Canonical Allele Identifier: CA376909789

Gene: HK1

Linked Data

• dbSNP Id: rs1391553871
• gnomAD v2: 10-71142380-G-C
• gnomAD v4: 10-69382624-G-C
• MyVariant Identifiers: chr10:g.71142380G>C (hg19) ; chr10:g.69382624G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69382624G>C , CM000672.2:g.69382624G>C	GRCh38
NC_000010.10:g.71142380G>C , CM000672.1:g.71142380G>C	GRCh37
NC_000010.9:g.70812386G>C	NCBI36
NG_012077.1:g.117625G>C , LRG_365:g.117625G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470050.2:c.1403G>C	ENSP00000515580.1:p.Arg468Pro
ENST00000703945.1:c.1319G>C	ENSP00000515578.1:p.Arg440Pro
ENST00000703946.1:c.1265+2529G>C	ENSP00000515579.1:n.1265+2529G>C
ENST00000703947.1:c.1013G>C	ENSP00000515581.1:p.Arg338Pro
ENST00000703948.1:c.*1020G>C	ENSP00000515582.1:n.*1020G>C
ENST00000703949.1:c.1403G>C	ENSP00000515583.1:p.Arg468Pro
ENST00000703950.1:c.1403G>C	ENSP00000515584.1:p.Arg468Pro
ENST00000703951.1:c.1265+2529G>C	ENSP00000515585.1:n.1265+2529G>C
ENST00000703952.1:c.1265+2529G>C	ENSP00000515586.1:n.1265+2529G>C
ENST00000703953.1:c.*666G>C	ENSP00000515587.1:n.*666G>C
ENST00000703954.1:c.1283G>C	ENSP00000515588.1:p.Arg428Pro
ENST00000703955.1:n.1953G>C
ENST00000298649.8:c.1400G>C	ENSP00000298649.3:p.Arg467Pro
ENST00000359426.7:c.1403G>C MANE Select	ENSP00000352398.6:p.Arg468Pro
ENST00000436817.6:c.1415G>C	ENSP00000415949.2:p.Arg472Pro
ENST00000493591.6:c.*1291G>C	ENSP00000494917.1:n.*1291G>C
ENST00000643399.2:c.1415G>C MANE Plus Clinical	ENSP00000494664.1:p.Arg472Pro
ENST00000298649.7:c.1400G>C	ENSP00000298649.3:p.Arg467Pro
ENST00000359426.6:c.1403G>C	ENSP00000352398.6:p.Arg468Pro
ENST00000360289.6:c.1367G>C	ENSP00000353433.2:p.Arg456Pro
ENST00000448642.6:c.1415G>C	ENSP00000402103.3:p.Arg472Pro
ENST00000494253.1:n.1629G>C
NM_000188.2:c.1403G>C	NP_000179.2:p.Arg468Pro
NM_033496.2:c.1400G>C	NP_277031.1:p.Arg467Pro
NM_033497.2:c.1415G>C	NP_277032.1:p.Arg472Pro
NM_033498.2:c.1415G>C	NP_277033.1:p.Arg472Pro
NM_033500.2:c.1367G>C , LRG_365t1:c.1367G>C	NP_277035.2:p.Arg456Pro
XM_005269735.2:c.1532G>C	XP_005269792.1:p.Arg511Pro
XM_005269736.1:c.1415G>C	XP_005269793.1:p.Arg472Pro
XM_005269737.1:c.1319G>C	XP_005269794.1:p.Arg440Pro
XM_011539732.1:c.1367G>C	XP_011538034.1:p.Arg456Pro
XM_011539733.1:c.1361G>C	XP_011538035.1:p.Arg454Pro
XM_011539734.1:c.1358G>C	XP_011538036.1:p.Arg453Pro
NM_001322364.1:c.1415G>C	NP_001309293.1:p.Arg472Pro
NM_001322365.1:c.1508G>C	NP_001309294.1:p.Arg503Pro
NM_001322366.1:c.1319G>C	NP_001309295.1:p.Arg440Pro
NM_001322367.1:c.1307G>C	NP_001309296.1:p.Arg436Pro
NM_001358263.1:c.1415G>C MANE Plus Clinical	NP_001345192.1:p.Arg472Pro
XM_024447969.1:c.1415G>C	XP_024303737.1:p.Arg472Pro
NM_000188.3:c.1403G>C MANE Select	NP_000179.2:p.Arg468Pro
NM_001322364.2:c.1415G>C	NP_001309293.1:p.Arg472Pro
NM_001322365.2:c.1508G>C	NP_001309294.1:p.Arg503Pro
NM_033496.3:c.1400G>C	NP_277031.1:p.Arg467Pro
NM_033497.3:c.1415G>C	NP_277032.1:p.Arg472Pro
NM_033498.3:c.1415G>C	NP_277033.1:p.Arg472Pro