Canonical Allele Identifier: CA1917771981

Gene: HK1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69382510C= , CM000672.2:g.69382510C=	GRCh38
NC_000010.10:g.71142266C= , CM000672.1:g.71142266C=	GRCh37
NC_000010.9:g.70812272C=	NCBI36
NG_012077.1:g.117511C= , LRG_365:g.117511C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470050.2:c.1289C=	ENSP00000515580.1:p.Thr430=
ENST00000703945.1:c.1205C=	ENSP00000515578.1:p.Thr402=
ENST00000703946.1:c.1265+2415C=	ENSP00000515579.1:n.1265+2415C=
ENST00000703947.1:c.899C=	ENSP00000515581.1:p.Thr300=
ENST00000703948.1:c.*906C=	ENSP00000515582.1:n.*906C=
ENST00000703949.1:c.1289C=	ENSP00000515583.1:p.Thr430=
ENST00000703950.1:c.1289C=	ENSP00000515584.1:p.Thr430=
ENST00000703951.1:c.1265+2415C=	ENSP00000515585.1:n.1265+2415C=
ENST00000703952.1:c.1265+2415C=	ENSP00000515586.1:n.1265+2415C=
ENST00000703953.1:c.*552C=	ENSP00000515587.1:n.*552C=
ENST00000703954.1:c.1169C=	ENSP00000515588.1:p.Thr390=
ENST00000703955.1:n.1839C=
ENST00000298649.8:c.1286C=	ENSP00000298649.3:p.Thr429=
ENST00000359426.7:c.1289C= MANE Select	ENSP00000352398.6:p.Thr430=
ENST00000436817.6:c.1301C=	ENSP00000415949.2:p.Thr434=
ENST00000493591.6:c.*1177C=	ENSP00000494917.1:n.*1177C=
ENST00000643399.2:c.1301C= MANE Plus Clinical	ENSP00000494664.1:p.Thr434=
ENST00000298649.7:c.1286C=	ENSP00000298649.3:p.Thr429=
ENST00000359426.6:c.1289C=	ENSP00000352398.6:p.Thr430=
ENST00000360289.6:c.1253C=	ENSP00000353433.2:p.Thr418=
ENST00000448642.6:c.1301C=	ENSP00000402103.3:p.Thr434=
ENST00000494253.1:n.1515C=
NM_000188.2:c.1289C=	NP_000179.2:p.Thr430=
NM_033496.2:c.1286C=	NP_277031.1:p.Thr429=
NM_033497.2:c.1301C=	NP_277032.1:p.Thr434=
NM_033498.2:c.1301C=	NP_277033.1:p.Thr434=
NM_033500.2:c.1253C= , LRG_365t1:c.1253C=	NP_277035.2:p.Thr418=
XM_005269735.2:c.1418C=	XP_005269792.1:p.Thr473=
XM_005269736.1:c.1301C=	XP_005269793.1:p.Thr434=
XM_005269737.1:c.1205C=	XP_005269794.1:p.Thr402=
XM_011539732.1:c.1253C=	XP_011538034.1:p.Thr418=
XM_011539733.1:c.1247C=	XP_011538035.1:p.Thr416=
XM_011539734.1:c.1244C=	XP_011538036.1:p.Thr415=
NM_001322364.1:c.1301C=	NP_001309293.1:p.Thr434=
NM_001322365.1:c.1394C=	NP_001309294.1:p.Thr465=
NM_001322366.1:c.1205C=	NP_001309295.1:p.Thr402=
NM_001322367.1:c.1193C=	NP_001309296.1:p.Thr398=
NM_001358263.1:c.1301C= MANE Plus Clinical	NP_001345192.1:p.Thr434=
XM_024447969.1:c.1301C=	XP_024303737.1:p.Thr434=
NM_000188.3:c.1289C= MANE Select	NP_000179.2:p.Thr430=
NM_001322364.2:c.1301C=	NP_001309293.1:p.Thr434=
NM_001322365.2:c.1394C=	NP_001309294.1:p.Thr465=
NM_033496.3:c.1286C=	NP_277031.1:p.Thr429=
NM_033497.3:c.1301C=	NP_277032.1:p.Thr434=
NM_033498.3:c.1301C=	NP_277033.1:p.Thr434=