Canonical Allele Identifier: CA470276495

Gene: HK1

Linked Data

• MyVariant Identifiers: chr10:g.71142348G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69382592G>C , CM000672.2:g.69382592G>C	GRCh38
NC_000010.10:g.71142348G>C , CM000672.1:g.71142348G>C	GRCh37
NC_000010.9:g.70812354G>C	NCBI36
NG_012077.1:g.117593G>C , LRG_365:g.117593G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000470050.2:c.1371G>C	ENSP00000515580.1:p.Thr457=
ENST00000703945.1:c.1287G>C	ENSP00000515578.1:p.Thr429=
ENST00000703946.1:c.1265+2497G>C	ENSP00000515579.1:n.1265+2497G>C
ENST00000703947.1:c.981G>C	ENSP00000515581.1:p.Thr327=
ENST00000703948.1:c.*988G>C	ENSP00000515582.1:n.*988G>C
ENST00000703949.1:c.1371G>C	ENSP00000515583.1:p.Thr457=
ENST00000703950.1:c.1371G>C	ENSP00000515584.1:p.Thr457=
ENST00000703951.1:c.1265+2497G>C	ENSP00000515585.1:n.1265+2497G>C
ENST00000703952.1:c.1265+2497G>C	ENSP00000515586.1:n.1265+2497G>C
ENST00000703953.1:c.*634G>C	ENSP00000515587.1:n.*634G>C
ENST00000703954.1:c.1251G>C	ENSP00000515588.1:p.Thr417=
ENST00000703955.1:n.1921G>C
ENST00000298649.8:c.1368G>C	ENSP00000298649.3:p.Thr456=
ENST00000359426.7:c.1371G>C MANE Select	ENSP00000352398.6:p.Thr457=
ENST00000436817.6:c.1383G>C	ENSP00000415949.2:p.Thr461=
ENST00000493591.6:c.*1259G>C	ENSP00000494917.1:n.*1259G>C
ENST00000643399.2:c.1383G>C MANE Plus Clinical	ENSP00000494664.1:p.Thr461=
ENST00000298649.7:c.1368G>C	ENSP00000298649.3:p.Thr456=
ENST00000359426.6:c.1371G>C	ENSP00000352398.6:p.Thr457=
ENST00000360289.6:c.1335G>C	ENSP00000353433.2:p.Thr445=
ENST00000448642.6:c.1383G>C	ENSP00000402103.3:p.Thr461=
ENST00000494253.1:n.1597G>C
NM_000188.2:c.1371G>C	NP_000179.2:p.Thr457=
NM_033496.2:c.1368G>C	NP_277031.1:p.Thr456=
NM_033497.2:c.1383G>C	NP_277032.1:p.Thr461=
NM_033498.2:c.1383G>C	NP_277033.1:p.Thr461=
NM_033500.2:c.1335G>C , LRG_365t1:c.1335G>C	NP_277035.2:p.Thr445=
XM_005269735.2:c.1500G>C	XP_005269792.1:p.Thr500=
XM_005269736.1:c.1383G>C	XP_005269793.1:p.Thr461=
XM_005269737.1:c.1287G>C	XP_005269794.1:p.Thr429=
XM_011539732.1:c.1335G>C	XP_011538034.1:p.Thr445=
XM_011539733.1:c.1329G>C	XP_011538035.1:p.Thr443=
XM_011539734.1:c.1326G>C	XP_011538036.1:p.Thr442=
NM_001322364.1:c.1383G>C	NP_001309293.1:p.Thr461=
NM_001322365.1:c.1476G>C	NP_001309294.1:p.Thr492=
NM_001322366.1:c.1287G>C	NP_001309295.1:p.Thr429=
NM_001322367.1:c.1275G>C	NP_001309296.1:p.Thr425=
NM_001358263.1:c.1383G>C MANE Plus Clinical	NP_001345192.1:p.Thr461=
XM_024447969.1:c.1383G>C	XP_024303737.1:p.Thr461=
NM_000188.3:c.1371G>C MANE Select	NP_000179.2:p.Thr457=
NM_001322364.2:c.1383G>C	NP_001309293.1:p.Thr461=
NM_001322365.2:c.1476G>C	NP_001309294.1:p.Thr492=
NM_033496.3:c.1368G>C	NP_277031.1:p.Thr456=
NM_033497.3:c.1383G>C	NP_277032.1:p.Thr461=
NM_033498.3:c.1383G>C	NP_277033.1:p.Thr461=