Canonical Allele Identifier: CA376909536

Gene: HK1

Linked Data

• MyVariant Identifiers: chr10:g.71142262A>C (hg19) ; chr10:g.69382506A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69382506A>C , CM000672.2:g.69382506A>C	GRCh38
NC_000010.10:g.71142262A>C , CM000672.1:g.71142262A>C	GRCh37
NC_000010.9:g.70812268A>C	NCBI36
NG_012077.1:g.117507A>C , LRG_365:g.117507A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000470050.2:c.1285A>C	ENSP00000515580.1:p.Lys429Gln
ENST00000703945.1:c.1201A>C	ENSP00000515578.1:p.Lys401Gln
ENST00000703946.1:c.1265+2411A>C	ENSP00000515579.1:n.1265+2411A>C
ENST00000703947.1:c.895A>C	ENSP00000515581.1:p.Lys299Gln
ENST00000703948.1:c.*902A>C	ENSP00000515582.1:n.*902A>C
ENST00000703949.1:c.1285A>C	ENSP00000515583.1:p.Lys429Gln
ENST00000703950.1:c.1285A>C	ENSP00000515584.1:p.Lys429Gln
ENST00000703951.1:c.1265+2411A>C	ENSP00000515585.1:n.1265+2411A>C
ENST00000703952.1:c.1265+2411A>C	ENSP00000515586.1:n.1265+2411A>C
ENST00000703953.1:c.*548A>C	ENSP00000515587.1:n.*548A>C
ENST00000703954.1:c.1165A>C	ENSP00000515588.1:p.Lys389Gln
ENST00000703955.1:n.1835A>C
ENST00000298649.8:c.1282A>C	ENSP00000298649.3:p.Lys428Gln
ENST00000359426.7:c.1285A>C MANE Select	ENSP00000352398.6:p.Lys429Gln
ENST00000436817.6:c.1297A>C	ENSP00000415949.2:p.Lys433Gln
ENST00000493591.6:c.*1173A>C	ENSP00000494917.1:n.*1173A>C
ENST00000643399.2:c.1297A>C MANE Plus Clinical	ENSP00000494664.1:p.Lys433Gln
ENST00000298649.7:c.1282A>C	ENSP00000298649.3:p.Lys428Gln
ENST00000359426.6:c.1285A>C	ENSP00000352398.6:p.Lys429Gln
ENST00000360289.6:c.1249A>C	ENSP00000353433.2:p.Lys417Gln
ENST00000448642.6:c.1297A>C	ENSP00000402103.3:p.Lys433Gln
ENST00000494253.1:n.1511A>C
NM_000188.2:c.1285A>C	NP_000179.2:p.Lys429Gln
NM_033496.2:c.1282A>C	NP_277031.1:p.Lys428Gln
NM_033497.2:c.1297A>C	NP_277032.1:p.Lys433Gln
NM_033498.2:c.1297A>C	NP_277033.1:p.Lys433Gln
NM_033500.2:c.1249A>C , LRG_365t1:c.1249A>C	NP_277035.2:p.Lys417Gln
XM_005269735.2:c.1414A>C	XP_005269792.1:p.Lys472Gln
XM_005269736.1:c.1297A>C	XP_005269793.1:p.Lys433Gln
XM_005269737.1:c.1201A>C	XP_005269794.1:p.Lys401Gln
XM_011539732.1:c.1249A>C	XP_011538034.1:p.Lys417Gln
XM_011539733.1:c.1243A>C	XP_011538035.1:p.Lys415Gln
XM_011539734.1:c.1240A>C	XP_011538036.1:p.Lys414Gln
NM_001322364.1:c.1297A>C	NP_001309293.1:p.Lys433Gln
NM_001322365.1:c.1390A>C	NP_001309294.1:p.Lys464Gln
NM_001322366.1:c.1201A>C	NP_001309295.1:p.Lys401Gln
NM_001322367.1:c.1189A>C	NP_001309296.1:p.Lys397Gln
NM_001358263.1:c.1297A>C MANE Plus Clinical	NP_001345192.1:p.Lys433Gln
XM_024447969.1:c.1297A>C	XP_024303737.1:p.Lys433Gln
NM_000188.3:c.1285A>C MANE Select	NP_000179.2:p.Lys429Gln
NM_001322364.2:c.1297A>C	NP_001309293.1:p.Lys433Gln
NM_001322365.2:c.1390A>C	NP_001309294.1:p.Lys464Gln
NM_033496.3:c.1282A>C	NP_277031.1:p.Lys428Gln
NM_033497.3:c.1297A>C	NP_277032.1:p.Lys433Gln
NM_033498.3:c.1297A>C	NP_277033.1:p.Lys433Gln