Canonical Allele Identifier: CA376909970

Gene: HK1

Linked Data

• gnomAD v4: 10-69382677-G-T
• MyVariant Identifiers: chr10:g.71142433G>T (hg19) ; chr10:g.69382677G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69382677G>T , CM000672.2:g.69382677G>T	GRCh38
NC_000010.10:g.71142433G>T , CM000672.1:g.71142433G>T	GRCh37
NC_000010.9:g.70812439G>T	NCBI36
NG_012077.1:g.117678G>T , LRG_365:g.117678G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470050.2:c.1456G>T	ENSP00000515580.1:p.Glu486Ter
ENST00000703945.1:c.1372G>T	ENSP00000515578.1:p.Glu458Ter
ENST00000703946.1:c.1265+2582G>T	ENSP00000515579.1:n.1265+2582G>T
ENST00000703947.1:c.1066G>T	ENSP00000515581.1:p.Glu356Ter
ENST00000703948.1:c.*1073G>T	ENSP00000515582.1:n.*1073G>T
ENST00000703949.1:c.1456G>T	ENSP00000515583.1:p.Glu486Ter
ENST00000703950.1:c.1456G>T	ENSP00000515584.1:p.Glu486Ter
ENST00000703951.1:c.1265+2582G>T	ENSP00000515585.1:n.1265+2582G>T
ENST00000703952.1:c.1265+2582G>T	ENSP00000515586.1:n.1265+2582G>T
ENST00000703953.1:c.*719G>T	ENSP00000515587.1:n.*719G>T
ENST00000703954.1:c.1336G>T	ENSP00000515588.1:p.Glu446Ter
ENST00000703955.1:n.2006G>T
ENST00000298649.8:c.1453G>T	ENSP00000298649.3:p.Glu485Ter
ENST00000359426.7:c.1456G>T MANE Select	ENSP00000352398.6:p.Glu486Ter
ENST00000436817.6:c.1468G>T	ENSP00000415949.2:p.Glu490Ter
ENST00000493591.6:c.*1344G>T	ENSP00000494917.1:n.*1344G>T
ENST00000643399.2:c.1468G>T MANE Plus Clinical	ENSP00000494664.1:p.Glu490Ter
ENST00000298649.7:c.1453G>T	ENSP00000298649.3:p.Glu485Ter
ENST00000359426.6:c.1456G>T	ENSP00000352398.6:p.Glu486Ter
ENST00000360289.6:c.1420G>T	ENSP00000353433.2:p.Glu474Ter
ENST00000448642.6:c.1468G>T	ENSP00000402103.3:p.Glu490Ter
ENST00000494253.1:n.1682G>T
NM_000188.2:c.1456G>T	NP_000179.2:p.Glu486Ter
NM_033496.2:c.1453G>T	NP_277031.1:p.Glu485Ter
NM_033497.2:c.1468G>T	NP_277032.1:p.Glu490Ter
NM_033498.2:c.1468G>T	NP_277033.1:p.Glu490Ter
NM_033500.2:c.1420G>T , LRG_365t1:c.1420G>T	NP_277035.2:p.Glu474Ter
XM_005269735.2:c.1585G>T	XP_005269792.1:p.Glu529Ter
XM_005269736.1:c.1468G>T	XP_005269793.1:p.Glu490Ter
XM_005269737.1:c.1372G>T	XP_005269794.1:p.Glu458Ter
XM_011539732.1:c.1420G>T	XP_011538034.1:p.Glu474Ter
XM_011539733.1:c.1414G>T	XP_011538035.1:p.Glu472Ter
XM_011539734.1:c.1411G>T	XP_011538036.1:p.Glu471Ter
NM_001322364.1:c.1468G>T	NP_001309293.1:p.Glu490Ter
NM_001322365.1:c.1561G>T	NP_001309294.1:p.Glu521Ter
NM_001322366.1:c.1372G>T	NP_001309295.1:p.Glu458Ter
NM_001322367.1:c.1360G>T	NP_001309296.1:p.Glu454Ter
NM_001358263.1:c.1468G>T MANE Plus Clinical	NP_001345192.1:p.Glu490Ter
XM_024447969.1:c.1468G>T	XP_024303737.1:p.Glu490Ter
NM_000188.3:c.1456G>T MANE Select	NP_000179.2:p.Glu486Ter
NM_001322364.2:c.1468G>T	NP_001309293.1:p.Glu490Ter
NM_001322365.2:c.1561G>T	NP_001309294.1:p.Glu521Ter
NM_033496.3:c.1453G>T	NP_277031.1:p.Glu485Ter
NM_033497.3:c.1468G>T	NP_277032.1:p.Glu490Ter
NM_033498.3:c.1468G>T	NP_277033.1:p.Glu490Ter