Canonical Allele Identifier: CA1917773344
Gene: HK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.69384663A= , CM000672.2:g.69384663A= GRCh38
NC_000010.10:g.71144419A= , CM000672.1:g.71144419A= GRCh37
NC_000010.9:g.70814425A= NCBI36
NG_012077.1:g.119664A= , LRG_365:g.119664A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000470050.2:c.1720-133A= ENSP00000515580.1:n.1720-133A=
ENST00000703945.1:c.1636-133A= ENSP00000515578.1:n.1636-133A=
ENST00000703946.1:c.1265+4568A= ENSP00000515579.1:n.1265+4568A=
ENST00000703947.1:c.1330-133A= ENSP00000515581.1:n.1330-133A=
ENST00000703948.1:c.*1337-133A= ENSP00000515582.1:n.*1337-133A=
ENST00000703949.1:c.1720-133A= ENSP00000515583.1:n.1720-133A=
ENST00000703950.1:c.1720-133A= ENSP00000515584.1:n.1720-133A=
ENST00000703951.1:c.1265+4568A= ENSP00000515585.1:n.1265+4568A=
ENST00000703952.1:c.1265+4568A= ENSP00000515586.1:n.1265+4568A=
ENST00000703953.1:c.*983-133A= ENSP00000515587.1:n.*983-133A=
ENST00000703954.1:c.1600-133A= ENSP00000515588.1:n.1600-133A=
ENST00000703955.1:n.2270-133A=
ENST00000703957.1:n.225-133A=
ENST00000298649.8:c.1717-133A= ENSP00000298649.3:n.1717-133A=
ENST00000359426.7:c.1720-133A= MANE Select ENSP00000352398.6:n.1720-133A=
ENST00000436817.6:c.1732-133A= ENSP00000415949.2:n.1732-133A=
ENST00000493591.6:c.*1608-133A= ENSP00000494917.1:n.*1608-133A=
ENST00000643399.2:c.1732-133A= MANE Plus Clinical ENSP00000494664.1:n.1732-133A=
ENST00000298649.7:c.1717-133A= ENSP00000298649.3:n.1717-133A=
ENST00000359426.6:c.1720-133A= ENSP00000352398.6:n.1720-133A=
ENST00000360289.6:c.1684-133A= ENSP00000353433.2:n.1684-133A=
ENST00000448642.6:c.1732-133A= ENSP00000402103.3:n.1732-133A=
ENST00000494253.1:n.2127A=
NM_000188.2:c.1720-133A= NP_000179.2:n.1720-133A=
NM_033496.2:c.1717-133A= NP_277031.1:n.1717-133A=
NM_033497.2:c.1732-133A= NP_277032.1:n.1732-133A=
NM_033498.2:c.1732-133A= NP_277033.1:n.1732-133A=
NM_033500.2:c.1684-133A= , LRG_365t1:c.1684-133A= NP_277035.2:n.1684-133A=
XM_005269735.2:c.1849-133A= XP_005269792.1:n.1849-133A=
XM_005269736.1:c.1732-133A= XP_005269793.1:n.1732-133A=
XM_005269737.1:c.1636-133A= XP_005269794.1:n.1636-133A=
XM_011539732.1:c.1684-133A= XP_011538034.1:n.1684-133A=
XM_011539733.1:c.1678-133A= XP_011538035.1:n.1678-133A=
XM_011539734.1:c.1675-133A= XP_011538036.1:n.1675-133A=
NM_001322364.1:c.1732-133A= NP_001309293.1:n.1732-133A=
NM_001322365.1:c.1825-133A= NP_001309294.1:n.1825-133A=
NM_001322366.1:c.1636-133A= NP_001309295.1:n.1636-133A=
NM_001322367.1:c.1624-133A= NP_001309296.1:n.1624-133A=
NM_001358263.1:c.1732-133A= MANE Plus Clinical NP_001345192.1:n.1732-133A=
XM_024447969.1:c.1732-133A= XP_024303737.1:n.1732-133A=
NM_000188.3:c.1720-133A= MANE Select NP_000179.2:n.1720-133A=
NM_001322364.2:c.1732-133A= NP_001309293.1:n.1732-133A=
NM_001322365.2:c.1825-133A= NP_001309294.1:n.1825-133A=
NM_033496.3:c.1717-133A= NP_277031.1:n.1717-133A=
NM_033497.3:c.1732-133A= NP_277032.1:n.1732-133A=
NM_033498.3:c.1732-133A= NP_277033.1:n.1732-133A=