Canonical Allele Identifier: CA5532404

Gene: HK1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69369349C>T , CM000672.2:g.69369349C>T	GRCh38
NC_000010.10:g.71129105C>T , CM000672.1:g.71129105C>T	GRCh37
NC_000010.9:g.70799111C>T	NCBI36
NG_012077.1:g.104350C>T , LRG_365:g.104350C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470050.2:c.691+13C>T	ENSP00000515580.1:n.691+13C>T
ENST00000703944.1:c.703+13C>T	ENSP00000515576.1:n.703+13C>T
ENST00000703945.1:c.607+13C>T	ENSP00000515578.1:n.607+13C>T
ENST00000703946.1:c.691+13C>T	ENSP00000515579.1:n.691+13C>T
ENST00000703947.1:c.691+13C>T	ENSP00000515581.1:n.691+13C>T
ENST00000703948.1:c.*308+13C>T	ENSP00000515582.1:n.*308+13C>T
ENST00000703949.1:c.691+13C>T	ENSP00000515583.1:n.691+13C>T
ENST00000703950.1:c.691+13C>T	ENSP00000515584.1:n.691+13C>T
ENST00000703951.1:c.691+13C>T	ENSP00000515585.1:n.691+13C>T
ENST00000703952.1:c.691+13C>T	ENSP00000515586.1:n.691+13C>T
ENST00000703953.1:c.691+13C>T	ENSP00000515587.1:n.691+13C>T
ENST00000703954.1:c.571+13C>T	ENSP00000515588.1:n.571+13C>T
ENST00000703955.1:n.1241+13C>T
ENST00000703956.1:n.503+13C>T
ENST00000298649.8:c.688+13C>T	ENSP00000298649.3:n.688+13C>T
ENST00000359426.7:c.691+13C>T MANE Select	ENSP00000352398.6:n.691+13C>T
ENST00000436817.6:c.703+13C>T	ENSP00000415949.2:n.703+13C>T
ENST00000493591.6:c.*579+13C>T	ENSP00000494917.1:n.*579+13C>T
ENST00000643399.2:c.703+13C>T MANE Plus Clinical	ENSP00000494664.1:n.703+13C>T
ENST00000298649.7:c.688+13C>T	ENSP00000298649.3:n.688+13C>T
ENST00000359426.6:c.691+13C>T	ENSP00000352398.6:n.691+13C>T
ENST00000360289.6:c.655+13C>T	ENSP00000353433.2:n.655+13C>T
ENST00000436817.5:c.688+13C>T	ENSP00000415949.1:n.688+13C>T
ENST00000448642.6:c.703+13C>T	ENSP00000402103.3:n.703+13C>T
ENST00000493591.5:n.695+13C>T
ENST00000494253.1:n.917+13C>T
NM_000188.2:c.691+13C>T	NP_000179.2:n.691+13C>T
NM_033496.2:c.688+13C>T	NP_277031.1:n.688+13C>T
NM_033497.2:c.703+13C>T	NP_277032.1:n.703+13C>T
NM_033498.2:c.703+13C>T	NP_277033.1:n.703+13C>T
NM_033500.2:c.655+13C>T , LRG_365t1:c.655+13C>T	NP_277035.2:n.655+13C>T
XM_005269735.2:c.820+13C>T	XP_005269792.1:n.820+13C>T
XM_005269736.1:c.703+13C>T	XP_005269793.1:n.703+13C>T
XM_005269737.1:c.607+13C>T	XP_005269794.1:n.607+13C>T
XM_011539732.1:c.655+13C>T	XP_011538034.1:n.655+13C>T
XM_011539733.1:c.649+13C>T	XP_011538035.1:n.649+13C>T
XM_011539734.1:c.646+13C>T	XP_011538036.1:n.646+13C>T
NM_001322364.1:c.703+13C>T	NP_001309293.1:n.703+13C>T
NM_001322365.1:c.796+13C>T	NP_001309294.1:n.796+13C>T
NM_001322366.1:c.607+13C>T	NP_001309295.1:n.607+13C>T
NM_001322367.1:c.595+13C>T	NP_001309296.1:n.595+13C>T
NM_001358263.1:c.703+13C>T MANE Plus Clinical	NP_001345192.1:n.703+13C>T
XM_024447969.1:c.703+13C>T	XP_024303737.1:n.703+13C>T
NM_000188.3:c.691+13C>T MANE Select	NP_000179.2:n.691+13C>T
NM_001322364.2:c.703+13C>T	NP_001309293.1:n.703+13C>T
NM_001322365.2:c.796+13C>T	NP_001309294.1:n.796+13C>T
NM_033496.3:c.688+13C>T	NP_277031.1:n.688+13C>T
NM_033497.3:c.703+13C>T	NP_277032.1:n.703+13C>T
NM_033498.3:c.703+13C>T	NP_277033.1:n.703+13C>T