Canonical Allele Identifier: CA1917772232

Gene: HK1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69382690G= , CM000672.2:g.69382690G=	GRCh38
NC_000010.10:g.71142446G= , CM000672.1:g.71142446G=	GRCh37
NC_000010.9:g.70812452G=	NCBI36
NG_012077.1:g.117691G= , LRG_365:g.117691G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470050.2:c.1469G=	ENSP00000515580.1:p.Arg490=
ENST00000703945.1:c.1385G=	ENSP00000515578.1:p.Arg462=
ENST00000703946.1:c.1265+2595G=	ENSP00000515579.1:n.1265+2595G=
ENST00000703947.1:c.1079G=	ENSP00000515581.1:p.Arg360=
ENST00000703948.1:c.*1086G=	ENSP00000515582.1:n.*1086G=
ENST00000703949.1:c.1469G=	ENSP00000515583.1:p.Arg490=
ENST00000703950.1:c.1469G=	ENSP00000515584.1:p.Arg490=
ENST00000703951.1:c.1265+2595G=	ENSP00000515585.1:n.1265+2595G=
ENST00000703952.1:c.1265+2595G=	ENSP00000515586.1:n.1265+2595G=
ENST00000703953.1:c.*732G=	ENSP00000515587.1:n.*732G=
ENST00000703954.1:c.1349G=	ENSP00000515588.1:p.Arg450=
ENST00000703955.1:n.2019G=
ENST00000298649.8:c.1466G=	ENSP00000298649.3:p.Arg489=
ENST00000359426.7:c.1469G= MANE Select	ENSP00000352398.6:p.Arg490=
ENST00000436817.6:c.1481G=	ENSP00000415949.2:p.Arg494=
ENST00000493591.6:c.*1357G=	ENSP00000494917.1:n.*1357G=
ENST00000643399.2:c.1481G= MANE Plus Clinical	ENSP00000494664.1:p.Arg494=
ENST00000298649.7:c.1466G=	ENSP00000298649.3:p.Arg489=
ENST00000359426.6:c.1469G=	ENSP00000352398.6:p.Arg490=
ENST00000360289.6:c.1433G=	ENSP00000353433.2:p.Arg478=
ENST00000448642.6:c.1481G=	ENSP00000402103.3:p.Arg494=
ENST00000494253.1:n.1695G=
NM_000188.2:c.1469G=	NP_000179.2:p.Arg490=
NM_033496.2:c.1466G=	NP_277031.1:p.Arg489=
NM_033497.2:c.1481G=	NP_277032.1:p.Arg494=
NM_033498.2:c.1481G=	NP_277033.1:p.Arg494=
NM_033500.2:c.1433G= , LRG_365t1:c.1433G=	NP_277035.2:p.Arg478=
XM_005269735.2:c.1598G=	XP_005269792.1:p.Arg533=
XM_005269736.1:c.1481G=	XP_005269793.1:p.Arg494=
XM_005269737.1:c.1385G=	XP_005269794.1:p.Arg462=
XM_011539732.1:c.1433G=	XP_011538034.1:p.Arg478=
XM_011539733.1:c.1427G=	XP_011538035.1:p.Arg476=
XM_011539734.1:c.1424G=	XP_011538036.1:p.Arg475=
NM_001322364.1:c.1481G=	NP_001309293.1:p.Arg494=
NM_001322365.1:c.1574G=	NP_001309294.1:p.Arg525=
NM_001322366.1:c.1385G=	NP_001309295.1:p.Arg462=
NM_001322367.1:c.1373G=	NP_001309296.1:p.Arg458=
NM_001358263.1:c.1481G= MANE Plus Clinical	NP_001345192.1:p.Arg494=
XM_024447969.1:c.1481G=	XP_024303737.1:p.Arg494=
NM_000188.3:c.1469G= MANE Select	NP_000179.2:p.Arg490=
NM_001322364.2:c.1481G=	NP_001309293.1:p.Arg494=
NM_001322365.2:c.1574G=	NP_001309294.1:p.Arg525=
NM_033496.3:c.1466G=	NP_277031.1:p.Arg489=
NM_033497.3:c.1481G=	NP_277032.1:p.Arg494=
NM_033498.3:c.1481G=	NP_277033.1:p.Arg494=