Canonical Allele Identifier: CA376910895
Gene: HK1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.69384342A>T , CM000672.2:g.69384342A>T GRCh38
NC_000010.10:g.71144098A>T , CM000672.1:g.71144098A>T GRCh37
NC_000010.9:g.70814104A>T NCBI36
NG_012077.1:g.119343A>T , LRG_365:g.119343A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000470050.2:c.1580A>T ENSP00000515580.1:p.Asp527Val
ENST00000703945.1:c.1496A>T ENSP00000515578.1:p.Asp499Val
ENST00000703946.1:c.1265+4247A>T ENSP00000515579.1:n.1265+4247A>T
ENST00000703947.1:c.1190A>T ENSP00000515581.1:p.Asp397Val
ENST00000703948.1:c.*1197A>T ENSP00000515582.1:n.*1197A>T
ENST00000703949.1:c.1580A>T ENSP00000515583.1:p.Asp527Val
ENST00000703950.1:c.1580A>T ENSP00000515584.1:p.Asp527Val
ENST00000703951.1:c.1265+4247A>T ENSP00000515585.1:n.1265+4247A>T
ENST00000703952.1:c.1265+4247A>T ENSP00000515586.1:n.1265+4247A>T
ENST00000703953.1:c.*843A>T ENSP00000515587.1:n.*843A>T
ENST00000703954.1:c.1460A>T ENSP00000515588.1:p.Asp487Val
ENST00000703955.1:n.2130A>T
ENST00000703957.1:n.85A>T
ENST00000298649.8:c.1577A>T ENSP00000298649.3:p.Asp526Val
ENST00000359426.7:c.1580A>T MANE Select ENSP00000352398.6:p.Asp527Val
ENST00000436817.6:c.1592A>T ENSP00000415949.2:p.Asp531Val
ENST00000493591.6:c.*1468A>T ENSP00000494917.1:n.*1468A>T
ENST00000643399.2:c.1592A>T MANE Plus Clinical ENSP00000494664.1:p.Asp531Val
ENST00000298649.7:c.1577A>T ENSP00000298649.3:p.Asp526Val
ENST00000359426.6:c.1580A>T ENSP00000352398.6:p.Asp527Val
ENST00000360289.6:c.1544A>T ENSP00000353433.2:p.Asp515Val
ENST00000448642.6:c.1592A>T ENSP00000402103.3:p.Asp531Val
ENST00000494253.1:n.1806A>T
NM_000188.2:c.1580A>T NP_000179.2:p.Asp527Val
NM_033496.2:c.1577A>T NP_277031.1:p.Asp526Val
NM_033497.2:c.1592A>T NP_277032.1:p.Asp531Val
NM_033498.2:c.1592A>T NP_277033.1:p.Asp531Val
NM_033500.2:c.1544A>T , LRG_365t1:c.1544A>T NP_277035.2:p.Asp515Val
XM_005269735.2:c.1709A>T XP_005269792.1:p.Asp570Val
XM_005269736.1:c.1592A>T XP_005269793.1:p.Asp531Val
XM_005269737.1:c.1496A>T XP_005269794.1:p.Asp499Val
XM_011539732.1:c.1544A>T XP_011538034.1:p.Asp515Val
XM_011539733.1:c.1538A>T XP_011538035.1:p.Asp513Val
XM_011539734.1:c.1535A>T XP_011538036.1:p.Asp512Val
NM_001322364.1:c.1592A>T NP_001309293.1:p.Asp531Val
NM_001322365.1:c.1685A>T NP_001309294.1:p.Asp562Val
NM_001322366.1:c.1496A>T NP_001309295.1:p.Asp499Val
NM_001322367.1:c.1484A>T NP_001309296.1:p.Asp495Val
NM_001358263.1:c.1592A>T MANE Plus Clinical NP_001345192.1:p.Asp531Val
XM_024447969.1:c.1592A>T XP_024303737.1:p.Asp531Val
NM_000188.3:c.1580A>T MANE Select NP_000179.2:p.Asp527Val
NM_001322364.2:c.1592A>T NP_001309293.1:p.Asp531Val
NM_001322365.2:c.1685A>T NP_001309294.1:p.Asp562Val
NM_033496.3:c.1577A>T NP_277031.1:p.Asp526Val
NM_033497.3:c.1592A>T NP_277032.1:p.Asp531Val
NM_033498.3:c.1592A>T NP_277033.1:p.Asp531Val