Canonical Allele Identifier: CA376909565

Gene: HK1

Linked Data

• MyVariant Identifiers: chr10:g.71142277T>A (hg19) ; chr10:g.69382521T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69382521T>A , CM000672.2:g.69382521T>A	GRCh38
NC_000010.10:g.71142277T>A , CM000672.1:g.71142277T>A	GRCh37
NC_000010.9:g.70812283T>A	NCBI36
NG_012077.1:g.117522T>A , LRG_365:g.117522T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470050.2:c.1300T>A	ENSP00000515580.1:p.Leu434Met
ENST00000703945.1:c.1216T>A	ENSP00000515578.1:p.Leu406Met
ENST00000703946.1:c.1265+2426T>A	ENSP00000515579.1:n.1265+2426T>A
ENST00000703947.1:c.910T>A	ENSP00000515581.1:p.Leu304Met
ENST00000703948.1:c.*917T>A	ENSP00000515582.1:n.*917T>A
ENST00000703949.1:c.1300T>A	ENSP00000515583.1:p.Leu434Met
ENST00000703950.1:c.1300T>A	ENSP00000515584.1:p.Leu434Met
ENST00000703951.1:c.1265+2426T>A	ENSP00000515585.1:n.1265+2426T>A
ENST00000703952.1:c.1265+2426T>A	ENSP00000515586.1:n.1265+2426T>A
ENST00000703953.1:c.*563T>A	ENSP00000515587.1:n.*563T>A
ENST00000703954.1:c.1180T>A	ENSP00000515588.1:p.Leu394Met
ENST00000703955.1:n.1850T>A
ENST00000298649.8:c.1297T>A	ENSP00000298649.3:p.Leu433Met
ENST00000359426.7:c.1300T>A MANE Select	ENSP00000352398.6:p.Leu434Met
ENST00000436817.6:c.1312T>A	ENSP00000415949.2:p.Leu438Met
ENST00000493591.6:c.*1188T>A	ENSP00000494917.1:n.*1188T>A
ENST00000643399.2:c.1312T>A MANE Plus Clinical	ENSP00000494664.1:p.Leu438Met
ENST00000298649.7:c.1297T>A	ENSP00000298649.3:p.Leu433Met
ENST00000359426.6:c.1300T>A	ENSP00000352398.6:p.Leu434Met
ENST00000360289.6:c.1264T>A	ENSP00000353433.2:p.Leu422Met
ENST00000448642.6:c.1312T>A	ENSP00000402103.3:p.Leu438Met
ENST00000494253.1:n.1526T>A
NM_000188.2:c.1300T>A	NP_000179.2:p.Leu434Met
NM_033496.2:c.1297T>A	NP_277031.1:p.Leu433Met
NM_033497.2:c.1312T>A	NP_277032.1:p.Leu438Met
NM_033498.2:c.1312T>A	NP_277033.1:p.Leu438Met
NM_033500.2:c.1264T>A , LRG_365t1:c.1264T>A	NP_277035.2:p.Leu422Met
XM_005269735.2:c.1429T>A	XP_005269792.1:p.Leu477Met
XM_005269736.1:c.1312T>A	XP_005269793.1:p.Leu438Met
XM_005269737.1:c.1216T>A	XP_005269794.1:p.Leu406Met
XM_011539732.1:c.1264T>A	XP_011538034.1:p.Leu422Met
XM_011539733.1:c.1258T>A	XP_011538035.1:p.Leu420Met
XM_011539734.1:c.1255T>A	XP_011538036.1:p.Leu419Met
NM_001322364.1:c.1312T>A	NP_001309293.1:p.Leu438Met
NM_001322365.1:c.1405T>A	NP_001309294.1:p.Leu469Met
NM_001322366.1:c.1216T>A	NP_001309295.1:p.Leu406Met
NM_001322367.1:c.1204T>A	NP_001309296.1:p.Leu402Met
NM_001358263.1:c.1312T>A MANE Plus Clinical	NP_001345192.1:p.Leu438Met
XM_024447969.1:c.1312T>A	XP_024303737.1:p.Leu438Met
NM_000188.3:c.1300T>A MANE Select	NP_000179.2:p.Leu434Met
NM_001322364.2:c.1312T>A	NP_001309293.1:p.Leu438Met
NM_001322365.2:c.1405T>A	NP_001309294.1:p.Leu469Met
NM_033496.3:c.1297T>A	NP_277031.1:p.Leu433Met
NM_033497.3:c.1312T>A	NP_277032.1:p.Leu438Met
NM_033498.3:c.1312T>A	NP_277033.1:p.Leu438Met