Canonical Allele Identifier: CA1917773056

Gene: HK1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69384160_69384163delinsTGTG , CM000672.2:g.69384160_69384163delinsTGTG	GRCh38
NC_000010.10:g.71143916_71143919delinsTGTG , CM000672.1:g.71143916_71143919delinsTGTG	GRCh37
NC_000010.9:g.70813922_70813925delinsTGTG	NCBI36
NG_012077.1:g.119161_119164delinsTGTG , LRG_365:g.119161_119164delinsTGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470050.2:c.1571-173_1571-170delinsTGTG	ENSP00000515580.1:n.1571-173_1571-170delinsTGTG
ENST00000703945.1:c.1487-173_1487-170delinsTGTG	ENSP00000515578.1:n.1487-173_1487-170delinsTGTG
ENST00000703946.1:c.1265+4065_1265+4068delinsTGTG	ENSP00000515579.1:n.1265+4065_1265+4068delinsTGTG
ENST00000703947.1:c.1181-173_1181-170delinsTGTG	ENSP00000515581.1:n.1181-173_1181-170delinsTGTG
ENST00000703948.1:c.*1188-173_*1188-170delinsTGTG	ENSP00000515582.1:n.*1188-173_*1188-170delinsTGTG
ENST00000703949.1:c.1571-173_1571-170delinsTGTG	ENSP00000515583.1:n.1571-173_1571-170delinsTGTG
ENST00000703950.1:c.1571-173_1571-170delinsTGTG	ENSP00000515584.1:n.1571-173_1571-170delinsTGTG
ENST00000703951.1:c.1265+4065_1265+4068delinsTGTG	ENSP00000515585.1:n.1265+4065_1265+4068delinsTGTG
ENST00000703952.1:c.1265+4065_1265+4068delinsTGTG	ENSP00000515586.1:n.1265+4065_1265+4068delinsTGTG
ENST00000703953.1:c.*834-173_*834-170delinsTGTG	ENSP00000515587.1:n.*834-173_*834-170delinsTGTG
ENST00000703954.1:c.1451-173_1451-170delinsTGTG	ENSP00000515588.1:n.1451-173_1451-170delinsTGTG
ENST00000703955.1:n.2121-173_2121-170delinsTGTG
ENST00000703957.1:n.76-173_76-170delinsTGTG
ENST00000298649.8:c.1568-173_1568-170delinsTGTG	ENSP00000298649.3:n.1568-173_1568-170delinsTGTG
ENST00000359426.7:c.1571-173_1571-170delinsTGTG MANE Select	ENSP00000352398.6:n.1571-173_1571-170delinsTGTG
ENST00000436817.6:c.1583-173_1583-170delinsTGTG	ENSP00000415949.2:n.1583-173_1583-170delinsTGTG
ENST00000493591.6:c.*1459-173_*1459-170delinsTGTG	ENSP00000494917.1:n.*1459-173_*1459-170delinsTGTG
ENST00000643399.2:c.1583-173_1583-170delinsTGTG MANE Plus Clinical	ENSP00000494664.1:n.1583-173_1583-170delinsTGTG
ENST00000298649.7:c.1568-173_1568-170delinsTGTG	ENSP00000298649.3:n.1568-173_1568-170delinsTGTG
ENST00000359426.6:c.1571-173_1571-170delinsTGTG	ENSP00000352398.6:n.1571-173_1571-170delinsTGTG
ENST00000360289.6:c.1535-173_1535-170delinsTGTG	ENSP00000353433.2:n.1535-173_1535-170delinsTGTG
ENST00000448642.6:c.1583-173_1583-170delinsTGTG	ENSP00000402103.3:n.1583-173_1583-170delinsTGTG
ENST00000494253.1:n.1797-173_1797-170delinsTGTG
NM_000188.2:c.1571-173_1571-170delinsTGTG	NP_000179.2:n.1571-173_1571-170delinsTGTG
NM_033496.2:c.1568-173_1568-170delinsTGTG	NP_277031.1:n.1568-173_1568-170delinsTGTG
NM_033497.2:c.1583-173_1583-170delinsTGTG	NP_277032.1:n.1583-173_1583-170delinsTGTG
NM_033498.2:c.1583-173_1583-170delinsTGTG	NP_277033.1:n.1583-173_1583-170delinsTGTG
NM_033500.2:c.1535-173_1535-170delinsTGTG , LRG_365t1:c.1535-173_1535-170delinsTGTG	NP_277035.2:n.1535-173_1535-170delinsTGTG
XM_005269735.2:c.1700-173_1700-170delinsTGTG	XP_005269792.1:n.1700-173_1700-170delinsTGTG
XM_005269736.1:c.1583-173_1583-170delinsTGTG	XP_005269793.1:n.1583-173_1583-170delinsTGTG
XM_005269737.1:c.1487-173_1487-170delinsTGTG	XP_005269794.1:n.1487-173_1487-170delinsTGTG
XM_011539732.1:c.1535-173_1535-170delinsTGTG	XP_011538034.1:n.1535-173_1535-170delinsTGTG
XM_011539733.1:c.1529-173_1529-170delinsTGTG	XP_011538035.1:n.1529-173_1529-170delinsTGTG
XM_011539734.1:c.1526-173_1526-170delinsTGTG	XP_011538036.1:n.1526-173_1526-170delinsTGTG
NM_001322364.1:c.1583-173_1583-170delinsTGTG	NP_001309293.1:n.1583-173_1583-170delinsTGTG
NM_001322365.1:c.1676-173_1676-170delinsTGTG	NP_001309294.1:n.1676-173_1676-170delinsTGTG
NM_001322366.1:c.1487-173_1487-170delinsTGTG	NP_001309295.1:n.1487-173_1487-170delinsTGTG
NM_001322367.1:c.1475-173_1475-170delinsTGTG	NP_001309296.1:n.1475-173_1475-170delinsTGTG
NM_001358263.1:c.1583-173_1583-170delinsTGTG MANE Plus Clinical	NP_001345192.1:n.1583-173_1583-170delinsTGTG
XM_024447969.1:c.1583-173_1583-170delinsTGTG	XP_024303737.1:n.1583-173_1583-170delinsTGTG
NM_000188.3:c.1571-173_1571-170delinsTGTG MANE Select	NP_000179.2:n.1571-173_1571-170delinsTGTG
NM_001322364.2:c.1583-173_1583-170delinsTGTG	NP_001309293.1:n.1583-173_1583-170delinsTGTG
NM_001322365.2:c.1676-173_1676-170delinsTGTG	NP_001309294.1:n.1676-173_1676-170delinsTGTG
NM_033496.3:c.1568-173_1568-170delinsTGTG	NP_277031.1:n.1568-173_1568-170delinsTGTG
NM_033497.3:c.1583-173_1583-170delinsTGTG	NP_277032.1:n.1583-173_1583-170delinsTGTG
NM_033498.3:c.1583-173_1583-170delinsTGTG	NP_277033.1:n.1583-173_1583-170delinsTGTG