Canonical Allele Identifier: CA5532592

Gene: HK1

Linked Data

• ClinVar Variation Id: 915369
• ClinVar RCV Id: RCV001169973
• dbSNP Id: rs780576140
• ExAC: 10:71142370 G / A
• gnomAD v2: 10-71142370-G-A
• gnomAD v3: 10-69382614-G-A
• gnomAD v4: 10-69382614-G-A
• MyVariant Identifiers: chr10:g.71142370G>A (hg19) ; chr10:g.69382614G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69382614G>A , CM000672.2:g.69382614G>A	GRCh38
NC_000010.10:g.71142370G>A , CM000672.1:g.71142370G>A	GRCh37
NC_000010.9:g.70812376G>A	NCBI36
NG_012077.1:g.117615G>A , LRG_365:g.117615G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000470050.2:c.1393G>A	ENSP00000515580.1:p.Glu465Lys
ENST00000703945.1:c.1309G>A	ENSP00000515578.1:p.Glu437Lys
ENST00000703946.1:c.1265+2519G>A	ENSP00000515579.1:n.1265+2519G>A
ENST00000703947.1:c.1003G>A	ENSP00000515581.1:p.Glu335Lys
ENST00000703948.1:c.*1010G>A	ENSP00000515582.1:n.*1010G>A
ENST00000703949.1:c.1393G>A	ENSP00000515583.1:p.Glu465Lys
ENST00000703950.1:c.1393G>A	ENSP00000515584.1:p.Glu465Lys
ENST00000703951.1:c.1265+2519G>A	ENSP00000515585.1:n.1265+2519G>A
ENST00000703952.1:c.1265+2519G>A	ENSP00000515586.1:n.1265+2519G>A
ENST00000703953.1:c.*656G>A	ENSP00000515587.1:n.*656G>A
ENST00000703954.1:c.1273G>A	ENSP00000515588.1:p.Glu425Lys
ENST00000703955.1:n.1943G>A
ENST00000298649.8:c.1390G>A	ENSP00000298649.3:p.Glu464Lys
ENST00000359426.7:c.1393G>A MANE Select	ENSP00000352398.6:p.Glu465Lys
ENST00000436817.6:c.1405G>A	ENSP00000415949.2:p.Glu469Lys
ENST00000493591.6:c.*1281G>A	ENSP00000494917.1:n.*1281G>A
ENST00000643399.2:c.1405G>A MANE Plus Clinical	ENSP00000494664.1:p.Glu469Lys
ENST00000298649.7:c.1390G>A	ENSP00000298649.3:p.Glu464Lys
ENST00000359426.6:c.1393G>A	ENSP00000352398.6:p.Glu465Lys
ENST00000360289.6:c.1357G>A	ENSP00000353433.2:p.Glu453Lys
ENST00000448642.6:c.1405G>A	ENSP00000402103.3:p.Glu469Lys
ENST00000494253.1:n.1619G>A
NM_000188.2:c.1393G>A	NP_000179.2:p.Glu465Lys
NM_033496.2:c.1390G>A	NP_277031.1:p.Glu464Lys
NM_033497.2:c.1405G>A	NP_277032.1:p.Glu469Lys
NM_033498.2:c.1405G>A	NP_277033.1:p.Glu469Lys
NM_033500.2:c.1357G>A , LRG_365t1:c.1357G>A	NP_277035.2:p.Glu453Lys
XM_005269735.2:c.1522G>A	XP_005269792.1:p.Glu508Lys
XM_005269736.1:c.1405G>A	XP_005269793.1:p.Glu469Lys
XM_005269737.1:c.1309G>A	XP_005269794.1:p.Glu437Lys
XM_011539732.1:c.1357G>A	XP_011538034.1:p.Glu453Lys
XM_011539733.1:c.1351G>A	XP_011538035.1:p.Glu451Lys
XM_011539734.1:c.1348G>A	XP_011538036.1:p.Glu450Lys
NM_001322364.1:c.1405G>A	NP_001309293.1:p.Glu469Lys
NM_001322365.1:c.1498G>A	NP_001309294.1:p.Glu500Lys
NM_001322366.1:c.1309G>A	NP_001309295.1:p.Glu437Lys
NM_001322367.1:c.1297G>A	NP_001309296.1:p.Glu433Lys
NM_001358263.1:c.1405G>A MANE Plus Clinical	NP_001345192.1:p.Glu469Lys
XM_024447969.1:c.1405G>A	XP_024303737.1:p.Glu469Lys
NM_000188.3:c.1393G>A MANE Select	NP_000179.2:p.Glu465Lys
NM_001322364.2:c.1405G>A	NP_001309293.1:p.Glu469Lys
NM_001322365.2:c.1498G>A	NP_001309294.1:p.Glu500Lys
NM_033496.3:c.1390G>A	NP_277031.1:p.Glu464Lys
NM_033497.3:c.1405G>A	NP_277032.1:p.Glu469Lys
NM_033498.3:c.1405G>A	NP_277033.1:p.Glu469Lys