Canonical Allele Identifier: CA2501531503
Gene: HK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.69384179_69384180del , CM000672.2:g.69384179_69384180del GRCh38
NC_000010.10:g.71143935_71143936del , CM000672.1:g.71143935_71143936del GRCh37
NC_000010.9:g.70813941_70813942del NCBI36
NG_012077.1:g.119180_119181del , LRG_365:g.119180_119181del

Transcript Alleles

HGVS Amino-acid Change
ENST00000470050.2:c.1571-154_1571-153del ENSP00000515580.1:n.1571-154_1571-153del
ENST00000703945.1:c.1487-154_1487-153del ENSP00000515578.1:n.1487-154_1487-153del
ENST00000703946.1:c.1265+4084_1265+4085del ENSP00000515579.1:n.1265+4084_1265+4085del
ENST00000703947.1:c.1181-154_1181-153del ENSP00000515581.1:n.1181-154_1181-153del
ENST00000703948.1:c.*1188-154_*1188-153del ENSP00000515582.1:n.*1188-154_*1188-153del
ENST00000703949.1:c.1571-154_1571-153del ENSP00000515583.1:n.1571-154_1571-153del
ENST00000703950.1:c.1571-154_1571-153del ENSP00000515584.1:n.1571-154_1571-153del
ENST00000703951.1:c.1265+4084_1265+4085del ENSP00000515585.1:n.1265+4084_1265+4085del
ENST00000703952.1:c.1265+4084_1265+4085del ENSP00000515586.1:n.1265+4084_1265+4085del
ENST00000703953.1:c.*834-154_*834-153del ENSP00000515587.1:n.*834-154_*834-153del
ENST00000703954.1:c.1451-154_1451-153del ENSP00000515588.1:n.1451-154_1451-153del
ENST00000703955.1:n.2121-154_2121-153del
ENST00000703957.1:n.76-154_76-153del
ENST00000298649.8:c.1568-154_1568-153del ENSP00000298649.3:n.1568-154_1568-153del
ENST00000359426.7:c.1571-154_1571-153del MANE Select ENSP00000352398.6:n.1571-154_1571-153del
ENST00000436817.6:c.1583-154_1583-153del ENSP00000415949.2:n.1583-154_1583-153del
ENST00000493591.6:c.*1459-154_*1459-153del ENSP00000494917.1:n.*1459-154_*1459-153del
ENST00000643399.2:c.1583-154_1583-153del MANE Plus Clinical ENSP00000494664.1:n.1583-154_1583-153del
ENST00000298649.7:c.1568-154_1568-153del ENSP00000298649.3:n.1568-154_1568-153del
ENST00000359426.6:c.1571-154_1571-153del ENSP00000352398.6:n.1571-154_1571-153del
ENST00000360289.6:c.1535-154_1535-153del ENSP00000353433.2:n.1535-154_1535-153del
ENST00000448642.6:c.1583-154_1583-153del ENSP00000402103.3:n.1583-154_1583-153del
ENST00000494253.1:n.1797-154_1797-153del
NM_000188.2:c.1571-154_1571-153del NP_000179.2:n.1571-154_1571-153del
NM_033496.2:c.1568-154_1568-153del NP_277031.1:n.1568-154_1568-153del
NM_033497.2:c.1583-154_1583-153del NP_277032.1:n.1583-154_1583-153del
NM_033498.2:c.1583-154_1583-153del NP_277033.1:n.1583-154_1583-153del
NM_033500.2:c.1535-154_1535-153del , LRG_365t1:c.1535-154_1535-153del NP_277035.2:n.1535-154_1535-153del
XM_005269735.2:c.1700-154_1700-153del XP_005269792.1:n.1700-154_1700-153del
XM_005269736.1:c.1583-154_1583-153del XP_005269793.1:n.1583-154_1583-153del
XM_005269737.1:c.1487-154_1487-153del XP_005269794.1:n.1487-154_1487-153del
XM_011539732.1:c.1535-154_1535-153del XP_011538034.1:n.1535-154_1535-153del
XM_011539733.1:c.1529-154_1529-153del XP_011538035.1:n.1529-154_1529-153del
XM_011539734.1:c.1526-154_1526-153del XP_011538036.1:n.1526-154_1526-153del
NM_001322364.1:c.1583-154_1583-153del NP_001309293.1:n.1583-154_1583-153del
NM_001322365.1:c.1676-154_1676-153del NP_001309294.1:n.1676-154_1676-153del
NM_001322366.1:c.1487-154_1487-153del NP_001309295.1:n.1487-154_1487-153del
NM_001322367.1:c.1475-154_1475-153del NP_001309296.1:n.1475-154_1475-153del
NM_001358263.1:c.1583-154_1583-153del MANE Plus Clinical NP_001345192.1:n.1583-154_1583-153del
XM_024447969.1:c.1583-154_1583-153del XP_024303737.1:n.1583-154_1583-153del
NM_000188.3:c.1571-154_1571-153del MANE Select NP_000179.2:n.1571-154_1571-153del
NM_001322364.2:c.1583-154_1583-153del NP_001309293.1:n.1583-154_1583-153del
NM_001322365.2:c.1676-154_1676-153del NP_001309294.1:n.1676-154_1676-153del
NM_033496.3:c.1568-154_1568-153del NP_277031.1:n.1568-154_1568-153del
NM_033497.3:c.1583-154_1583-153del NP_277032.1:n.1583-154_1583-153del
NM_033498.3:c.1583-154_1583-153del NP_277033.1:n.1583-154_1583-153del