-460_1278-458delinsCCT NP_277032.1:n.1278-460_1278-458delinsCCT
NM_033498.2:c.1278-460_1278-458delinsCCT NP_277033.1:n.1278-460_1278-458delinsCCT
NM_033500.2:c.1230-460_1230-458delinsCCT , LRG_365t1:c.1230-460_1230-458delinsCCT NP_277035.2:n.1230-460_1230-458delinsCCT
XM_005269735.2:c.1395-460_1395-458delinsCCT XP_005269792.1:n.1395-460_1395-458delinsCCT
XM_005269736.1:c.1278-460_1278-458delinsCCT XP_005269793.1:n.1278-460_1278-458delinsCCT
XM_005269737.1:c.1182-460_1182-458delinsCCT XP_005269794.1:n.1182-460_1182-458delinsCCT
XM_011539732.1:c.1230-460_1230-458delinsCCT XP_011538034.1:n.1230-460_1230-458delinsCCT
XM_011539733.1:c.1224-460_1224-458delinsCCT XP_011538035.1:n.1224-460_1224-458delinsCCT
XM_011539734.1:c.1221-460_1221-458delinsCCT XP_011538036.1:n.1221-460_1221-458delinsCCT
NM_001322364.1:c.1278-460_1278-458delinsCCT NP_001309293.1:n.1278-460_1278-458delinsCCT
NM_001322365.1:c.1371-460_1371-458delinsCCT NP_001309294.1:n.1371-460_1371-458delinsCCT
NM_001322366.1:c.1182-460_1182-458delinsCCT NP_001309295.1:n.1182-460_1182-458delinsCCT
NM_001322367.1:c.1170-460_1170-458delinsCCT NP_001309296.1:n.1170-460_1170-458delinsCCT
NM_001358263.1:c.1278-460_1278-458delinsCCT MANE Plus Clinical NP_001345192.1:n.1278-460_1278-458delinsCCT
XM_024447969.1:c.1278-460_1278-458delinsCCT XP_024303737.1:n.1278-460_1278-458delinsCCT
NM_000188.3:c.1266-460_1266-458delinsCCT MANE Select NP_000179.2:n.1266-460_1266-458delinsCCT
NM_001322364.2:c.1278-460_1278-458delinsCCT NP_001309293.1:n.1278-460_1278-458delinsCCT
NM_001322365.2:c.1371-460_1371-458delinsCCT NP_001309294.1:n.1371-460_1371-458delinsCCT
NM_033496.3:c.1263-460_1263-458delinsCCT NP_277031.1:n.1263-460_1263-458delinsCCT
NM_033497.3:c.1278-460_1278-458delinsCCT NP_277032.1:n.1278-460_1278-458delinsCCT
NM_033498.3:c.1278-460_1278-458delinsCCT NP_277033.1:n.1278-460_1278-458delinsCCT