Canonical Allele Identifier: CA376911432

Gene: HK1

Linked Data

• dbSNP Id: rs1839534761
• gnomAD v3: 10-69384462-T-C
• gnomAD v4: 10-69384462-T-C
• MyVariant Identifiers: chr10:g.71144218T>C (hg19) ; chr10:g.69384462T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69384462T>C , CM000672.2:g.69384462T>C	GRCh38
NC_000010.10:g.71144218T>C , CM000672.1:g.71144218T>C	GRCh37
NC_000010.9:g.70814224T>C	NCBI36
NG_012077.1:g.119463T>C , LRG_365:g.119463T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470050.2:c.1700T>C	ENSP00000515580.1:p.Met567Thr
ENST00000703945.1:c.1616T>C	ENSP00000515578.1:p.Met539Thr
ENST00000703946.1:c.1265+4367T>C	ENSP00000515579.1:n.1265+4367T>C
ENST00000703947.1:c.1310T>C	ENSP00000515581.1:p.Met437Thr
ENST00000703948.1:c.*1317T>C	ENSP00000515582.1:n.*1317T>C
ENST00000703949.1:c.1700T>C	ENSP00000515583.1:p.Met567Thr
ENST00000703950.1:c.1700T>C	ENSP00000515584.1:p.Met567Thr
ENST00000703951.1:c.1265+4367T>C	ENSP00000515585.1:n.1265+4367T>C
ENST00000703952.1:c.1265+4367T>C	ENSP00000515586.1:n.1265+4367T>C
ENST00000703953.1:c.*963T>C	ENSP00000515587.1:n.*963T>C
ENST00000703954.1:c.1580T>C	ENSP00000515588.1:p.Met527Thr
ENST00000703955.1:n.2250T>C
ENST00000703957.1:n.205T>C
ENST00000298649.8:c.1697T>C	ENSP00000298649.3:p.Met566Thr
ENST00000359426.7:c.1700T>C MANE Select	ENSP00000352398.6:p.Met567Thr
ENST00000436817.6:c.1712T>C	ENSP00000415949.2:p.Met571Thr
ENST00000493591.6:c.*1588T>C	ENSP00000494917.1:n.*1588T>C
ENST00000643399.2:c.1712T>C MANE Plus Clinical	ENSP00000494664.1:p.Met571Thr
ENST00000298649.7:c.1697T>C	ENSP00000298649.3:p.Met566Thr
ENST00000359426.6:c.1700T>C	ENSP00000352398.6:p.Met567Thr
ENST00000360289.6:c.1664T>C	ENSP00000353433.2:p.Met555Thr
ENST00000448642.6:c.1712T>C	ENSP00000402103.3:p.Met571Thr
ENST00000494253.1:n.1926T>C
NM_000188.2:c.1700T>C	NP_000179.2:p.Met567Thr
NM_033496.2:c.1697T>C	NP_277031.1:p.Met566Thr
NM_033497.2:c.1712T>C	NP_277032.1:p.Met571Thr
NM_033498.2:c.1712T>C	NP_277033.1:p.Met571Thr
NM_033500.2:c.1664T>C , LRG_365t1:c.1664T>C	NP_277035.2:p.Met555Thr
XM_005269735.2:c.1829T>C	XP_005269792.1:p.Met610Thr
XM_005269736.1:c.1712T>C	XP_005269793.1:p.Met571Thr
XM_005269737.1:c.1616T>C	XP_005269794.1:p.Met539Thr
XM_011539732.1:c.1664T>C	XP_011538034.1:p.Met555Thr
XM_011539733.1:c.1658T>C	XP_011538035.1:p.Met553Thr
XM_011539734.1:c.1655T>C	XP_011538036.1:p.Met552Thr
NM_001322364.1:c.1712T>C	NP_001309293.1:p.Met571Thr
NM_001322365.1:c.1805T>C	NP_001309294.1:p.Met602Thr
NM_001322366.1:c.1616T>C	NP_001309295.1:p.Met539Thr
NM_001322367.1:c.1604T>C	NP_001309296.1:p.Met535Thr
NM_001358263.1:c.1712T>C MANE Plus Clinical	NP_001345192.1:p.Met571Thr
XM_024447969.1:c.1712T>C	XP_024303737.1:p.Met571Thr
NM_000188.3:c.1700T>C MANE Select	NP_000179.2:p.Met567Thr
NM_001322364.2:c.1712T>C	NP_001309293.1:p.Met571Thr
NM_001322365.2:c.1805T>C	NP_001309294.1:p.Met602Thr
NM_033496.3:c.1697T>C	NP_277031.1:p.Met566Thr
NM_033497.3:c.1712T>C	NP_277032.1:p.Met571Thr
NM_033498.3:c.1712T>C	NP_277033.1:p.Met571Thr