Canonical Allele Identifier: CA1917773172
Gene: HK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.69384378G= , CM000672.2:g.69384378G= GRCh38
NC_000010.10:g.71144134G= , CM000672.1:g.71144134G= GRCh37
NC_000010.9:g.70814140G= NCBI36
NG_012077.1:g.119379G= , LRG_365:g.119379G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000470050.2:c.1616G= ENSP00000515580.1:p.Arg539=
ENST00000703945.1:c.1532G= ENSP00000515578.1:p.Arg511=
ENST00000703946.1:c.1265+4283G= ENSP00000515579.1:n.1265+4283G=
ENST00000703947.1:c.1226G= ENSP00000515581.1:p.Arg409=
ENST00000703948.1:c.*1233G= ENSP00000515582.1:n.*1233G=
ENST00000703949.1:c.1616G= ENSP00000515583.1:p.Arg539=
ENST00000703950.1:c.1616G= ENSP00000515584.1:p.Arg539=
ENST00000703951.1:c.1265+4283G= ENSP00000515585.1:n.1265+4283G=
ENST00000703952.1:c.1265+4283G= ENSP00000515586.1:n.1265+4283G=
ENST00000703953.1:c.*879G= ENSP00000515587.1:n.*879G=
ENST00000703954.1:c.1496G= ENSP00000515588.1:p.Arg499=
ENST00000703955.1:n.2166G=
ENST00000703957.1:n.121G=
ENST00000298649.8:c.1613G= ENSP00000298649.3:p.Arg538=
ENST00000359426.7:c.1616G= MANE Select ENSP00000352398.6:p.Arg539=
ENST00000436817.6:c.1628G= ENSP00000415949.2:p.Arg543=
ENST00000493591.6:c.*1504G= ENSP00000494917.1:n.*1504G=
ENST00000643399.2:c.1628G= MANE Plus Clinical ENSP00000494664.1:p.Arg543=
ENST00000298649.7:c.1613G= ENSP00000298649.3:p.Arg538=
ENST00000359426.6:c.1616G= ENSP00000352398.6:p.Arg539=
ENST00000360289.6:c.1580G= ENSP00000353433.2:p.Arg527=
ENST00000448642.6:c.1628G= ENSP00000402103.3:p.Arg543=
ENST00000494253.1:n.1842G=
NM_000188.2:c.1616G= NP_000179.2:p.Arg539=
NM_033496.2:c.1613G= NP_277031.1:p.Arg538=
NM_033497.2:c.1628G= NP_277032.1:p.Arg543=
NM_033498.2:c.1628G= NP_277033.1:p.Arg543=
NM_033500.2:c.1580G= , LRG_365t1:c.1580G= NP_277035.2:p.Arg527=
XM_005269735.2:c.1745G= XP_005269792.1:p.Arg582=
XM_005269736.1:c.1628G= XP_005269793.1:p.Arg543=
XM_005269737.1:c.1532G= XP_005269794.1:p.Arg511=
XM_011539732.1:c.1580G= XP_011538034.1:p.Arg527=
XM_011539733.1:c.1574G= XP_011538035.1:p.Arg525=
XM_011539734.1:c.1571G= XP_011538036.1:p.Arg524=
NM_001322364.1:c.1628G= NP_001309293.1:p.Arg543=
NM_001322365.1:c.1721G= NP_001309294.1:p.Arg574=
NM_001322366.1:c.1532G= NP_001309295.1:p.Arg511=
NM_001322367.1:c.1520G= NP_001309296.1:p.Arg507=
NM_001358263.1:c.1628G= MANE Plus Clinical NP_001345192.1:p.Arg543=
XM_024447969.1:c.1628G= XP_024303737.1:p.Arg543=
NM_000188.3:c.1616G= MANE Select NP_000179.2:p.Arg539=
NM_001322364.2:c.1628G= NP_001309293.1:p.Arg543=
NM_001322365.2:c.1721G= NP_001309294.1:p.Arg574=
NM_033496.3:c.1613G= NP_277031.1:p.Arg538=
NM_033497.3:c.1628G= NP_277032.1:p.Arg543=
NM_033498.3:c.1628G= NP_277033.1:p.Arg543=