Canonical Allele Identifier: CA376917441

Gene: HK1

Linked Data

• MyVariant Identifiers: chr10:g.71139730T>G (hg19) ; chr10:g.69379974T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69379974T>G , CM000672.2:g.69379974T>G	GRCh38
NC_000010.10:g.71139730T>G , CM000672.1:g.71139730T>G	GRCh37
NC_000010.9:g.70809736T>G	NCBI36
NG_012077.1:g.114975T>G , LRG_365:g.114975T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000470050.2:c.1144T>G	ENSP00000515580.1:p.Ser382Ala
ENST00000703945.1:c.1060T>G	ENSP00000515578.1:p.Ser354Ala
ENST00000703946.1:c.1144T>G	ENSP00000515579.1:p.Ser382Ala
ENST00000703947.1:c.876-2513T>G	ENSP00000515581.1:n.876-2513T>G
ENST00000703948.1:c.*761T>G	ENSP00000515582.1:n.*761T>G
ENST00000703949.1:c.1144T>G	ENSP00000515583.1:p.Ser382Ala
ENST00000703950.1:c.1144T>G	ENSP00000515584.1:p.Ser382Ala
ENST00000703951.1:c.1144T>G	ENSP00000515585.1:p.Ser382Ala
ENST00000703952.1:c.1144T>G	ENSP00000515586.1:p.Ser382Ala
ENST00000703953.1:c.*407T>G	ENSP00000515587.1:n.*407T>G
ENST00000703954.1:c.1024T>G	ENSP00000515588.1:p.Ser342Ala
ENST00000703955.1:n.1694T>G
ENST00000298649.8:c.1141T>G	ENSP00000298649.3:p.Ser381Ala
ENST00000359426.7:c.1144T>G MANE Select	ENSP00000352398.6:p.Ser382Ala
ENST00000436817.6:c.1156T>G	ENSP00000415949.2:p.Ser386Ala
ENST00000493591.6:c.*1032T>G	ENSP00000494917.1:n.*1032T>G
ENST00000643399.2:c.1156T>G MANE Plus Clinical	ENSP00000494664.1:p.Ser386Ala
ENST00000298649.7:c.1141T>G	ENSP00000298649.3:p.Ser381Ala
ENST00000359426.6:c.1144T>G	ENSP00000352398.6:p.Ser382Ala
ENST00000360289.6:c.1108T>G	ENSP00000353433.2:p.Ser370Ala
ENST00000448642.6:c.1156T>G	ENSP00000402103.3:p.Ser386Ala
ENST00000494253.1:n.1370T>G
NM_000188.2:c.1144T>G	NP_000179.2:p.Ser382Ala
NM_033496.2:c.1141T>G	NP_277031.1:p.Ser381Ala
NM_033497.2:c.1156T>G	NP_277032.1:p.Ser386Ala
NM_033498.2:c.1156T>G	NP_277033.1:p.Ser386Ala
NM_033500.2:c.1108T>G , LRG_365t1:c.1108T>G	NP_277035.2:p.Ser370Ala
XM_005269735.2:c.1273T>G	XP_005269792.1:p.Ser425Ala
XM_005269736.1:c.1156T>G	XP_005269793.1:p.Ser386Ala
XM_005269737.1:c.1060T>G	XP_005269794.1:p.Ser354Ala
XM_011539732.1:c.1108T>G	XP_011538034.1:p.Ser370Ala
XM_011539733.1:c.1102T>G	XP_011538035.1:p.Ser368Ala
XM_011539734.1:c.1099T>G	XP_011538036.1:p.Ser367Ala
NM_001322364.1:c.1156T>G	NP_001309293.1:p.Ser386Ala
NM_001322365.1:c.1249T>G	NP_001309294.1:p.Ser417Ala
NM_001322366.1:c.1060T>G	NP_001309295.1:p.Ser354Ala
NM_001322367.1:c.1048T>G	NP_001309296.1:p.Ser350Ala
NM_001358263.1:c.1156T>G MANE Plus Clinical	NP_001345192.1:p.Ser386Ala
XM_024447969.1:c.1156T>G	XP_024303737.1:p.Ser386Ala
NM_000188.3:c.1144T>G MANE Select	NP_000179.2:p.Ser382Ala
NM_001322364.2:c.1156T>G	NP_001309293.1:p.Ser386Ala
NM_001322365.2:c.1249T>G	NP_001309294.1:p.Ser417Ala
NM_033496.3:c.1141T>G	NP_277031.1:p.Ser381Ala
NM_033497.3:c.1156T>G	NP_277032.1:p.Ser386Ala
NM_033498.3:c.1156T>G	NP_277033.1:p.Ser386Ala