Canonical Allele Identifier: CA2499220305

Gene: HK1

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69319018C>T , CM000672.2:g.69319018C>T	GRCh38
NC_000010.10:g.71078774C>T , CM000672.1:g.71078774C>T	GRCh37
NC_000010.9:g.70748780C>T	NCBI36
NG_012077.1:g.54019C>T , LRG_365:g.54019C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470050.2:c.63+8C>T	ENSP00000515580.1:n.63+8C>T
ENST00000703944.1:c.75+23338C>T	ENSP00000515576.1:n.75+23338C>T
ENST00000703945.1:c.-22+783C>T	ENSP00000515578.1:n.-22+783C>T
ENST00000703946.1:c.63+8C>T	ENSP00000515579.1:n.63+8C>T
ENST00000703947.1:c.63+8C>T	ENSP00000515581.1:n.63+8C>T
ENST00000703948.1:c.63+8C>T	ENSP00000515582.1:n.63+8C>T
ENST00000703949.1:c.63+8C>T	ENSP00000515583.1:n.63+8C>T
ENST00000703950.1:c.63+8C>T	ENSP00000515584.1:n.63+8C>T
ENST00000703951.1:c.63+8C>T	ENSP00000515585.1:n.63+8C>T
ENST00000703952.1:c.63+8C>T	ENSP00000515586.1:n.63+8C>T
ENST00000703953.1:c.63+8C>T	ENSP00000515587.1:n.63+8C>T
ENST00000703954.1:c.63+8C>T	ENSP00000515588.1:n.63+8C>T
ENST00000298649.8:c.60+3004C>T	ENSP00000298649.3:n.60+3004C>T
ENST00000359426.7:c.63+8C>T MANE Select	ENSP00000352398.6:n.63+8C>T
ENST00000436817.6:c.75+23338C>T	ENSP00000415949.2:n.75+23338C>T
ENST00000450646.6:c.75+23338C>T	ENSP00000409761.2:n.75+23338C>T
ENST00000464803.6:c.168+23338C>T	ENSP00000496531.1:n.168+23338C>T
ENST00000476368.6:c.75+23338C>T	ENSP00000495526.1:n.75+23338C>T
ENST00000493591.6:c.71C>T	ENSP00000494917.1:p.Pro24Leu
ENST00000643399.2:c.75+23338C>T MANE Plus Clinical	ENSP00000494664.1:n.75+23338C>T
ENST00000298649.7:c.60+3004C>T	ENSP00000298649.3:n.60+3004C>T
ENST00000359426.6:c.63+8C>T	ENSP00000352398.6:n.63+8C>T
ENST00000360289.6:c.27+18157C>T	ENSP00000353433.2:n.27+18157C>T
ENST00000421088.5:c.27+18157C>T	ENSP00000398316.1:n.27+18157C>T
ENST00000436817.5:c.60+3004C>T	ENSP00000415949.1:n.60+3004C>T
ENST00000448642.6:c.75+23338C>T	ENSP00000402103.3:n.75+23338C>T
ENST00000450646.5:c.75+23338C>T	ENSP00000409761.1:n.75+23338C>T
ENST00000464803.5:n.433+23338C>T
ENST00000476368.5:n.442+23338C>T
ENST00000480047.5:n.380-19480C>T
ENST00000483054.5:n.528+23338C>T
ENST00000483077.5:n.467+18157C>T
NM_000188.2:c.63+8C>T	NP_000179.2:n.63+8C>T
NM_033496.2:c.60+3004C>T	NP_277031.1:n.60+3004C>T
NM_033497.2:c.75+23338C>T	NP_277032.1:n.75+23338C>T
NM_033498.2:c.75+23338C>T	NP_277033.1:n.75+23338C>T
NM_033500.2:c.27+18157C>T , LRG_365t1:c.27+18157C>T	NP_277035.2:n.27+18157C>T
XM_005269735.2:c.192+783C>T	XP_005269792.1:n.192+783C>T
XM_005269736.1:c.75+23338C>T	XP_005269793.1:n.75+23338C>T
XM_011539732.1:c.27+18157C>T	XP_011538034.1:n.27+18157C>T
NM_001322364.1:c.75+23338C>T	NP_001309293.1:n.75+23338C>T
NM_001322365.1:c.168+23338C>T	NP_001309294.1:n.168+23338C>T
NM_001322366.1:c.-22+783C>T	NP_001309295.1:n.-22+783C>T
NM_001322367.1:c.63+8C>T	NP_001309296.1:n.63+8C>T
NM_001358263.1:c.75+23338C>T MANE Plus Clinical	NP_001345192.1:n.75+23338C>T
XM_024447969.1:c.75+23338C>T	XP_024303737.1:n.75+23338C>T
NM_000188.3:c.63+8C>T MANE Select	NP_000179.2:n.63+8C>T
NM_001322364.2:c.75+23338C>T	NP_001309293.1:n.75+23338C>T
NM_001322365.2:c.168+23338C>T	NP_001309294.1:n.168+23338C>T
NM_033496.3:c.60+3004C>T	NP_277031.1:n.60+3004C>T
NM_033497.3:c.75+23338C>T	NP_277032.1:n.75+23338C>T
NM_033498.3:c.75+23338C>T	NP_277033.1:n.75+23338C>T