Canonical Allele Identifier: CA470027261

Gene: HK1

Linked Data

• MyVariant Identifiers: chr10:g.71144177G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69384421G>C , CM000672.2:g.69384421G>C	GRCh38
NC_000010.10:g.71144177G>C , CM000672.1:g.71144177G>C	GRCh37
NC_000010.9:g.70814183G>C	NCBI36
NG_012077.1:g.119422G>C , LRG_365:g.119422G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470050.2:c.1659G>C	ENSP00000515580.1:p.Val553=
ENST00000703945.1:c.1575G>C	ENSP00000515578.1:p.Val525=
ENST00000703946.1:c.1265+4326G>C	ENSP00000515579.1:n.1265+4326G>C
ENST00000703947.1:c.1269G>C	ENSP00000515581.1:p.Val423=
ENST00000703948.1:c.*1276G>C	ENSP00000515582.1:n.*1276G>C
ENST00000703949.1:c.1659G>C	ENSP00000515583.1:p.Val553=
ENST00000703950.1:c.1659G>C	ENSP00000515584.1:p.Val553=
ENST00000703951.1:c.1265+4326G>C	ENSP00000515585.1:n.1265+4326G>C
ENST00000703952.1:c.1265+4326G>C	ENSP00000515586.1:n.1265+4326G>C
ENST00000703953.1:c.*922G>C	ENSP00000515587.1:n.*922G>C
ENST00000703954.1:c.1539G>C	ENSP00000515588.1:p.Val513=
ENST00000703955.1:n.2209G>C
ENST00000703957.1:n.164G>C
ENST00000298649.8:c.1656G>C	ENSP00000298649.3:p.Val552=
ENST00000359426.7:c.1659G>C MANE Select	ENSP00000352398.6:p.Val553=
ENST00000436817.6:c.1671G>C	ENSP00000415949.2:p.Val557=
ENST00000493591.6:c.*1547G>C	ENSP00000494917.1:n.*1547G>C
ENST00000643399.2:c.1671G>C MANE Plus Clinical	ENSP00000494664.1:p.Val557=
ENST00000298649.7:c.1656G>C	ENSP00000298649.3:p.Val552=
ENST00000359426.6:c.1659G>C	ENSP00000352398.6:p.Val553=
ENST00000360289.6:c.1623G>C	ENSP00000353433.2:p.Val541=
ENST00000448642.6:c.1671G>C	ENSP00000402103.3:p.Val557=
ENST00000494253.1:n.1885G>C
NM_000188.2:c.1659G>C	NP_000179.2:p.Val553=
NM_033496.2:c.1656G>C	NP_277031.1:p.Val552=
NM_033497.2:c.1671G>C	NP_277032.1:p.Val557=
NM_033498.2:c.1671G>C	NP_277033.1:p.Val557=
NM_033500.2:c.1623G>C , LRG_365t1:c.1623G>C	NP_277035.2:p.Val541=
XM_005269735.2:c.1788G>C	XP_005269792.1:p.Val596=
XM_005269736.1:c.1671G>C	XP_005269793.1:p.Val557=
XM_005269737.1:c.1575G>C	XP_005269794.1:p.Val525=
XM_011539732.1:c.1623G>C	XP_011538034.1:p.Val541=
XM_011539733.1:c.1617G>C	XP_011538035.1:p.Val539=
XM_011539734.1:c.1614G>C	XP_011538036.1:p.Val538=
NM_001322364.1:c.1671G>C	NP_001309293.1:p.Val557=
NM_001322365.1:c.1764G>C	NP_001309294.1:p.Val588=
NM_001322366.1:c.1575G>C	NP_001309295.1:p.Val525=
NM_001322367.1:c.1563G>C	NP_001309296.1:p.Val521=
NM_001358263.1:c.1671G>C MANE Plus Clinical	NP_001345192.1:p.Val557=
XM_024447969.1:c.1671G>C	XP_024303737.1:p.Val557=
NM_000188.3:c.1659G>C MANE Select	NP_000179.2:p.Val553=
NM_001322364.2:c.1671G>C	NP_001309293.1:p.Val557=
NM_001322365.2:c.1764G>C	NP_001309294.1:p.Val588=
NM_033496.3:c.1656G>C	NP_277031.1:p.Val552=
NM_033497.3:c.1671G>C	NP_277032.1:p.Val557=
NM_033498.3:c.1671G>C	NP_277033.1:p.Val557=