Canonical Allele Identifier: CA667891629

Gene: HK1

Linked Data

• dbSNP Id: rs1236942049
• MyVariant Identifiers: chr10:g.71099872T>G (hg19) ; chr10:g.69340116T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69340116T>G , CM000672.2:g.69340116T>G	GRCh38
NC_000010.10:g.71099872T>G , CM000672.1:g.71099872T>G	GRCh37
NC_000010.9:g.70769878T>G	NCBI36
NG_012077.1:g.75117T>G , LRG_365:g.75117T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000470050.2:c.64-3711T>G	ENSP00000515580.1:n.64-3711T>G
ENST00000703944.1:c.76-3711T>G	ENSP00000515576.1:n.76-3711T>G
ENST00000703945.1:c.-21-3711T>G	ENSP00000515578.1:n.-21-3711T>G
ENST00000703946.1:c.64-3711T>G	ENSP00000515579.1:n.64-3711T>G
ENST00000703947.1:c.64-3711T>G	ENSP00000515581.1:n.64-3711T>G
ENST00000703948.1:c.64-3711T>G	ENSP00000515582.1:n.64-3711T>G
ENST00000703949.1:c.64-3711T>G	ENSP00000515583.1:n.64-3711T>G
ENST00000703950.1:c.64-3711T>G	ENSP00000515584.1:n.64-3711T>G
ENST00000703951.1:c.64-3711T>G	ENSP00000515585.1:n.64-3711T>G
ENST00000703952.1:c.64-3711T>G	ENSP00000515586.1:n.64-3711T>G
ENST00000703953.1:c.64-3711T>G	ENSP00000515587.1:n.64-3711T>G
ENST00000703954.1:c.64-3711T>G	ENSP00000515588.1:n.64-3711T>G
ENST00000703955.1:n.613+1440T>G
ENST00000298649.8:c.61-3711T>G	ENSP00000298649.3:n.61-3711T>G
ENST00000359426.7:c.64-3711T>G MANE Select	ENSP00000352398.6:n.64-3711T>G
ENST00000436817.6:c.76-3711T>G	ENSP00000415949.2:n.76-3711T>G
ENST00000450646.6:c.76-3711T>G	ENSP00000409761.2:n.76-3711T>G
ENST00000464803.6:c.169-3711T>G	ENSP00000496531.1:n.169-3711T>G
ENST00000476368.6:c.76-3711T>G	ENSP00000495526.1:n.76-3711T>G
ENST00000493591.6:c.231-3711T>G	ENSP00000494917.1:n.231-3711T>G
ENST00000643399.2:c.76-3711T>G MANE Plus Clinical	ENSP00000494664.1:n.76-3711T>G
ENST00000298649.7:c.61-3711T>G	ENSP00000298649.3:n.61-3711T>G
ENST00000359426.6:c.64-3711T>G	ENSP00000352398.6:n.64-3711T>G
ENST00000360289.6:c.28-3711T>G	ENSP00000353433.2:n.28-3711T>G
ENST00000421088.5:c.28-3711T>G	ENSP00000398316.1:n.28-3711T>G
ENST00000436817.5:c.61-3711T>G	ENSP00000415949.1:n.61-3711T>G
ENST00000448642.6:c.76-3711T>G	ENSP00000402103.3:n.76-3711T>G
ENST00000450646.5:c.76-3711T>G	ENSP00000409761.1:n.76-3711T>G
ENST00000464803.5:n.434-3711T>G
ENST00000476368.5:n.443-3711T>G
ENST00000480047.5:n.558+1440T>G
ENST00000483054.5:n.529-3711T>G
ENST00000483077.5:n.468-3711T>G
ENST00000493591.5:n.68-3711T>G
ENST00000494253.1:n.289+1808T>G
NM_000188.2:c.64-3711T>G	NP_000179.2:n.64-3711T>G
NM_033496.2:c.61-3711T>G	NP_277031.1:n.61-3711T>G
NM_033497.2:c.76-3711T>G	NP_277032.1:n.76-3711T>G
NM_033498.2:c.76-3711T>G	NP_277033.1:n.76-3711T>G
NM_033500.2:c.28-3711T>G , LRG_365t1:c.28-3711T>G	NP_277035.2:n.28-3711T>G
XM_005269735.2:c.193-3711T>G	XP_005269792.1:n.193-3711T>G
XM_005269736.1:c.76-3711T>G	XP_005269793.1:n.76-3711T>G
XM_005269737.1:c.-22+1440T>G	XP_005269794.1:n.-22+1440T>G
XM_011539732.1:c.28-3711T>G	XP_011538034.1:n.28-3711T>G
XM_011539733.1:c.22-3711T>G	XP_011538035.1:n.22-3711T>G
XM_011539734.1:c.19-3711T>G	XP_011538036.1:n.19-3711T>G
NM_001322364.1:c.76-3711T>G	NP_001309293.1:n.76-3711T>G
NM_001322365.1:c.169-3711T>G	NP_001309294.1:n.169-3711T>G
NM_001322366.1:c.-21-3711T>G	NP_001309295.1:n.-21-3711T>G
NM_001322367.1:c.64-3711T>G	NP_001309296.1:n.64-3711T>G
NM_001358263.1:c.76-3711T>G MANE Plus Clinical	NP_001345192.1:n.76-3711T>G
XM_024447969.1:c.76-3711T>G	XP_024303737.1:n.76-3711T>G
NM_000188.3:c.64-3711T>G MANE Select	NP_000179.2:n.64-3711T>G
NM_001322364.2:c.76-3711T>G	NP_001309293.1:n.76-3711T>G
NM_001322365.2:c.169-3711T>G	NP_001309294.1:n.169-3711T>G
NM_033496.3:c.61-3711T>G	NP_277031.1:n.61-3711T>G
NM_033497.3:c.76-3711T>G	NP_277032.1:n.76-3711T>G
NM_033498.3:c.76-3711T>G	NP_277033.1:n.76-3711T>G