Canonical Allele Identifier: CA2609447221
Gene: HK1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.69384298_69384299dup , CM000672.2:g.69384298_69384299dup GRCh38
NC_000010.10:g.71144054_71144055dup , CM000672.1:g.71144054_71144055dup GRCh37
NC_000010.9:g.70814060_70814061dup NCBI36
NG_012077.1:g.119299_119300dup , LRG_365:g.119299_119300dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000470050.2:c.1571-35_1571-34dup ENSP00000515580.1:n.1571-35_1571-34dup
ENST00000703945.1:c.1487-35_1487-34dup ENSP00000515578.1:n.1487-35_1487-34dup
ENST00000703946.1:c.1265+4203_1265+4204dup ENSP00000515579.1:n.1265+4203_1265+4204dup
ENST00000703947.1:c.1181-35_1181-34dup ENSP00000515581.1:n.1181-35_1181-34dup
ENST00000703948.1:c.*1188-35_*1188-34dup ENSP00000515582.1:n.*1188-35_*1188-34dup
ENST00000703949.1:c.1571-35_1571-34dup ENSP00000515583.1:n.1571-35_1571-34dup
ENST00000703950.1:c.1571-35_1571-34dup ENSP00000515584.1:n.1571-35_1571-34dup
ENST00000703951.1:c.1265+4203_1265+4204dup ENSP00000515585.1:n.1265+4203_1265+4204dup
ENST00000703952.1:c.1265+4203_1265+4204dup ENSP00000515586.1:n.1265+4203_1265+4204dup
ENST00000703953.1:c.*834-35_*834-34dup ENSP00000515587.1:n.*834-35_*834-34dup
ENST00000703954.1:c.1451-35_1451-34dup ENSP00000515588.1:n.1451-35_1451-34dup
ENST00000703955.1:n.2121-35_2121-34dup
ENST00000703957.1:n.76-35_76-34dup
ENST00000298649.8:c.1568-35_1568-34dup ENSP00000298649.3:n.1568-35_1568-34dup
ENST00000359426.7:c.1571-35_1571-34dup MANE Select ENSP00000352398.6:n.1571-35_1571-34dup
ENST00000436817.6:c.1583-35_1583-34dup ENSP00000415949.2:n.1583-35_1583-34dup
ENST00000493591.6:c.*1459-35_*1459-34dup ENSP00000494917.1:n.*1459-35_*1459-34dup
ENST00000643399.2:c.1583-35_1583-34dup MANE Plus Clinical ENSP00000494664.1:n.1583-35_1583-34dup
ENST00000298649.7:c.1568-35_1568-34dup ENSP00000298649.3:n.1568-35_1568-34dup
ENST00000359426.6:c.1571-35_1571-34dup ENSP00000352398.6:n.1571-35_1571-34dup
ENST00000360289.6:c.1535-35_1535-34dup ENSP00000353433.2:n.1535-35_1535-34dup
ENST00000448642.6:c.1583-35_1583-34dup ENSP00000402103.3:n.1583-35_1583-34dup
ENST00000494253.1:n.1797-35_1797-34dup
NM_000188.2:c.1571-35_1571-34dup NP_000179.2:n.1571-35_1571-34dup
NM_033496.2:c.1568-35_1568-34dup NP_277031.1:n.1568-35_1568-34dup
NM_033497.2:c.1583-35_1583-34dup NP_277032.1:n.1583-35_1583-34dup
NM_033498.2:c.1583-35_1583-34dup NP_277033.1:n.1583-35_1583-34dup
NM_033500.2:c.1535-35_1535-34dup , LRG_365t1:c.1535-35_1535-34dup NP_277035.2:n.1535-35_1535-34dup
XM_005269735.2:c.1700-35_1700-34dup XP_005269792.1:n.1700-35_1700-34dup
XM_005269736.1:c.1583-35_1583-34dup XP_005269793.1:n.1583-35_1583-34dup
XM_005269737.1:c.1487-35_1487-34dup XP_005269794.1:n.1487-35_1487-34dup
XM_011539732.1:c.1535-35_1535-34dup XP_011538034.1:n.1535-35_1535-34dup
XM_011539733.1:c.1529-35_1529-34dup XP_011538035.1:n.1529-35_1529-34dup
XM_011539734.1:c.1526-35_1526-34dup XP_011538036.1:n.1526-35_1526-34dup
NM_001322364.1:c.1583-35_1583-34dup NP_001309293.1:n.1583-35_1583-34dup
NM_001322365.1:c.1676-35_1676-34dup NP_001309294.1:n.1676-35_1676-34dup
NM_001322366.1:c.1487-35_1487-34dup NP_001309295.1:n.1487-35_1487-34dup
NM_001322367.1:c.1475-35_1475-34dup NP_001309296.1:n.1475-35_1475-34dup
NM_001358263.1:c.1583-35_1583-34dup MANE Plus Clinical NP_001345192.1:n.1583-35_1583-34dup
XM_024447969.1:c.1583-35_1583-34dup XP_024303737.1:n.1583-35_1583-34dup
NM_000188.3:c.1571-35_1571-34dup MANE Select NP_000179.2:n.1571-35_1571-34dup
NM_001322364.2:c.1583-35_1583-34dup NP_001309293.1:n.1583-35_1583-34dup
NM_001322365.2:c.1676-35_1676-34dup NP_001309294.1:n.1676-35_1676-34dup
NM_033496.3:c.1568-35_1568-34dup NP_277031.1:n.1568-35_1568-34dup
NM_033497.3:c.1583-35_1583-34dup NP_277032.1:n.1583-35_1583-34dup
NM_033498.3:c.1583-35_1583-34dup NP_277033.1:n.1583-35_1583-34dup