Canonical Allele Identifier: CA470027318

Gene: HK1

Linked Data

• MyVariant Identifiers: chr10:g.71144225C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69384469C>T , CM000672.2:g.69384469C>T	GRCh38
NC_000010.10:g.71144225C>T , CM000672.1:g.71144225C>T	GRCh37
NC_000010.9:g.70814231C>T	NCBI36
NG_012077.1:g.119470C>T , LRG_365:g.119470C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470050.2:c.1707C>T	ENSP00000515580.1:p.Gly569=
ENST00000703945.1:c.1623C>T	ENSP00000515578.1:p.Gly541=
ENST00000703946.1:c.1265+4374C>T	ENSP00000515579.1:n.1265+4374C>T
ENST00000703947.1:c.1317C>T	ENSP00000515581.1:p.Gly439=
ENST00000703948.1:c.*1324C>T	ENSP00000515582.1:n.*1324C>T
ENST00000703949.1:c.1707C>T	ENSP00000515583.1:p.Gly569=
ENST00000703950.1:c.1707C>T	ENSP00000515584.1:p.Gly569=
ENST00000703951.1:c.1265+4374C>T	ENSP00000515585.1:n.1265+4374C>T
ENST00000703952.1:c.1265+4374C>T	ENSP00000515586.1:n.1265+4374C>T
ENST00000703953.1:c.*970C>T	ENSP00000515587.1:n.*970C>T
ENST00000703954.1:c.1587C>T	ENSP00000515588.1:p.Gly529=
ENST00000703955.1:n.2257C>T
ENST00000703957.1:n.212C>T
ENST00000298649.8:c.1704C>T	ENSP00000298649.3:p.Gly568=
ENST00000359426.7:c.1707C>T MANE Select	ENSP00000352398.6:p.Gly569=
ENST00000436817.6:c.1719C>T	ENSP00000415949.2:p.Gly573=
ENST00000493591.6:c.*1595C>T	ENSP00000494917.1:n.*1595C>T
ENST00000643399.2:c.1719C>T MANE Plus Clinical	ENSP00000494664.1:p.Gly573=
ENST00000298649.7:c.1704C>T	ENSP00000298649.3:p.Gly568=
ENST00000359426.6:c.1707C>T	ENSP00000352398.6:p.Gly569=
ENST00000360289.6:c.1671C>T	ENSP00000353433.2:p.Gly557=
ENST00000448642.6:c.1719C>T	ENSP00000402103.3:p.Gly573=
ENST00000494253.1:n.1933C>T
NM_000188.2:c.1707C>T	NP_000179.2:p.Gly569=
NM_033496.2:c.1704C>T	NP_277031.1:p.Gly568=
NM_033497.2:c.1719C>T	NP_277032.1:p.Gly573=
NM_033498.2:c.1719C>T	NP_277033.1:p.Gly573=
NM_033500.2:c.1671C>T , LRG_365t1:c.1671C>T	NP_277035.2:p.Gly557=
XM_005269735.2:c.1836C>T	XP_005269792.1:p.Gly612=
XM_005269736.1:c.1719C>T	XP_005269793.1:p.Gly573=
XM_005269737.1:c.1623C>T	XP_005269794.1:p.Gly541=
XM_011539732.1:c.1671C>T	XP_011538034.1:p.Gly557=
XM_011539733.1:c.1665C>T	XP_011538035.1:p.Gly555=
XM_011539734.1:c.1662C>T	XP_011538036.1:p.Gly554=
NM_001322364.1:c.1719C>T	NP_001309293.1:p.Gly573=
NM_001322365.1:c.1812C>T	NP_001309294.1:p.Gly604=
NM_001322366.1:c.1623C>T	NP_001309295.1:p.Gly541=
NM_001322367.1:c.1611C>T	NP_001309296.1:p.Gly537=
NM_001358263.1:c.1719C>T MANE Plus Clinical	NP_001345192.1:p.Gly573=
XM_024447969.1:c.1719C>T	XP_024303737.1:p.Gly573=
NM_000188.3:c.1707C>T MANE Select	NP_000179.2:p.Gly569=
NM_001322364.2:c.1719C>T	NP_001309293.1:p.Gly573=
NM_001322365.2:c.1812C>T	NP_001309294.1:p.Gly604=
NM_033496.3:c.1704C>T	NP_277031.1:p.Gly568=
NM_033497.3:c.1719C>T	NP_277032.1:p.Gly573=
NM_033498.3:c.1719C>T	NP_277033.1:p.Gly573=