Canonical Allele Identifier: CA376911365

Gene: HK1

Linked Data

• dbSNP Id: rs1446722078
• gnomAD v2: 10-71144188-A-G
• gnomAD v4: 10-69384432-A-G
• MyVariant Identifiers: chr10:g.71144188A>G (hg19) ; chr10:g.69384432A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69384432A>G , CM000672.2:g.69384432A>G	GRCh38
NC_000010.10:g.71144188A>G , CM000672.1:g.71144188A>G	GRCh37
NC_000010.9:g.70814194A>G	NCBI36
NG_012077.1:g.119433A>G , LRG_365:g.119433A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470050.2:c.1670A>G	ENSP00000515580.1:p.Asn557Ser
ENST00000703945.1:c.1586A>G	ENSP00000515578.1:p.Asn529Ser
ENST00000703946.1:c.1265+4337A>G	ENSP00000515579.1:n.1265+4337A>G
ENST00000703947.1:c.1280A>G	ENSP00000515581.1:p.Asn427Ser
ENST00000703948.1:c.*1287A>G	ENSP00000515582.1:n.*1287A>G
ENST00000703949.1:c.1670A>G	ENSP00000515583.1:p.Asn557Ser
ENST00000703950.1:c.1670A>G	ENSP00000515584.1:p.Asn557Ser
ENST00000703951.1:c.1265+4337A>G	ENSP00000515585.1:n.1265+4337A>G
ENST00000703952.1:c.1265+4337A>G	ENSP00000515586.1:n.1265+4337A>G
ENST00000703953.1:c.*933A>G	ENSP00000515587.1:n.*933A>G
ENST00000703954.1:c.1550A>G	ENSP00000515588.1:p.Asn517Ser
ENST00000703955.1:n.2220A>G
ENST00000703957.1:n.175A>G
ENST00000298649.8:c.1667A>G	ENSP00000298649.3:p.Asn556Ser
ENST00000359426.7:c.1670A>G MANE Select	ENSP00000352398.6:p.Asn557Ser
ENST00000436817.6:c.1682A>G	ENSP00000415949.2:p.Asn561Ser
ENST00000493591.6:c.*1558A>G	ENSP00000494917.1:n.*1558A>G
ENST00000643399.2:c.1682A>G MANE Plus Clinical	ENSP00000494664.1:p.Asn561Ser
ENST00000298649.7:c.1667A>G	ENSP00000298649.3:p.Asn556Ser
ENST00000359426.6:c.1670A>G	ENSP00000352398.6:p.Asn557Ser
ENST00000360289.6:c.1634A>G	ENSP00000353433.2:p.Asn545Ser
ENST00000448642.6:c.1682A>G	ENSP00000402103.3:p.Asn561Ser
ENST00000494253.1:n.1896A>G
NM_000188.2:c.1670A>G	NP_000179.2:p.Asn557Ser
NM_033496.2:c.1667A>G	NP_277031.1:p.Asn556Ser
NM_033497.2:c.1682A>G	NP_277032.1:p.Asn561Ser
NM_033498.2:c.1682A>G	NP_277033.1:p.Asn561Ser
NM_033500.2:c.1634A>G , LRG_365t1:c.1634A>G	NP_277035.2:p.Asn545Ser
XM_005269735.2:c.1799A>G	XP_005269792.1:p.Asn600Ser
XM_005269736.1:c.1682A>G	XP_005269793.1:p.Asn561Ser
XM_005269737.1:c.1586A>G	XP_005269794.1:p.Asn529Ser
XM_011539732.1:c.1634A>G	XP_011538034.1:p.Asn545Ser
XM_011539733.1:c.1628A>G	XP_011538035.1:p.Asn543Ser
XM_011539734.1:c.1625A>G	XP_011538036.1:p.Asn542Ser
NM_001322364.1:c.1682A>G	NP_001309293.1:p.Asn561Ser
NM_001322365.1:c.1775A>G	NP_001309294.1:p.Asn592Ser
NM_001322366.1:c.1586A>G	NP_001309295.1:p.Asn529Ser
NM_001322367.1:c.1574A>G	NP_001309296.1:p.Asn525Ser
NM_001358263.1:c.1682A>G MANE Plus Clinical	NP_001345192.1:p.Asn561Ser
XM_024447969.1:c.1682A>G	XP_024303737.1:p.Asn561Ser
NM_000188.3:c.1670A>G MANE Select	NP_000179.2:p.Asn557Ser
NM_001322364.2:c.1682A>G	NP_001309293.1:p.Asn561Ser
NM_001322365.2:c.1775A>G	NP_001309294.1:p.Asn592Ser
NM_033496.3:c.1667A>G	NP_277031.1:p.Asn556Ser
NM_033497.3:c.1682A>G	NP_277032.1:p.Asn561Ser
NM_033498.3:c.1682A>G	NP_277033.1:p.Asn561Ser