Canonical Allele Identifier: CA376910887

Gene: HK1

Linked Data

• MyVariant Identifiers: chr10:g.71144098A>C (hg19) ; chr10:g.69384342A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69384342A>C , CM000672.2:g.69384342A>C	GRCh38
NC_000010.10:g.71144098A>C , CM000672.1:g.71144098A>C	GRCh37
NC_000010.9:g.70814104A>C	NCBI36
NG_012077.1:g.119343A>C , LRG_365:g.119343A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470050.2:c.1580A>C	ENSP00000515580.1:p.Asp527Ala
ENST00000703945.1:c.1496A>C	ENSP00000515578.1:p.Asp499Ala
ENST00000703946.1:c.1265+4247A>C	ENSP00000515579.1:n.1265+4247A>C
ENST00000703947.1:c.1190A>C	ENSP00000515581.1:p.Asp397Ala
ENST00000703948.1:c.*1197A>C	ENSP00000515582.1:n.*1197A>C
ENST00000703949.1:c.1580A>C	ENSP00000515583.1:p.Asp527Ala
ENST00000703950.1:c.1580A>C	ENSP00000515584.1:p.Asp527Ala
ENST00000703951.1:c.1265+4247A>C	ENSP00000515585.1:n.1265+4247A>C
ENST00000703952.1:c.1265+4247A>C	ENSP00000515586.1:n.1265+4247A>C
ENST00000703953.1:c.*843A>C	ENSP00000515587.1:n.*843A>C
ENST00000703954.1:c.1460A>C	ENSP00000515588.1:p.Asp487Ala
ENST00000703955.1:n.2130A>C
ENST00000703957.1:n.85A>C
ENST00000298649.8:c.1577A>C	ENSP00000298649.3:p.Asp526Ala
ENST00000359426.7:c.1580A>C MANE Select	ENSP00000352398.6:p.Asp527Ala
ENST00000436817.6:c.1592A>C	ENSP00000415949.2:p.Asp531Ala
ENST00000493591.6:c.*1468A>C	ENSP00000494917.1:n.*1468A>C
ENST00000643399.2:c.1592A>C MANE Plus Clinical	ENSP00000494664.1:p.Asp531Ala
ENST00000298649.7:c.1577A>C	ENSP00000298649.3:p.Asp526Ala
ENST00000359426.6:c.1580A>C	ENSP00000352398.6:p.Asp527Ala
ENST00000360289.6:c.1544A>C	ENSP00000353433.2:p.Asp515Ala
ENST00000448642.6:c.1592A>C	ENSP00000402103.3:p.Asp531Ala
ENST00000494253.1:n.1806A>C
NM_000188.2:c.1580A>C	NP_000179.2:p.Asp527Ala
NM_033496.2:c.1577A>C	NP_277031.1:p.Asp526Ala
NM_033497.2:c.1592A>C	NP_277032.1:p.Asp531Ala
NM_033498.2:c.1592A>C	NP_277033.1:p.Asp531Ala
NM_033500.2:c.1544A>C , LRG_365t1:c.1544A>C	NP_277035.2:p.Asp515Ala
XM_005269735.2:c.1709A>C	XP_005269792.1:p.Asp570Ala
XM_005269736.1:c.1592A>C	XP_005269793.1:p.Asp531Ala
XM_005269737.1:c.1496A>C	XP_005269794.1:p.Asp499Ala
XM_011539732.1:c.1544A>C	XP_011538034.1:p.Asp515Ala
XM_011539733.1:c.1538A>C	XP_011538035.1:p.Asp513Ala
XM_011539734.1:c.1535A>C	XP_011538036.1:p.Asp512Ala
NM_001322364.1:c.1592A>C	NP_001309293.1:p.Asp531Ala
NM_001322365.1:c.1685A>C	NP_001309294.1:p.Asp562Ala
NM_001322366.1:c.1496A>C	NP_001309295.1:p.Asp499Ala
NM_001322367.1:c.1484A>C	NP_001309296.1:p.Asp495Ala
NM_001358263.1:c.1592A>C MANE Plus Clinical	NP_001345192.1:p.Asp531Ala
XM_024447969.1:c.1592A>C	XP_024303737.1:p.Asp531Ala
NM_000188.3:c.1580A>C MANE Select	NP_000179.2:p.Asp527Ala
NM_001322364.2:c.1592A>C	NP_001309293.1:p.Asp531Ala
NM_001322365.2:c.1685A>C	NP_001309294.1:p.Asp562Ala
NM_033496.3:c.1577A>C	NP_277031.1:p.Asp526Ala
NM_033497.3:c.1592A>C	NP_277032.1:p.Asp531Ala
NM_033498.3:c.1592A>C	NP_277033.1:p.Asp531Ala