Canonical Allele Identifier: CA2609447354
Gene: HK1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.69384582_69384587del , CM000672.2:g.69384582_69384587del GRCh38
NC_000010.10:g.71144338_71144343del , CM000672.1:g.71144338_71144343del GRCh37
NC_000010.9:g.70814344_70814349del NCBI36
NG_012077.1:g.119583_119588del , LRG_365:g.119583_119588del

Transcript Alleles

HGVS Amino-acid Change
ENST00000470050.2:c.1719+101_1719+106del ENSP00000515580.1:n.1719+101_1719+106del
ENST00000703945.1:c.1635+101_1635+106del ENSP00000515578.1:n.1635+101_1635+106del
ENST00000703946.1:c.1265+4487_1265+4492del ENSP00000515579.1:n.1265+4487_1265+4492del
ENST00000703947.1:c.1329+101_1329+106del ENSP00000515581.1:n.1329+101_1329+106del
ENST00000703948.1:c.*1336+101_*1336+106del ENSP00000515582.1:n.*1336+101_*1336+106del
ENST00000703949.1:c.1719+101_1719+106del ENSP00000515583.1:n.1719+101_1719+106del
ENST00000703950.1:c.1719+101_1719+106del ENSP00000515584.1:n.1719+101_1719+106del
ENST00000703951.1:c.1265+4487_1265+4492del ENSP00000515585.1:n.1265+4487_1265+4492del
ENST00000703952.1:c.1265+4487_1265+4492del ENSP00000515586.1:n.1265+4487_1265+4492del
ENST00000703953.1:c.*982+101_*982+106del ENSP00000515587.1:n.*982+101_*982+106del
ENST00000703954.1:c.1599+101_1599+106del ENSP00000515588.1:n.1599+101_1599+106del
ENST00000703955.1:n.2269+101_2269+106del
ENST00000703957.1:n.224+101_224+106del
ENST00000298649.8:c.1716+101_1716+106del ENSP00000298649.3:n.1716+101_1716+106del
ENST00000359426.7:c.1719+101_1719+106del MANE Select ENSP00000352398.6:n.1719+101_1719+106del
ENST00000436817.6:c.1731+101_1731+106del ENSP00000415949.2:n.1731+101_1731+106del
ENST00000493591.6:c.*1607+101_*1607+106del ENSP00000494917.1:n.*1607+101_*1607+106del
ENST00000643399.2:c.1731+101_1731+106del MANE Plus Clinical ENSP00000494664.1:n.1731+101_1731+106del
ENST00000298649.7:c.1716+101_1716+106del ENSP00000298649.3:n.1716+101_1716+106del
ENST00000359426.6:c.1719+101_1719+106del ENSP00000352398.6:n.1719+101_1719+106del
ENST00000360289.6:c.1683+101_1683+106del ENSP00000353433.2:n.1683+101_1683+106del
ENST00000448642.6:c.1731+101_1731+106del ENSP00000402103.3:n.1731+101_1731+106del
ENST00000494253.1:n.2046_2051del
NM_000188.2:c.1719+101_1719+106del NP_000179.2:n.1719+101_1719+106del
NM_033496.2:c.1716+101_1716+106del NP_277031.1:n.1716+101_1716+106del
NM_033497.2:c.1731+101_1731+106del NP_277032.1:n.1731+101_1731+106del
NM_033498.2:c.1731+101_1731+106del NP_277033.1:n.1731+101_1731+106del
NM_033500.2:c.1683+101_1683+106del , LRG_365t1:c.1683+101_1683+106del NP_277035.2:n.1683+101_1683+106del
XM_005269735.2:c.1848+101_1848+106del XP_005269792.1:n.1848+101_1848+106del
XM_005269736.1:c.1731+101_1731+106del XP_005269793.1:n.1731+101_1731+106del
XM_005269737.1:c.1635+101_1635+106del XP_005269794.1:n.1635+101_1635+106del
XM_011539732.1:c.1683+101_1683+106del XP_011538034.1:n.1683+101_1683+106del
XM_011539733.1:c.1677+101_1677+106del XP_011538035.1:n.1677+101_1677+106del
XM_011539734.1:c.1674+101_1674+106del XP_011538036.1:n.1674+101_1674+106del
NM_001322364.1:c.1731+101_1731+106del NP_001309293.1:n.1731+101_1731+106del
NM_001322365.1:c.1824+101_1824+106del NP_001309294.1:n.1824+101_1824+106del
NM_001322366.1:c.1635+101_1635+106del NP_001309295.1:n.1635+101_1635+106del
NM_001322367.1:c.1623+101_1623+106del NP_001309296.1:n.1623+101_1623+106del
NM_001358263.1:c.1731+101_1731+106del MANE Plus Clinical NP_001345192.1:n.1731+101_1731+106del
XM_024447969.1:c.1731+101_1731+106del XP_024303737.1:n.1731+101_1731+106del
NM_000188.3:c.1719+101_1719+106del MANE Select NP_000179.2:n.1719+101_1719+106del
NM_001322364.2:c.1731+101_1731+106del NP_001309293.1:n.1731+101_1731+106del
NM_001322365.2:c.1824+101_1824+106del NP_001309294.1:n.1824+101_1824+106del
NM_033496.3:c.1716+101_1716+106del NP_277031.1:n.1716+101_1716+106del
NM_033497.3:c.1731+101_1731+106del NP_277032.1:n.1731+101_1731+106del
NM_033498.3:c.1731+101_1731+106del NP_277033.1:n.1731+101_1731+106del