Canonical Allele Identifier: CA1917771955

Gene: HK1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69382490T= , CM000672.2:g.69382490T=	GRCh38
NC_000010.10:g.71142246T= , CM000672.1:g.71142246T=	GRCh37
NC_000010.9:g.70812252T=	NCBI36
NG_012077.1:g.117491T= , LRG_365:g.117491T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470050.2:c.1269T=	ENSP00000515580.1:p.Tyr423=
ENST00000703945.1:c.1185T=	ENSP00000515578.1:p.Tyr395=
ENST00000703946.1:c.1265+2395T=	ENSP00000515579.1:n.1265+2395T=
ENST00000703947.1:c.879T=	ENSP00000515581.1:p.Tyr293=
ENST00000703948.1:c.*886T=	ENSP00000515582.1:n.*886T=
ENST00000703949.1:c.1269T=	ENSP00000515583.1:p.Tyr423=
ENST00000703950.1:c.1269T=	ENSP00000515584.1:p.Tyr423=
ENST00000703951.1:c.1265+2395T=	ENSP00000515585.1:n.1265+2395T=
ENST00000703952.1:c.1265+2395T=	ENSP00000515586.1:n.1265+2395T=
ENST00000703953.1:c.*532T=	ENSP00000515587.1:n.*532T=
ENST00000703954.1:c.1149T=	ENSP00000515588.1:p.Tyr383=
ENST00000703955.1:n.1819T=
ENST00000298649.8:c.1266T=	ENSP00000298649.3:p.Tyr422=
ENST00000359426.7:c.1269T= MANE Select	ENSP00000352398.6:p.Tyr423=
ENST00000436817.6:c.1281T=	ENSP00000415949.2:p.Tyr427=
ENST00000493591.6:c.*1157T=	ENSP00000494917.1:n.*1157T=
ENST00000643399.2:c.1281T= MANE Plus Clinical	ENSP00000494664.1:p.Tyr427=
ENST00000298649.7:c.1266T=	ENSP00000298649.3:p.Tyr422=
ENST00000359426.6:c.1269T=	ENSP00000352398.6:p.Tyr423=
ENST00000360289.6:c.1233T=	ENSP00000353433.2:p.Tyr411=
ENST00000448642.6:c.1281T=	ENSP00000402103.3:p.Tyr427=
ENST00000494253.1:n.1495T=
NM_000188.2:c.1269T=	NP_000179.2:p.Tyr423=
NM_033496.2:c.1266T=	NP_277031.1:p.Tyr422=
NM_033497.2:c.1281T=	NP_277032.1:p.Tyr427=
NM_033498.2:c.1281T=	NP_277033.1:p.Tyr427=
NM_033500.2:c.1233T= , LRG_365t1:c.1233T=	NP_277035.2:p.Tyr411=
XM_005269735.2:c.1398T=	XP_005269792.1:p.Tyr466=
XM_005269736.1:c.1281T=	XP_005269793.1:p.Tyr427=
XM_005269737.1:c.1185T=	XP_005269794.1:p.Tyr395=
XM_011539732.1:c.1233T=	XP_011538034.1:p.Tyr411=
XM_011539733.1:c.1227T=	XP_011538035.1:p.Tyr409=
XM_011539734.1:c.1224T=	XP_011538036.1:p.Tyr408=
NM_001322364.1:c.1281T=	NP_001309293.1:p.Tyr427=
NM_001322365.1:c.1374T=	NP_001309294.1:p.Tyr458=
NM_001322366.1:c.1185T=	NP_001309295.1:p.Tyr395=
NM_001322367.1:c.1173T=	NP_001309296.1:p.Tyr391=
NM_001358263.1:c.1281T= MANE Plus Clinical	NP_001345192.1:p.Tyr427=
XM_024447969.1:c.1281T=	XP_024303737.1:p.Tyr427=
NM_000188.3:c.1269T= MANE Select	NP_000179.2:p.Tyr423=
NM_001322364.2:c.1281T=	NP_001309293.1:p.Tyr427=
NM_001322365.2:c.1374T=	NP_001309294.1:p.Tyr458=
NM_033496.3:c.1266T=	NP_277031.1:p.Tyr422=
NM_033497.3:c.1281T=	NP_277032.1:p.Tyr427=
NM_033498.3:c.1281T=	NP_277033.1:p.Tyr427=