Canonical Allele Identifier: CA470276343

Gene: HK1

Linked Data

• MyVariant Identifiers: chr10:g.71142255T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69382499T>A , CM000672.2:g.69382499T>A	GRCh38
NC_000010.10:g.71142255T>A , CM000672.1:g.71142255T>A	GRCh37
NC_000010.9:g.70812261T>A	NCBI36
NG_012077.1:g.117500T>A , LRG_365:g.117500T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000470050.2:c.1278T>A	ENSP00000515580.1:p.Arg426=
ENST00000703945.1:c.1194T>A	ENSP00000515578.1:p.Arg398=
ENST00000703946.1:c.1265+2404T>A	ENSP00000515579.1:n.1265+2404T>A
ENST00000703947.1:c.888T>A	ENSP00000515581.1:p.Arg296=
ENST00000703948.1:c.*895T>A	ENSP00000515582.1:n.*895T>A
ENST00000703949.1:c.1278T>A	ENSP00000515583.1:p.Arg426=
ENST00000703950.1:c.1278T>A	ENSP00000515584.1:p.Arg426=
ENST00000703951.1:c.1265+2404T>A	ENSP00000515585.1:n.1265+2404T>A
ENST00000703952.1:c.1265+2404T>A	ENSP00000515586.1:n.1265+2404T>A
ENST00000703953.1:c.*541T>A	ENSP00000515587.1:n.*541T>A
ENST00000703954.1:c.1158T>A	ENSP00000515588.1:p.Arg386=
ENST00000703955.1:n.1828T>A
ENST00000298649.8:c.1275T>A	ENSP00000298649.3:p.Arg425=
ENST00000359426.7:c.1278T>A MANE Select	ENSP00000352398.6:p.Arg426=
ENST00000436817.6:c.1290T>A	ENSP00000415949.2:p.Arg430=
ENST00000493591.6:c.*1166T>A	ENSP00000494917.1:n.*1166T>A
ENST00000643399.2:c.1290T>A MANE Plus Clinical	ENSP00000494664.1:p.Arg430=
ENST00000298649.7:c.1275T>A	ENSP00000298649.3:p.Arg425=
ENST00000359426.6:c.1278T>A	ENSP00000352398.6:p.Arg426=
ENST00000360289.6:c.1242T>A	ENSP00000353433.2:p.Arg414=
ENST00000448642.6:c.1290T>A	ENSP00000402103.3:p.Arg430=
ENST00000494253.1:n.1504T>A
NM_000188.2:c.1278T>A	NP_000179.2:p.Arg426=
NM_033496.2:c.1275T>A	NP_277031.1:p.Arg425=
NM_033497.2:c.1290T>A	NP_277032.1:p.Arg430=
NM_033498.2:c.1290T>A	NP_277033.1:p.Arg430=
NM_033500.2:c.1242T>A , LRG_365t1:c.1242T>A	NP_277035.2:p.Arg414=
XM_005269735.2:c.1407T>A	XP_005269792.1:p.Arg469=
XM_005269736.1:c.1290T>A	XP_005269793.1:p.Arg430=
XM_005269737.1:c.1194T>A	XP_005269794.1:p.Arg398=
XM_011539732.1:c.1242T>A	XP_011538034.1:p.Arg414=
XM_011539733.1:c.1236T>A	XP_011538035.1:p.Arg412=
XM_011539734.1:c.1233T>A	XP_011538036.1:p.Arg411=
NM_001322364.1:c.1290T>A	NP_001309293.1:p.Arg430=
NM_001322365.1:c.1383T>A	NP_001309294.1:p.Arg461=
NM_001322366.1:c.1194T>A	NP_001309295.1:p.Arg398=
NM_001322367.1:c.1182T>A	NP_001309296.1:p.Arg394=
NM_001358263.1:c.1290T>A MANE Plus Clinical	NP_001345192.1:p.Arg430=
XM_024447969.1:c.1290T>A	XP_024303737.1:p.Arg430=
NM_000188.3:c.1278T>A MANE Select	NP_000179.2:p.Arg426=
NM_001322364.2:c.1290T>A	NP_001309293.1:p.Arg430=
NM_001322365.2:c.1383T>A	NP_001309294.1:p.Arg461=
NM_033496.3:c.1275T>A	NP_277031.1:p.Arg425=
NM_033497.3:c.1290T>A	NP_277032.1:p.Arg430=
NM_033498.3:c.1290T>A	NP_277033.1:p.Arg430=