Canonical Allele Identifier: CA376911373

Gene: HK1

Linked Data

• MyVariant Identifiers: chr10:g.71144191A>G (hg19) ; chr10:g.69384435A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69384435A>G , CM000672.2:g.69384435A>G	GRCh38
NC_000010.10:g.71144191A>G , CM000672.1:g.71144191A>G	GRCh37
NC_000010.9:g.70814197A>G	NCBI36
NG_012077.1:g.119436A>G , LRG_365:g.119436A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470050.2:c.1673A>G	ENSP00000515580.1:p.Lys558Arg
ENST00000703945.1:c.1589A>G	ENSP00000515578.1:p.Lys530Arg
ENST00000703946.1:c.1265+4340A>G	ENSP00000515579.1:n.1265+4340A>G
ENST00000703947.1:c.1283A>G	ENSP00000515581.1:p.Lys428Arg
ENST00000703948.1:c.*1290A>G	ENSP00000515582.1:n.*1290A>G
ENST00000703949.1:c.1673A>G	ENSP00000515583.1:p.Lys558Arg
ENST00000703950.1:c.1673A>G	ENSP00000515584.1:p.Lys558Arg
ENST00000703951.1:c.1265+4340A>G	ENSP00000515585.1:n.1265+4340A>G
ENST00000703952.1:c.1265+4340A>G	ENSP00000515586.1:n.1265+4340A>G
ENST00000703953.1:c.*936A>G	ENSP00000515587.1:n.*936A>G
ENST00000703954.1:c.1553A>G	ENSP00000515588.1:p.Lys518Arg
ENST00000703955.1:n.2223A>G
ENST00000703957.1:n.178A>G
ENST00000298649.8:c.1670A>G	ENSP00000298649.3:p.Lys557Arg
ENST00000359426.7:c.1673A>G MANE Select	ENSP00000352398.6:p.Lys558Arg
ENST00000436817.6:c.1685A>G	ENSP00000415949.2:p.Lys562Arg
ENST00000493591.6:c.*1561A>G	ENSP00000494917.1:n.*1561A>G
ENST00000643399.2:c.1685A>G MANE Plus Clinical	ENSP00000494664.1:p.Lys562Arg
ENST00000298649.7:c.1670A>G	ENSP00000298649.3:p.Lys557Arg
ENST00000359426.6:c.1673A>G	ENSP00000352398.6:p.Lys558Arg
ENST00000360289.6:c.1637A>G	ENSP00000353433.2:p.Lys546Arg
ENST00000448642.6:c.1685A>G	ENSP00000402103.3:p.Lys562Arg
ENST00000494253.1:n.1899A>G
NM_000188.2:c.1673A>G	NP_000179.2:p.Lys558Arg
NM_033496.2:c.1670A>G	NP_277031.1:p.Lys557Arg
NM_033497.2:c.1685A>G	NP_277032.1:p.Lys562Arg
NM_033498.2:c.1685A>G	NP_277033.1:p.Lys562Arg
NM_033500.2:c.1637A>G , LRG_365t1:c.1637A>G	NP_277035.2:p.Lys546Arg
XM_005269735.2:c.1802A>G	XP_005269792.1:p.Lys601Arg
XM_005269736.1:c.1685A>G	XP_005269793.1:p.Lys562Arg
XM_005269737.1:c.1589A>G	XP_005269794.1:p.Lys530Arg
XM_011539732.1:c.1637A>G	XP_011538034.1:p.Lys546Arg
XM_011539733.1:c.1631A>G	XP_011538035.1:p.Lys544Arg
XM_011539734.1:c.1628A>G	XP_011538036.1:p.Lys543Arg
NM_001322364.1:c.1685A>G	NP_001309293.1:p.Lys562Arg
NM_001322365.1:c.1778A>G	NP_001309294.1:p.Lys593Arg
NM_001322366.1:c.1589A>G	NP_001309295.1:p.Lys530Arg
NM_001322367.1:c.1577A>G	NP_001309296.1:p.Lys526Arg
NM_001358263.1:c.1685A>G MANE Plus Clinical	NP_001345192.1:p.Lys562Arg
XM_024447969.1:c.1685A>G	XP_024303737.1:p.Lys562Arg
NM_000188.3:c.1673A>G MANE Select	NP_000179.2:p.Lys558Arg
NM_001322364.2:c.1685A>G	NP_001309293.1:p.Lys562Arg
NM_001322365.2:c.1778A>G	NP_001309294.1:p.Lys593Arg
NM_033496.3:c.1670A>G	NP_277031.1:p.Lys557Arg
NM_033497.3:c.1685A>G	NP_277032.1:p.Lys562Arg
NM_033498.3:c.1685A>G	NP_277033.1:p.Lys562Arg