Canonical Allele Identifier: CA470276534

Gene: HK1

Linked Data

• MyVariant Identifiers: chr10:g.71142364T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69382608T>C , CM000672.2:g.69382608T>C	GRCh38
NC_000010.10:g.71142364T>C , CM000672.1:g.71142364T>C	GRCh37
NC_000010.9:g.70812370T>C	NCBI36
NG_012077.1:g.117609T>C , LRG_365:g.117609T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470050.2:c.1387T>C	ENSP00000515580.1:p.Leu463=
ENST00000703945.1:c.1303T>C	ENSP00000515578.1:p.Leu435=
ENST00000703946.1:c.1265+2513T>C	ENSP00000515579.1:n.1265+2513T>C
ENST00000703947.1:c.997T>C	ENSP00000515581.1:p.Leu333=
ENST00000703948.1:c.*1004T>C	ENSP00000515582.1:n.*1004T>C
ENST00000703949.1:c.1387T>C	ENSP00000515583.1:p.Leu463=
ENST00000703950.1:c.1387T>C	ENSP00000515584.1:p.Leu463=
ENST00000703951.1:c.1265+2513T>C	ENSP00000515585.1:n.1265+2513T>C
ENST00000703952.1:c.1265+2513T>C	ENSP00000515586.1:n.1265+2513T>C
ENST00000703953.1:c.*650T>C	ENSP00000515587.1:n.*650T>C
ENST00000703954.1:c.1267T>C	ENSP00000515588.1:p.Leu423=
ENST00000703955.1:n.1937T>C
ENST00000298649.8:c.1384T>C	ENSP00000298649.3:p.Leu462=
ENST00000359426.7:c.1387T>C MANE Select	ENSP00000352398.6:p.Leu463=
ENST00000436817.6:c.1399T>C	ENSP00000415949.2:p.Leu467=
ENST00000493591.6:c.*1275T>C	ENSP00000494917.1:n.*1275T>C
ENST00000643399.2:c.1399T>C MANE Plus Clinical	ENSP00000494664.1:p.Leu467=
ENST00000298649.7:c.1384T>C	ENSP00000298649.3:p.Leu462=
ENST00000359426.6:c.1387T>C	ENSP00000352398.6:p.Leu463=
ENST00000360289.6:c.1351T>C	ENSP00000353433.2:p.Leu451=
ENST00000448642.6:c.1399T>C	ENSP00000402103.3:p.Leu467=
ENST00000494253.1:n.1613T>C
NM_000188.2:c.1387T>C	NP_000179.2:p.Leu463=
NM_033496.2:c.1384T>C	NP_277031.1:p.Leu462=
NM_033497.2:c.1399T>C	NP_277032.1:p.Leu467=
NM_033498.2:c.1399T>C	NP_277033.1:p.Leu467=
NM_033500.2:c.1351T>C , LRG_365t1:c.1351T>C	NP_277035.2:p.Leu451=
XM_005269735.2:c.1516T>C	XP_005269792.1:p.Leu506=
XM_005269736.1:c.1399T>C	XP_005269793.1:p.Leu467=
XM_005269737.1:c.1303T>C	XP_005269794.1:p.Leu435=
XM_011539732.1:c.1351T>C	XP_011538034.1:p.Leu451=
XM_011539733.1:c.1345T>C	XP_011538035.1:p.Leu449=
XM_011539734.1:c.1342T>C	XP_011538036.1:p.Leu448=
NM_001322364.1:c.1399T>C	NP_001309293.1:p.Leu467=
NM_001322365.1:c.1492T>C	NP_001309294.1:p.Leu498=
NM_001322366.1:c.1303T>C	NP_001309295.1:p.Leu435=
NM_001322367.1:c.1291T>C	NP_001309296.1:p.Leu431=
NM_001358263.1:c.1399T>C MANE Plus Clinical	NP_001345192.1:p.Leu467=
XM_024447969.1:c.1399T>C	XP_024303737.1:p.Leu467=
NM_000188.3:c.1387T>C MANE Select	NP_000179.2:p.Leu463=
NM_001322364.2:c.1399T>C	NP_001309293.1:p.Leu467=
NM_001322365.2:c.1492T>C	NP_001309294.1:p.Leu498=
NM_033496.3:c.1384T>C	NP_277031.1:p.Leu462=
NM_033497.3:c.1399T>C	NP_277032.1:p.Leu467=
NM_033498.3:c.1399T>C	NP_277033.1:p.Leu467=