Canonical Allele Identifier: CA1917773160
Gene: HK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.69384348T= , CM000672.2:g.69384348T= GRCh38
NC_000010.10:g.71144104T= , CM000672.1:g.71144104T= GRCh37
NC_000010.9:g.70814110T= NCBI36
NG_012077.1:g.119349T= , LRG_365:g.119349T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000470050.2:c.1586T= ENSP00000515580.1:p.Leu529=
ENST00000703945.1:c.1502T= ENSP00000515578.1:p.Leu501=
ENST00000703946.1:c.1265+4253T= ENSP00000515579.1:n.1265+4253T=
ENST00000703947.1:c.1196T= ENSP00000515581.1:p.Leu399=
ENST00000703948.1:c.*1203T= ENSP00000515582.1:n.*1203T=
ENST00000703949.1:c.1586T= ENSP00000515583.1:p.Leu529=
ENST00000703950.1:c.1586T= ENSP00000515584.1:p.Leu529=
ENST00000703951.1:c.1265+4253T= ENSP00000515585.1:n.1265+4253T=
ENST00000703952.1:c.1265+4253T= ENSP00000515586.1:n.1265+4253T=
ENST00000703953.1:c.*849T= ENSP00000515587.1:n.*849T=
ENST00000703954.1:c.1466T= ENSP00000515588.1:p.Leu489=
ENST00000703955.1:n.2136T=
ENST00000703957.1:n.91T=
ENST00000298649.8:c.1583T= ENSP00000298649.3:p.Leu528=
ENST00000359426.7:c.1586T= MANE Select ENSP00000352398.6:p.Leu529=
ENST00000436817.6:c.1598T= ENSP00000415949.2:p.Leu533=
ENST00000493591.6:c.*1474T= ENSP00000494917.1:n.*1474T=
ENST00000643399.2:c.1598T= MANE Plus Clinical ENSP00000494664.1:p.Leu533=
ENST00000298649.7:c.1583T= ENSP00000298649.3:p.Leu528=
ENST00000359426.6:c.1586T= ENSP00000352398.6:p.Leu529=
ENST00000360289.6:c.1550T= ENSP00000353433.2:p.Leu517=
ENST00000448642.6:c.1598T= ENSP00000402103.3:p.Leu533=
ENST00000494253.1:n.1812T=
NM_000188.2:c.1586T= NP_000179.2:p.Leu529=
NM_033496.2:c.1583T= NP_277031.1:p.Leu528=
NM_033497.2:c.1598T= NP_277032.1:p.Leu533=
NM_033498.2:c.1598T= NP_277033.1:p.Leu533=
NM_033500.2:c.1550T= , LRG_365t1:c.1550T= NP_277035.2:p.Leu517=
XM_005269735.2:c.1715T= XP_005269792.1:p.Leu572=
XM_005269736.1:c.1598T= XP_005269793.1:p.Leu533=
XM_005269737.1:c.1502T= XP_005269794.1:p.Leu501=
XM_011539732.1:c.1550T= XP_011538034.1:p.Leu517=
XM_011539733.1:c.1544T= XP_011538035.1:p.Leu515=
XM_011539734.1:c.1541T= XP_011538036.1:p.Leu514=
NM_001322364.1:c.1598T= NP_001309293.1:p.Leu533=
NM_001322365.1:c.1691T= NP_001309294.1:p.Leu564=
NM_001322366.1:c.1502T= NP_001309295.1:p.Leu501=
NM_001322367.1:c.1490T= NP_001309296.1:p.Leu497=
NM_001358263.1:c.1598T= MANE Plus Clinical NP_001345192.1:p.Leu533=
XM_024447969.1:c.1598T= XP_024303737.1:p.Leu533=
NM_000188.3:c.1586T= MANE Select NP_000179.2:p.Leu529=
NM_001322364.2:c.1598T= NP_001309293.1:p.Leu533=
NM_001322365.2:c.1691T= NP_001309294.1:p.Leu564=
NM_033496.3:c.1583T= NP_277031.1:p.Leu528=
NM_033497.3:c.1598T= NP_277032.1:p.Leu533=
NM_033498.3:c.1598T= NP_277033.1:p.Leu533=