Canonical Allele Identifier: CA1917772309

Gene: HK1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69382766C= , CM000672.2:g.69382766C=	GRCh38
NC_000010.10:g.71142522C= , CM000672.1:g.71142522C=	GRCh37
NC_000010.9:g.70812528C=	NCBI36
NG_012077.1:g.117767C= , LRG_365:g.117767C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470050.2:c.1545C=	ENSP00000515580.1:p.Phe515=
ENST00000703945.1:c.1461C=	ENSP00000515578.1:p.Phe487=
ENST00000703946.1:c.1265+2671C=	ENSP00000515579.1:n.1265+2671C=
ENST00000703947.1:c.1155C=	ENSP00000515581.1:p.Phe385=
ENST00000703948.1:c.*1162C=	ENSP00000515582.1:n.*1162C=
ENST00000703949.1:c.1545C=	ENSP00000515583.1:p.Phe515=
ENST00000703950.1:c.1545C=	ENSP00000515584.1:p.Phe515=
ENST00000703951.1:c.1265+2671C=	ENSP00000515585.1:n.1265+2671C=
ENST00000703952.1:c.1265+2671C=	ENSP00000515586.1:n.1265+2671C=
ENST00000703953.1:c.*808C=	ENSP00000515587.1:n.*808C=
ENST00000703954.1:c.1425C=	ENSP00000515588.1:p.Phe475=
ENST00000703955.1:n.2095C=
ENST00000703957.1:n.50C=
ENST00000298649.8:c.1542C=	ENSP00000298649.3:p.Phe514=
ENST00000359426.7:c.1545C= MANE Select	ENSP00000352398.6:p.Phe515=
ENST00000436817.6:c.1557C=	ENSP00000415949.2:p.Phe519=
ENST00000493591.6:c.*1433C=	ENSP00000494917.1:n.*1433C=
ENST00000643399.2:c.1557C= MANE Plus Clinical	ENSP00000494664.1:p.Phe519=
ENST00000298649.7:c.1542C=	ENSP00000298649.3:p.Phe514=
ENST00000359426.6:c.1545C=	ENSP00000352398.6:p.Phe515=
ENST00000360289.6:c.1509C=	ENSP00000353433.2:p.Phe503=
ENST00000448642.6:c.1557C=	ENSP00000402103.3:p.Phe519=
ENST00000494253.1:n.1771C=
NM_000188.2:c.1545C=	NP_000179.2:p.Phe515=
NM_033496.2:c.1542C=	NP_277031.1:p.Phe514=
NM_033497.2:c.1557C=	NP_277032.1:p.Phe519=
NM_033498.2:c.1557C=	NP_277033.1:p.Phe519=
NM_033500.2:c.1509C= , LRG_365t1:c.1509C=	NP_277035.2:p.Phe503=
XM_005269735.2:c.1674C=	XP_005269792.1:p.Phe558=
XM_005269736.1:c.1557C=	XP_005269793.1:p.Phe519=
XM_005269737.1:c.1461C=	XP_005269794.1:p.Phe487=
XM_011539732.1:c.1509C=	XP_011538034.1:p.Phe503=
XM_011539733.1:c.1503C=	XP_011538035.1:p.Phe501=
XM_011539734.1:c.1500C=	XP_011538036.1:p.Phe500=
NM_001322364.1:c.1557C=	NP_001309293.1:p.Phe519=
NM_001322365.1:c.1650C=	NP_001309294.1:p.Phe550=
NM_001322366.1:c.1461C=	NP_001309295.1:p.Phe487=
NM_001322367.1:c.1449C=	NP_001309296.1:p.Phe483=
NM_001358263.1:c.1557C= MANE Plus Clinical	NP_001345192.1:p.Phe519=
XM_024447969.1:c.1557C=	XP_024303737.1:p.Phe519=
NM_000188.3:c.1545C= MANE Select	NP_000179.2:p.Phe515=
NM_001322364.2:c.1557C=	NP_001309293.1:p.Phe519=
NM_001322365.2:c.1650C=	NP_001309294.1:p.Phe550=
NM_033496.3:c.1542C=	NP_277031.1:p.Phe514=
NM_033497.3:c.1557C=	NP_277032.1:p.Phe519=
NM_033498.3:c.1557C=	NP_277033.1:p.Phe519=