Canonical Allele Identifier: CA2609447241

Gene: HK1

Linked Data

• gnomAD v4: 10-69384512-C-CTATGGTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69384513_69384514insATGGTTTT , CM000672.2:g.69384513_69384514insATGGTTTT	GRCh38
NC_000010.10:g.71144269_71144270insATGGTTTT , CM000672.1:g.71144269_71144270insATGGTTTT	GRCh37
NC_000010.9:g.70814275_70814276insATGGTTTT	NCBI36
NG_012077.1:g.119514_119515insATGGTTTT , LRG_365:g.119514_119515insATGGTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470050.2:c.1719+32_1719+33insATGGTTTT	ENSP00000515580.1:n.1719+32_1719+33insATGGTTTT
ENST00000703945.1:c.1635+32_1635+33insATGGTTTT	ENSP00000515578.1:n.1635+32_1635+33insATGGTTTT
ENST00000703946.1:c.1265+4418_1265+4419insATGGTTTT	ENSP00000515579.1:n.1265+4418_1265+4419insATGGTTTT
ENST00000703947.1:c.1329+32_1329+33insATGGTTTT	ENSP00000515581.1:n.1329+32_1329+33insATGGTTTT
ENST00000703948.1:c.*1336+32_*1336+33insATGGTTTT	ENSP00000515582.1:n.*1336+32_*1336+33insATGGTTTT
ENST00000703949.1:c.1719+32_1719+33insATGGTTTT	ENSP00000515583.1:n.1719+32_1719+33insATGGTTTT
ENST00000703950.1:c.1719+32_1719+33insATGGTTTT	ENSP00000515584.1:n.1719+32_1719+33insATGGTTTT
ENST00000703951.1:c.1265+4418_1265+4419insATGGTTTT	ENSP00000515585.1:n.1265+4418_1265+4419insATGGTTTT
ENST00000703952.1:c.1265+4418_1265+4419insATGGTTTT	ENSP00000515586.1:n.1265+4418_1265+4419insATGGTTTT
ENST00000703953.1:c.*982+32_*982+33insATGGTTTT	ENSP00000515587.1:n.*982+32_*982+33insATGGTTTT
ENST00000703954.1:c.1599+32_1599+33insATGGTTTT	ENSP00000515588.1:n.1599+32_1599+33insATGGTTTT
ENST00000703955.1:n.2269+32_2269+33insATGGTTTT
ENST00000703957.1:n.224+32_224+33insATGGTTTT
ENST00000298649.8:c.1716+32_1716+33insATGGTTTT	ENSP00000298649.3:n.1716+32_1716+33insATGGTTTT
ENST00000359426.7:c.1719+32_1719+33insATGGTTTT MANE Select	ENSP00000352398.6:n.1719+32_1719+33insATGGTTTT
ENST00000436817.6:c.1731+32_1731+33insATGGTTTT	ENSP00000415949.2:n.1731+32_1731+33insATGGTTTT
ENST00000493591.6:c.*1607+32_*1607+33insATGGTTTT	ENSP00000494917.1:n.*1607+32_*1607+33insATGGTTTT
ENST00000643399.2:c.1731+32_1731+33insATGGTTTT MANE Plus Clinical	ENSP00000494664.1:n.1731+32_1731+33insATGGTTTT
ENST00000298649.7:c.1716+32_1716+33insATGGTTTT	ENSP00000298649.3:n.1716+32_1716+33insATGGTTTT
ENST00000359426.6:c.1719+32_1719+33insATGGTTTT	ENSP00000352398.6:n.1719+32_1719+33insATGGTTTT
ENST00000360289.6:c.1683+32_1683+33insATGGTTTT	ENSP00000353433.2:n.1683+32_1683+33insATGGTTTT
ENST00000448642.6:c.1731+32_1731+33insATGGTTTT	ENSP00000402103.3:n.1731+32_1731+33insATGGTTTT
ENST00000494253.1:n.1977_1978insATGGTTTT
NM_000188.2:c.1719+32_1719+33insATGGTTTT	NP_000179.2:n.1719+32_1719+33insATGGTTTT
NM_033496.2:c.1716+32_1716+33insATGGTTTT	NP_277031.1:n.1716+32_1716+33insATGGTTTT
NM_033497.2:c.1731+32_1731+33insATGGTTTT	NP_277032.1:n.1731+32_1731+33insATGGTTTT
NM_033498.2:c.1731+32_1731+33insATGGTTTT	NP_277033.1:n.1731+32_1731+33insATGGTTTT
NM_033500.2:c.1683+32_1683+33insATGGTTTT , LRG_365t1:c.1683+32_1683+33insATGGTTTT	NP_277035.2:n.1683+32_1683+33insATGGTTTT
XM_005269735.2:c.1848+32_1848+33insATGGTTTT	XP_005269792.1:n.1848+32_1848+33insATGGTTTT
XM_005269736.1:c.1731+32_1731+33insATGGTTTT	XP_005269793.1:n.1731+32_1731+33insATGGTTTT
XM_005269737.1:c.1635+32_1635+33insATGGTTTT	XP_005269794.1:n.1635+32_1635+33insATGGTTTT
XM_011539732.1:c.1683+32_1683+33insATGGTTTT	XP_011538034.1:n.1683+32_1683+33insATGGTTTT
XM_011539733.1:c.1677+32_1677+33insATGGTTTT	XP_011538035.1:n.1677+32_1677+33insATGGTTTT
XM_011539734.1:c.1674+32_1674+33insATGGTTTT	XP_011538036.1:n.1674+32_1674+33insATGGTTTT
NM_001322364.1:c.1731+32_1731+33insATGGTTTT	NP_001309293.1:n.1731+32_1731+33insATGGTTTT
NM_001322365.1:c.1824+32_1824+33insATGGTTTT	NP_001309294.1:n.1824+32_1824+33insATGGTTTT
NM_001322366.1:c.1635+32_1635+33insATGGTTTT	NP_001309295.1:n.1635+32_1635+33insATGGTTTT
NM_001322367.1:c.1623+32_1623+33insATGGTTTT	NP_001309296.1:n.1623+32_1623+33insATGGTTTT
NM_001358263.1:c.1731+32_1731+33insATGGTTTT MANE Plus Clinical	NP_001345192.1:n.1731+32_1731+33insATGGTTTT
XM_024447969.1:c.1731+32_1731+33insATGGTTTT	XP_024303737.1:n.1731+32_1731+33insATGGTTTT
NM_000188.3:c.1719+32_1719+33insATGGTTTT MANE Select	NP_000179.2:n.1719+32_1719+33insATGGTTTT
NM_001322364.2:c.1731+32_1731+33insATGGTTTT	NP_001309293.1:n.1731+32_1731+33insATGGTTTT
NM_001322365.2:c.1824+32_1824+33insATGGTTTT	NP_001309294.1:n.1824+32_1824+33insATGGTTTT
NM_033496.3:c.1716+32_1716+33insATGGTTTT	NP_277031.1:n.1716+32_1716+33insATGGTTTT
NM_033497.3:c.1731+32_1731+33insATGGTTTT	NP_277032.1:n.1731+32_1731+33insATGGTTTT
NM_033498.3:c.1731+32_1731+33insATGGTTTT	NP_277033.1:n.1731+32_1731+33insATGGTTTT