Canonical Allele Identifier: CA5532571
Gene: HK1 HGNC NCBI

Linked Data

dbSNP Id: rs758179223

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.69382494C>T , CM000672.2:g.69382494C>T GRCh38
NC_000010.10:g.71142250C>T , CM000672.1:g.71142250C>T GRCh37
NC_000010.9:g.70812256C>T NCBI36
NG_012077.1:g.117495C>T , LRG_365:g.117495C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000470050.2:c.1273C>T ENSP00000515580.1:p.Arg425Trp
ENST00000703945.1:c.1189C>T ENSP00000515578.1:p.Arg397Trp
ENST00000703946.1:c.1265+2399C>T ENSP00000515579.1:n.1265+2399C>T
ENST00000703947.1:c.883C>T ENSP00000515581.1:p.Arg295Trp
ENST00000703948.1:c.*890C>T ENSP00000515582.1:n.*890C>T
ENST00000703949.1:c.1273C>T ENSP00000515583.1:p.Arg425Trp
ENST00000703950.1:c.1273C>T ENSP00000515584.1:p.Arg425Trp
ENST00000703951.1:c.1265+2399C>T ENSP00000515585.1:n.1265+2399C>T
ENST00000703952.1:c.1265+2399C>T ENSP00000515586.1:n.1265+2399C>T
ENST00000703953.1:c.*536C>T ENSP00000515587.1:n.*536C>T
ENST00000703954.1:c.1153C>T ENSP00000515588.1:p.Arg385Trp
ENST00000703955.1:n.1823C>T
ENST00000298649.8:c.1270C>T ENSP00000298649.3:p.Arg424Trp
ENST00000359426.7:c.1273C>T MANE Select ENSP00000352398.6:p.Arg425Trp
ENST00000436817.6:c.1285C>T ENSP00000415949.2:p.Arg429Trp
ENST00000493591.6:c.*1161C>T ENSP00000494917.1:n.*1161C>T
ENST00000643399.2:c.1285C>T MANE Plus Clinical ENSP00000494664.1:p.Arg429Trp
ENST00000298649.7:c.1270C>T ENSP00000298649.3:p.Arg424Trp
ENST00000359426.6:c.1273C>T ENSP00000352398.6:p.Arg425Trp
ENST00000360289.6:c.1237C>T ENSP00000353433.2:p.Arg413Trp
ENST00000448642.6:c.1285C>T ENSP00000402103.3:p.Arg429Trp
ENST00000494253.1:n.1499C>T
NM_000188.2:c.1273C>T NP_000179.2:p.Arg425Trp
NM_033496.2:c.1270C>T NP_277031.1:p.Arg424Trp
NM_033497.2:c.1285C>T NP_277032.1:p.Arg429Trp
NM_033498.2:c.1285C>T NP_277033.1:p.Arg429Trp
NM_033500.2:c.1237C>T , LRG_365t1:c.1237C>T NP_277035.2:p.Arg413Trp
XM_005269735.2:c.1402C>T XP_005269792.1:p.Arg468Trp
XM_005269736.1:c.1285C>T XP_005269793.1:p.Arg429Trp
XM_005269737.1:c.1189C>T XP_005269794.1:p.Arg397Trp
XM_011539732.1:c.1237C>T XP_011538034.1:p.Arg413Trp
XM_011539733.1:c.1231C>T XP_011538035.1:p.Arg411Trp
XM_011539734.1:c.1228C>T XP_011538036.1:p.Arg410Trp
NM_001322364.1:c.1285C>T NP_001309293.1:p.Arg429Trp
NM_001322365.1:c.1378C>T NP_001309294.1:p.Arg460Trp
NM_001322366.1:c.1189C>T NP_001309295.1:p.Arg397Trp
NM_001322367.1:c.1177C>T NP_001309296.1:p.Arg393Trp
NM_001358263.1:c.1285C>T MANE Plus Clinical NP_001345192.1:p.Arg429Trp
XM_024447969.1:c.1285C>T XP_024303737.1:p.Arg429Trp
NM_000188.3:c.1273C>T MANE Select NP_000179.2:p.Arg425Trp
NM_001322364.2:c.1285C>T NP_001309293.1:p.Arg429Trp
NM_001322365.2:c.1378C>T NP_001309294.1:p.Arg460Trp
NM_033496.3:c.1270C>T NP_277031.1:p.Arg424Trp
NM_033497.3:c.1285C>T NP_277032.1:p.Arg429Trp
NM_033498.3:c.1285C>T NP_277033.1:p.Arg429Trp