Canonical Allele Identifier: CA376909734
Gene: HK1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.69382600C>A , CM000672.2:g.69382600C>A GRCh38
NC_000010.10:g.71142356C>A , CM000672.1:g.71142356C>A GRCh37
NC_000010.9:g.70812362C>A NCBI36
NG_012077.1:g.117601C>A , LRG_365:g.117601C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000470050.2:c.1379C>A ENSP00000515580.1:p.Ala460Asp
ENST00000703945.1:c.1295C>A ENSP00000515578.1:p.Ala432Asp
ENST00000703946.1:c.1265+2505C>A ENSP00000515579.1:n.1265+2505C>A
ENST00000703947.1:c.989C>A ENSP00000515581.1:p.Ala330Asp
ENST00000703948.1:c.*996C>A ENSP00000515582.1:n.*996C>A
ENST00000703949.1:c.1379C>A ENSP00000515583.1:p.Ala460Asp
ENST00000703950.1:c.1379C>A ENSP00000515584.1:p.Ala460Asp
ENST00000703951.1:c.1265+2505C>A ENSP00000515585.1:n.1265+2505C>A
ENST00000703952.1:c.1265+2505C>A ENSP00000515586.1:n.1265+2505C>A
ENST00000703953.1:c.*642C>A ENSP00000515587.1:n.*642C>A
ENST00000703954.1:c.1259C>A ENSP00000515588.1:p.Ala420Asp
ENST00000703955.1:n.1929C>A
ENST00000298649.8:c.1376C>A ENSP00000298649.3:p.Ala459Asp
ENST00000359426.7:c.1379C>A MANE Select ENSP00000352398.6:p.Ala460Asp
ENST00000436817.6:c.1391C>A ENSP00000415949.2:p.Ala464Asp
ENST00000493591.6:c.*1267C>A ENSP00000494917.1:n.*1267C>A
ENST00000643399.2:c.1391C>A MANE Plus Clinical ENSP00000494664.1:p.Ala464Asp
ENST00000298649.7:c.1376C>A ENSP00000298649.3:p.Ala459Asp
ENST00000359426.6:c.1379C>A ENSP00000352398.6:p.Ala460Asp
ENST00000360289.6:c.1343C>A ENSP00000353433.2:p.Ala448Asp
ENST00000448642.6:c.1391C>A ENSP00000402103.3:p.Ala464Asp
ENST00000494253.1:n.1605C>A
NM_000188.2:c.1379C>A NP_000179.2:p.Ala460Asp
NM_033496.2:c.1376C>A NP_277031.1:p.Ala459Asp
NM_033497.2:c.1391C>A NP_277032.1:p.Ala464Asp
NM_033498.2:c.1391C>A NP_277033.1:p.Ala464Asp
NM_033500.2:c.1343C>A , LRG_365t1:c.1343C>A NP_277035.2:p.Ala448Asp
XM_005269735.2:c.1508C>A XP_005269792.1:p.Ala503Asp
XM_005269736.1:c.1391C>A XP_005269793.1:p.Ala464Asp
XM_005269737.1:c.1295C>A XP_005269794.1:p.Ala432Asp
XM_011539732.1:c.1343C>A XP_011538034.1:p.Ala448Asp
XM_011539733.1:c.1337C>A XP_011538035.1:p.Ala446Asp
XM_011539734.1:c.1334C>A XP_011538036.1:p.Ala445Asp
NM_001322364.1:c.1391C>A NP_001309293.1:p.Ala464Asp
NM_001322365.1:c.1484C>A NP_001309294.1:p.Ala495Asp
NM_001322366.1:c.1295C>A NP_001309295.1:p.Ala432Asp
NM_001322367.1:c.1283C>A NP_001309296.1:p.Ala428Asp
NM_001358263.1:c.1391C>A MANE Plus Clinical NP_001345192.1:p.Ala464Asp
XM_024447969.1:c.1391C>A XP_024303737.1:p.Ala464Asp
NM_000188.3:c.1379C>A MANE Select NP_000179.2:p.Ala460Asp
NM_001322364.2:c.1391C>A NP_001309293.1:p.Ala464Asp
NM_001322365.2:c.1484C>A NP_001309294.1:p.Ala495Asp
NM_033496.3:c.1376C>A NP_277031.1:p.Ala459Asp
NM_033497.3:c.1391C>A NP_277032.1:p.Ala464Asp
NM_033498.3:c.1391C>A NP_277033.1:p.Ala464Asp