Canonical Allele Identifier: CA376910814

Gene: HK1

Linked Data

• MyVariant Identifiers: chr10:g.71144090G>C (hg19) ; chr10:g.69384334G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69384334G>C , CM000672.2:g.69384334G>C	GRCh38
NC_000010.10:g.71144090G>C , CM000672.1:g.71144090G>C	GRCh37
NC_000010.9:g.70814096G>C	NCBI36
NG_012077.1:g.119335G>C , LRG_365:g.119335G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470050.2:c.1572G>C	ENSP00000515580.1:p.Glu524Asp
ENST00000703945.1:c.1488G>C	ENSP00000515578.1:p.Glu496Asp
ENST00000703946.1:c.1265+4239G>C	ENSP00000515579.1:n.1265+4239G>C
ENST00000703947.1:c.1182G>C	ENSP00000515581.1:p.Glu394Asp
ENST00000703948.1:c.*1189G>C	ENSP00000515582.1:n.*1189G>C
ENST00000703949.1:c.1572G>C	ENSP00000515583.1:p.Glu524Asp
ENST00000703950.1:c.1572G>C	ENSP00000515584.1:p.Glu524Asp
ENST00000703951.1:c.1265+4239G>C	ENSP00000515585.1:n.1265+4239G>C
ENST00000703952.1:c.1265+4239G>C	ENSP00000515586.1:n.1265+4239G>C
ENST00000703953.1:c.*835G>C	ENSP00000515587.1:n.*835G>C
ENST00000703954.1:c.1452G>C	ENSP00000515588.1:p.Glu484Asp
ENST00000703955.1:n.2122G>C
ENST00000703957.1:n.77G>C
ENST00000298649.8:c.1569G>C	ENSP00000298649.3:p.Glu523Asp
ENST00000359426.7:c.1572G>C MANE Select	ENSP00000352398.6:p.Glu524Asp
ENST00000436817.6:c.1584G>C	ENSP00000415949.2:p.Glu528Asp
ENST00000493591.6:c.*1460G>C	ENSP00000494917.1:n.*1460G>C
ENST00000643399.2:c.1584G>C MANE Plus Clinical	ENSP00000494664.1:p.Glu528Asp
ENST00000298649.7:c.1569G>C	ENSP00000298649.3:p.Glu523Asp
ENST00000359426.6:c.1572G>C	ENSP00000352398.6:p.Glu524Asp
ENST00000360289.6:c.1536G>C	ENSP00000353433.2:p.Glu512Asp
ENST00000448642.6:c.1584G>C	ENSP00000402103.3:p.Glu528Asp
ENST00000494253.1:n.1798G>C
NM_000188.2:c.1572G>C	NP_000179.2:p.Glu524Asp
NM_033496.2:c.1569G>C	NP_277031.1:p.Glu523Asp
NM_033497.2:c.1584G>C	NP_277032.1:p.Glu528Asp
NM_033498.2:c.1584G>C	NP_277033.1:p.Glu528Asp
NM_033500.2:c.1536G>C , LRG_365t1:c.1536G>C	NP_277035.2:p.Glu512Asp
XM_005269735.2:c.1701G>C	XP_005269792.1:p.Glu567Asp
XM_005269736.1:c.1584G>C	XP_005269793.1:p.Glu528Asp
XM_005269737.1:c.1488G>C	XP_005269794.1:p.Glu496Asp
XM_011539732.1:c.1536G>C	XP_011538034.1:p.Glu512Asp
XM_011539733.1:c.1530G>C	XP_011538035.1:p.Glu510Asp
XM_011539734.1:c.1527G>C	XP_011538036.1:p.Glu509Asp
NM_001322364.1:c.1584G>C	NP_001309293.1:p.Glu528Asp
NM_001322365.1:c.1677G>C	NP_001309294.1:p.Glu559Asp
NM_001322366.1:c.1488G>C	NP_001309295.1:p.Glu496Asp
NM_001322367.1:c.1476G>C	NP_001309296.1:p.Glu492Asp
NM_001358263.1:c.1584G>C MANE Plus Clinical	NP_001345192.1:p.Glu528Asp
XM_024447969.1:c.1584G>C	XP_024303737.1:p.Glu528Asp
NM_000188.3:c.1572G>C MANE Select	NP_000179.2:p.Glu524Asp
NM_001322364.2:c.1584G>C	NP_001309293.1:p.Glu528Asp
NM_001322365.2:c.1677G>C	NP_001309294.1:p.Glu559Asp
NM_033496.3:c.1569G>C	NP_277031.1:p.Glu523Asp
NM_033497.3:c.1584G>C	NP_277032.1:p.Glu528Asp
NM_033498.3:c.1584G>C	NP_277033.1:p.Glu528Asp