Canonical Allele Identifier: CA376911411

Gene: HK1

Linked Data

• MyVariant Identifiers: chr10:g.71144208A>T (hg19) ; chr10:g.69384452A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69384452A>T , CM000672.2:g.69384452A>T	GRCh38
NC_000010.10:g.71144208A>T , CM000672.1:g.71144208A>T	GRCh37
NC_000010.9:g.70814214A>T	NCBI36
NG_012077.1:g.119453A>T , LRG_365:g.119453A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470050.2:c.1690A>T	ENSP00000515580.1:p.Ile564Phe
ENST00000703945.1:c.1606A>T	ENSP00000515578.1:p.Ile536Phe
ENST00000703946.1:c.1265+4357A>T	ENSP00000515579.1:n.1265+4357A>T
ENST00000703947.1:c.1300A>T	ENSP00000515581.1:p.Ile434Phe
ENST00000703948.1:c.*1307A>T	ENSP00000515582.1:n.*1307A>T
ENST00000703949.1:c.1690A>T	ENSP00000515583.1:p.Ile564Phe
ENST00000703950.1:c.1690A>T	ENSP00000515584.1:p.Ile564Phe
ENST00000703951.1:c.1265+4357A>T	ENSP00000515585.1:n.1265+4357A>T
ENST00000703952.1:c.1265+4357A>T	ENSP00000515586.1:n.1265+4357A>T
ENST00000703953.1:c.*953A>T	ENSP00000515587.1:n.*953A>T
ENST00000703954.1:c.1570A>T	ENSP00000515588.1:p.Ile524Phe
ENST00000703955.1:n.2240A>T
ENST00000703957.1:n.195A>T
ENST00000298649.8:c.1687A>T	ENSP00000298649.3:p.Ile563Phe
ENST00000359426.7:c.1690A>T MANE Select	ENSP00000352398.6:p.Ile564Phe
ENST00000436817.6:c.1702A>T	ENSP00000415949.2:p.Ile568Phe
ENST00000493591.6:c.*1578A>T	ENSP00000494917.1:n.*1578A>T
ENST00000643399.2:c.1702A>T MANE Plus Clinical	ENSP00000494664.1:p.Ile568Phe
ENST00000298649.7:c.1687A>T	ENSP00000298649.3:p.Ile563Phe
ENST00000359426.6:c.1690A>T	ENSP00000352398.6:p.Ile564Phe
ENST00000360289.6:c.1654A>T	ENSP00000353433.2:p.Ile552Phe
ENST00000448642.6:c.1702A>T	ENSP00000402103.3:p.Ile568Phe
ENST00000494253.1:n.1916A>T
NM_000188.2:c.1690A>T	NP_000179.2:p.Ile564Phe
NM_033496.2:c.1687A>T	NP_277031.1:p.Ile563Phe
NM_033497.2:c.1702A>T	NP_277032.1:p.Ile568Phe
NM_033498.2:c.1702A>T	NP_277033.1:p.Ile568Phe
NM_033500.2:c.1654A>T , LRG_365t1:c.1654A>T	NP_277035.2:p.Ile552Phe
XM_005269735.2:c.1819A>T	XP_005269792.1:p.Ile607Phe
XM_005269736.1:c.1702A>T	XP_005269793.1:p.Ile568Phe
XM_005269737.1:c.1606A>T	XP_005269794.1:p.Ile536Phe
XM_011539732.1:c.1654A>T	XP_011538034.1:p.Ile552Phe
XM_011539733.1:c.1648A>T	XP_011538035.1:p.Ile550Phe
XM_011539734.1:c.1645A>T	XP_011538036.1:p.Ile549Phe
NM_001322364.1:c.1702A>T	NP_001309293.1:p.Ile568Phe
NM_001322365.1:c.1795A>T	NP_001309294.1:p.Ile599Phe
NM_001322366.1:c.1606A>T	NP_001309295.1:p.Ile536Phe
NM_001322367.1:c.1594A>T	NP_001309296.1:p.Ile532Phe
NM_001358263.1:c.1702A>T MANE Plus Clinical	NP_001345192.1:p.Ile568Phe
XM_024447969.1:c.1702A>T	XP_024303737.1:p.Ile568Phe
NM_000188.3:c.1690A>T MANE Select	NP_000179.2:p.Ile564Phe
NM_001322364.2:c.1702A>T	NP_001309293.1:p.Ile568Phe
NM_001322365.2:c.1795A>T	NP_001309294.1:p.Ile599Phe
NM_033496.3:c.1687A>T	NP_277031.1:p.Ile563Phe
NM_033497.3:c.1702A>T	NP_277032.1:p.Ile568Phe
NM_033498.3:c.1702A>T	NP_277033.1:p.Ile568Phe