Canonical Allele Identifier: CA209224409

Gene: HK1

Linked Data

• dbSNP Id: rs769443773
• MyVariant Identifiers: chr10:g.71099846C>T (hg19) ; chr10:g.69340090C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69340090C>T , CM000672.2:g.69340090C>T	GRCh38
NC_000010.10:g.71099846C>T , CM000672.1:g.71099846C>T	GRCh37
NC_000010.9:g.70769852C>T	NCBI36
NG_012077.1:g.75091C>T , LRG_365:g.75091C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000470050.2:c.64-3737C>T	ENSP00000515580.1:n.64-3737C>T
ENST00000703944.1:c.76-3737C>T	ENSP00000515576.1:n.76-3737C>T
ENST00000703945.1:c.-21-3737C>T	ENSP00000515578.1:n.-21-3737C>T
ENST00000703946.1:c.64-3737C>T	ENSP00000515579.1:n.64-3737C>T
ENST00000703947.1:c.64-3737C>T	ENSP00000515581.1:n.64-3737C>T
ENST00000703948.1:c.64-3737C>T	ENSP00000515582.1:n.64-3737C>T
ENST00000703949.1:c.64-3737C>T	ENSP00000515583.1:n.64-3737C>T
ENST00000703950.1:c.64-3737C>T	ENSP00000515584.1:n.64-3737C>T
ENST00000703951.1:c.64-3737C>T	ENSP00000515585.1:n.64-3737C>T
ENST00000703952.1:c.64-3737C>T	ENSP00000515586.1:n.64-3737C>T
ENST00000703953.1:c.64-3737C>T	ENSP00000515587.1:n.64-3737C>T
ENST00000703954.1:c.64-3737C>T	ENSP00000515588.1:n.64-3737C>T
ENST00000703955.1:n.613+1414C>T
ENST00000298649.8:c.61-3737C>T	ENSP00000298649.3:n.61-3737C>T
ENST00000359426.7:c.64-3737C>T MANE Select	ENSP00000352398.6:n.64-3737C>T
ENST00000436817.6:c.76-3737C>T	ENSP00000415949.2:n.76-3737C>T
ENST00000450646.6:c.76-3737C>T	ENSP00000409761.2:n.76-3737C>T
ENST00000464803.6:c.169-3737C>T	ENSP00000496531.1:n.169-3737C>T
ENST00000476368.6:c.76-3737C>T	ENSP00000495526.1:n.76-3737C>T
ENST00000493591.6:c.231-3737C>T	ENSP00000494917.1:n.231-3737C>T
ENST00000643399.2:c.76-3737C>T MANE Plus Clinical	ENSP00000494664.1:n.76-3737C>T
ENST00000298649.7:c.61-3737C>T	ENSP00000298649.3:n.61-3737C>T
ENST00000359426.6:c.64-3737C>T	ENSP00000352398.6:n.64-3737C>T
ENST00000360289.6:c.28-3737C>T	ENSP00000353433.2:n.28-3737C>T
ENST00000421088.5:c.28-3737C>T	ENSP00000398316.1:n.28-3737C>T
ENST00000436817.5:c.61-3737C>T	ENSP00000415949.1:n.61-3737C>T
ENST00000448642.6:c.76-3737C>T	ENSP00000402103.3:n.76-3737C>T
ENST00000450646.5:c.76-3737C>T	ENSP00000409761.1:n.76-3737C>T
ENST00000464803.5:n.434-3737C>T
ENST00000476368.5:n.443-3737C>T
ENST00000480047.5:n.558+1414C>T
ENST00000483054.5:n.529-3737C>T
ENST00000483077.5:n.468-3737C>T
ENST00000493591.5:n.68-3737C>T
ENST00000494253.1:n.289+1782C>T
NM_000188.2:c.64-3737C>T	NP_000179.2:n.64-3737C>T
NM_033496.2:c.61-3737C>T	NP_277031.1:n.61-3737C>T
NM_033497.2:c.76-3737C>T	NP_277032.1:n.76-3737C>T
NM_033498.2:c.76-3737C>T	NP_277033.1:n.76-3737C>T
NM_033500.2:c.28-3737C>T , LRG_365t1:c.28-3737C>T	NP_277035.2:n.28-3737C>T
XM_005269735.2:c.193-3737C>T	XP_005269792.1:n.193-3737C>T
XM_005269736.1:c.76-3737C>T	XP_005269793.1:n.76-3737C>T
XM_005269737.1:c.-22+1414C>T	XP_005269794.1:n.-22+1414C>T
XM_011539732.1:c.28-3737C>T	XP_011538034.1:n.28-3737C>T
XM_011539733.1:c.22-3737C>T	XP_011538035.1:n.22-3737C>T
XM_011539734.1:c.19-3737C>T	XP_011538036.1:n.19-3737C>T
NM_001322364.1:c.76-3737C>T	NP_001309293.1:n.76-3737C>T
NM_001322365.1:c.169-3737C>T	NP_001309294.1:n.169-3737C>T
NM_001322366.1:c.-21-3737C>T	NP_001309295.1:n.-21-3737C>T
NM_001322367.1:c.64-3737C>T	NP_001309296.1:n.64-3737C>T
NM_001358263.1:c.76-3737C>T MANE Plus Clinical	NP_001345192.1:n.76-3737C>T
XM_024447969.1:c.76-3737C>T	XP_024303737.1:n.76-3737C>T
NM_000188.3:c.64-3737C>T MANE Select	NP_000179.2:n.64-3737C>T
NM_001322364.2:c.76-3737C>T	NP_001309293.1:n.76-3737C>T
NM_001322365.2:c.169-3737C>T	NP_001309294.1:n.169-3737C>T
NM_033496.3:c.61-3737C>T	NP_277031.1:n.61-3737C>T
NM_033497.3:c.76-3737C>T	NP_277032.1:n.76-3737C>T
NM_033498.3:c.76-3737C>T	NP_277033.1:n.76-3737C>T