Canonical Allele Identifier: CA376909730
Gene: HK1 HGNC NCBI

Linked Data

dbSNP Id: rs1589570939

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.69382597T>G , CM000672.2:g.69382597T>G GRCh38
NC_000010.10:g.71142353T>G , CM000672.1:g.71142353T>G GRCh37
NC_000010.9:g.70812359T>G NCBI36
NG_012077.1:g.117598T>G , LRG_365:g.117598T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000470050.2:c.1376T>G ENSP00000515580.1:p.Val459Gly
ENST00000703945.1:c.1292T>G ENSP00000515578.1:p.Val431Gly
ENST00000703946.1:c.1265+2502T>G ENSP00000515579.1:n.1265+2502T>G
ENST00000703947.1:c.986T>G ENSP00000515581.1:p.Val329Gly
ENST00000703948.1:c.*993T>G ENSP00000515582.1:n.*993T>G
ENST00000703949.1:c.1376T>G ENSP00000515583.1:p.Val459Gly
ENST00000703950.1:c.1376T>G ENSP00000515584.1:p.Val459Gly
ENST00000703951.1:c.1265+2502T>G ENSP00000515585.1:n.1265+2502T>G
ENST00000703952.1:c.1265+2502T>G ENSP00000515586.1:n.1265+2502T>G
ENST00000703953.1:c.*639T>G ENSP00000515587.1:n.*639T>G
ENST00000703954.1:c.1256T>G ENSP00000515588.1:p.Val419Gly
ENST00000703955.1:n.1926T>G
ENST00000298649.8:c.1373T>G ENSP00000298649.3:p.Val458Gly
ENST00000359426.7:c.1376T>G MANE Select ENSP00000352398.6:p.Val459Gly
ENST00000436817.6:c.1388T>G ENSP00000415949.2:p.Val463Gly
ENST00000493591.6:c.*1264T>G ENSP00000494917.1:n.*1264T>G
ENST00000643399.2:c.1388T>G MANE Plus Clinical ENSP00000494664.1:p.Val463Gly
ENST00000298649.7:c.1373T>G ENSP00000298649.3:p.Val458Gly
ENST00000359426.6:c.1376T>G ENSP00000352398.6:p.Val459Gly
ENST00000360289.6:c.1340T>G ENSP00000353433.2:p.Val447Gly
ENST00000448642.6:c.1388T>G ENSP00000402103.3:p.Val463Gly
ENST00000494253.1:n.1602T>G
NM_000188.2:c.1376T>G NP_000179.2:p.Val459Gly
NM_033496.2:c.1373T>G NP_277031.1:p.Val458Gly
NM_033497.2:c.1388T>G NP_277032.1:p.Val463Gly
NM_033498.2:c.1388T>G NP_277033.1:p.Val463Gly
NM_033500.2:c.1340T>G , LRG_365t1:c.1340T>G NP_277035.2:p.Val447Gly
XM_005269735.2:c.1505T>G XP_005269792.1:p.Val502Gly
XM_005269736.1:c.1388T>G XP_005269793.1:p.Val463Gly
XM_005269737.1:c.1292T>G XP_005269794.1:p.Val431Gly
XM_011539732.1:c.1340T>G XP_011538034.1:p.Val447Gly
XM_011539733.1:c.1334T>G XP_011538035.1:p.Val445Gly
XM_011539734.1:c.1331T>G XP_011538036.1:p.Val444Gly
NM_001322364.1:c.1388T>G NP_001309293.1:p.Val463Gly
NM_001322365.1:c.1481T>G NP_001309294.1:p.Val494Gly
NM_001322366.1:c.1292T>G NP_001309295.1:p.Val431Gly
NM_001322367.1:c.1280T>G NP_001309296.1:p.Val427Gly
NM_001358263.1:c.1388T>G MANE Plus Clinical NP_001345192.1:p.Val463Gly
XM_024447969.1:c.1388T>G XP_024303737.1:p.Val463Gly
NM_000188.3:c.1376T>G MANE Select NP_000179.2:p.Val459Gly
NM_001322364.2:c.1388T>G NP_001309293.1:p.Val463Gly
NM_001322365.2:c.1481T>G NP_001309294.1:p.Val494Gly
NM_033496.3:c.1373T>G NP_277031.1:p.Val458Gly
NM_033497.3:c.1388T>G NP_277032.1:p.Val463Gly
NM_033498.3:c.1388T>G NP_277033.1:p.Val463Gly