Canonical Allele Identifier: CA2832560399

Gene: HK1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69382578dup , CM000672.2:g.69382578dup	GRCh38
NC_000010.10:g.71142334dup , CM000672.1:g.71142334dup	GRCh37
NC_000010.9:g.70812340dup	NCBI36
NG_012077.1:g.117579dup , LRG_365:g.117579dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470050.2:c.1357dup	ENSP00000515580.1:p.Ala453GlyfsTer?
ENST00000703945.1:c.1273dup	ENSP00000515578.1:p.Ala425GlyfsTer?
ENST00000703946.1:c.1265+2483dup	ENSP00000515579.1:n.1265+2483dup
ENST00000703947.1:c.967dup	ENSP00000515581.1:p.Ala323GlyfsTer?
ENST00000703948.1:c.*974dup	ENSP00000515582.1:n.*974dup
ENST00000703949.1:c.1357dup	ENSP00000515583.1:p.Ala453GlyfsTer?
ENST00000703950.1:c.1357dup	ENSP00000515584.1:p.Ala453GlyfsTer?
ENST00000703951.1:c.1265+2483dup	ENSP00000515585.1:n.1265+2483dup
ENST00000703952.1:c.1265+2483dup	ENSP00000515586.1:n.1265+2483dup
ENST00000703953.1:c.*620dup	ENSP00000515587.1:n.*620dup
ENST00000703954.1:c.1237dup	ENSP00000515588.1:p.Ala413GlyfsTer?
ENST00000703955.1:n.1907dup
ENST00000298649.8:c.1354dup	ENSP00000298649.3:p.Ala452GlyfsTer?
ENST00000359426.7:c.1357dup MANE Select	ENSP00000352398.6:p.Ala453GlyfsTer?
ENST00000436817.6:c.1369dup	ENSP00000415949.2:p.Ala457GlyfsTer?
ENST00000493591.6:c.*1245dup	ENSP00000494917.1:n.*1245dup
ENST00000643399.2:c.1369dup MANE Plus Clinical	ENSP00000494664.1:p.Ala457GlyfsTer?
ENST00000298649.7:c.1354dup	ENSP00000298649.3:p.Ala452GlyfsTer?
ENST00000359426.6:c.1357dup	ENSP00000352398.6:p.Ala453GlyfsTer?
ENST00000360289.6:c.1321dup	ENSP00000353433.2:p.Ala441GlyfsTer?
ENST00000448642.6:c.1369dup	ENSP00000402103.3:p.Ala457GlyfsTer?
ENST00000494253.1:n.1583dup
NM_000188.2:c.1357dup	NP_000179.2:p.Ala453GlyfsTer?
NM_033496.2:c.1354dup	NP_277031.1:p.Ala452GlyfsTer?
NM_033497.2:c.1369dup	NP_277032.1:p.Ala457GlyfsTer?
NM_033498.2:c.1369dup	NP_277033.1:p.Ala457GlyfsTer?
NM_033500.2:c.1321dup , LRG_365t1:c.1321dup	NP_277035.2:p.Ala441GlyfsTer?
XM_005269735.2:c.1486dup	XP_005269792.1:p.Ala496GlyfsTer?
XM_005269736.1:c.1369dup	XP_005269793.1:p.Ala457GlyfsTer?
XM_005269737.1:c.1273dup	XP_005269794.1:p.Ala425GlyfsTer?
XM_011539732.1:c.1321dup	XP_011538034.1:p.Ala441GlyfsTer?
XM_011539733.1:c.1315dup	XP_011538035.1:p.Ala439GlyfsTer?
XM_011539734.1:c.1312dup	XP_011538036.1:p.Ala438GlyfsTer?
NM_001322364.1:c.1369dup	NP_001309293.1:p.Ala457GlyfsTer?
NM_001322365.1:c.1462dup	NP_001309294.1:p.Ala488GlyfsTer?
NM_001322366.1:c.1273dup	NP_001309295.1:p.Ala425GlyfsTer?
NM_001322367.1:c.1261dup	NP_001309296.1:p.Ala421GlyfsTer?
NM_001358263.1:c.1369dup MANE Plus Clinical	NP_001345192.1:p.Ala457GlyfsTer?
XM_024447969.1:c.1369dup	XP_024303737.1:p.Ala457GlyfsTer?
NM_000188.3:c.1357dup MANE Select	NP_000179.2:p.Ala453GlyfsTer?
NM_001322364.2:c.1369dup	NP_001309293.1:p.Ala457GlyfsTer?
NM_001322365.2:c.1462dup	NP_001309294.1:p.Ala488GlyfsTer?
NM_033496.3:c.1354dup	NP_277031.1:p.Ala452GlyfsTer?
NM_033497.3:c.1369dup	NP_277032.1:p.Ala457GlyfsTer?
NM_033498.3:c.1369dup	NP_277033.1:p.Ala457GlyfsTer?