Canonical Allele Identifier: CA1917773208

Gene: HK1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69384465A= , CM000672.2:g.69384465A=	GRCh38
NC_000010.10:g.71144221A= , CM000672.1:g.71144221A=	GRCh37
NC_000010.9:g.70814227A=	NCBI36
NG_012077.1:g.119466A= , LRG_365:g.119466A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470050.2:c.1703A=	ENSP00000515580.1:p.Gln568=
ENST00000703945.1:c.1619A=	ENSP00000515578.1:p.Gln540=
ENST00000703946.1:c.1265+4370A=	ENSP00000515579.1:n.1265+4370A=
ENST00000703947.1:c.1313A=	ENSP00000515581.1:p.Gln438=
ENST00000703948.1:c.*1320A=	ENSP00000515582.1:n.*1320A=
ENST00000703949.1:c.1703A=	ENSP00000515583.1:p.Gln568=
ENST00000703950.1:c.1703A=	ENSP00000515584.1:p.Gln568=
ENST00000703951.1:c.1265+4370A=	ENSP00000515585.1:n.1265+4370A=
ENST00000703952.1:c.1265+4370A=	ENSP00000515586.1:n.1265+4370A=
ENST00000703953.1:c.*966A=	ENSP00000515587.1:n.*966A=
ENST00000703954.1:c.1583A=	ENSP00000515588.1:p.Gln528=
ENST00000703955.1:n.2253A=
ENST00000703957.1:n.208A=
ENST00000298649.8:c.1700A=	ENSP00000298649.3:p.Gln567=
ENST00000359426.7:c.1703A= MANE Select	ENSP00000352398.6:p.Gln568=
ENST00000436817.6:c.1715A=	ENSP00000415949.2:p.Gln572=
ENST00000493591.6:c.*1591A=	ENSP00000494917.1:n.*1591A=
ENST00000643399.2:c.1715A= MANE Plus Clinical	ENSP00000494664.1:p.Gln572=
ENST00000298649.7:c.1700A=	ENSP00000298649.3:p.Gln567=
ENST00000359426.6:c.1703A=	ENSP00000352398.6:p.Gln568=
ENST00000360289.6:c.1667A=	ENSP00000353433.2:p.Gln556=
ENST00000448642.6:c.1715A=	ENSP00000402103.3:p.Gln572=
ENST00000494253.1:n.1929A=
NM_000188.2:c.1703A=	NP_000179.2:p.Gln568=
NM_033496.2:c.1700A=	NP_277031.1:p.Gln567=
NM_033497.2:c.1715A=	NP_277032.1:p.Gln572=
NM_033498.2:c.1715A=	NP_277033.1:p.Gln572=
NM_033500.2:c.1667A= , LRG_365t1:c.1667A=	NP_277035.2:p.Gln556=
XM_005269735.2:c.1832A=	XP_005269792.1:p.Gln611=
XM_005269736.1:c.1715A=	XP_005269793.1:p.Gln572=
XM_005269737.1:c.1619A=	XP_005269794.1:p.Gln540=
XM_011539732.1:c.1667A=	XP_011538034.1:p.Gln556=
XM_011539733.1:c.1661A=	XP_011538035.1:p.Gln554=
XM_011539734.1:c.1658A=	XP_011538036.1:p.Gln553=
NM_001322364.1:c.1715A=	NP_001309293.1:p.Gln572=
NM_001322365.1:c.1808A=	NP_001309294.1:p.Gln603=
NM_001322366.1:c.1619A=	NP_001309295.1:p.Gln540=
NM_001322367.1:c.1607A=	NP_001309296.1:p.Gln536=
NM_001358263.1:c.1715A= MANE Plus Clinical	NP_001345192.1:p.Gln572=
XM_024447969.1:c.1715A=	XP_024303737.1:p.Gln572=
NM_000188.3:c.1703A= MANE Select	NP_000179.2:p.Gln568=
NM_001322364.2:c.1715A=	NP_001309293.1:p.Gln572=
NM_001322365.2:c.1808A=	NP_001309294.1:p.Gln603=
NM_033496.3:c.1700A=	NP_277031.1:p.Gln567=
NM_033497.3:c.1715A=	NP_277032.1:p.Gln572=
NM_033498.3:c.1715A=	NP_277033.1:p.Gln572=