Canonical Allele Identifier: CA2034538754
Gene: PFKM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48141741A= , CM000674.2:g.48141741A= GRCh38
NC_000012.11:g.48535524A= , CM000674.1:g.48535524A= GRCh37
NC_000012.10:g.46821791A= NCBI36
NG_016199.1:g.40869A=
NG_016199.2:g.41489A=

Transcript Alleles

HGVS Amino-acid change
ENST00000550257.7:c.1636A= ENSP00000447997.3:p.Thr546=
ENST00000340802.12:c.1627A= ENSP00000345771.6:p.Thr543=
ENST00000359794.11:c.1414A= MANE Select ENSP00000352842.5:p.Thr472=
ENST00000549941.7:c.1321A= ENSP00000446829.3:p.Thr441=
ENST00000550345.6:c.1414A= ENSP00000450369.2:p.Thr472=
ENST00000550924.6:c.1414A= ENSP00000446945.2:p.Thr472=
ENST00000551339.6:c.1414A= ENSP00000448253.2:p.Thr472=
ENST00000642730.1:c.1723A= ENSP00000496597.1:p.Thr575=
ENST00000312352.11:c.1414A= ENSP00000309438.7:p.Thr472=
ENST00000340802.10:c.1627A= ENSP00000345771.6:p.Thr543=
ENST00000359794.9:c.1414A= ENSP00000352842.5:p.Thr472=
ENST00000546465.1:c.259A= ENSP00000446519.1:p.Thr87=
ENST00000546964.5:n.1738A=
ENST00000547581.5:c.*1682A= ENSP00000447992.1:n.*1682A=
ENST00000547587.5:c.1414A= ENSP00000449426.1:p.Thr472=
ENST00000550802.1:n.46A=
ENST00000551804.5:c.1321A= ENSP00000448177.1:p.Thr441=
ENST00000552214.1:n.70A=
ENST00000552752.5:c.563A=
ENST00000552818.1:n.37A=
NM_000289.5:c.1414A= NP_000280.1:p.Thr472=
NM_001166686.1:c.1627A= NP_001160158.1:p.Thr543=
NM_001166687.1:c.1414A= NP_001160159.1:p.Thr472=
NM_001166688.1:c.1414A= NP_001160160.1:p.Thr472=
XM_005268974.1:c.1723A= XP_005269031.1:p.Thr575=
XM_005268975.1:c.1723A= XP_005269032.1:p.Thr575=
XM_005268976.2:c.1723A= XP_005269033.1:p.Thr575=
XM_005268977.1:c.1627A= XP_005269034.1:p.Thr543=
XM_005268978.2:c.1627A= XP_005269035.1:p.Thr543=
XM_005268979.1:c.1627A= XP_005269036.1:p.Thr543=
XM_011538487.1:c.1630A= XP_011536789.1:p.Thr544=
XM_011538488.1:c.1414A= XP_011536790.1:p.Thr472=
NM_000289.6:c.1414A= MANE Select NP_000280.1:p.Thr472=
NM_001166686.2:c.1627A= NP_001160158.1:p.Thr543=
NM_001354735.1:c.1723A= NP_001341664.1:p.Thr575=
NM_001354736.1:c.1723A= NP_001341665.1:p.Thr575=
NM_001354737.1:c.1627A= NP_001341666.1:p.Thr543=
NM_001354738.1:c.1627A= NP_001341667.1:p.Thr543=
NM_001354739.1:c.1627A= NP_001341668.1:p.Thr543=
NM_001354740.1:c.1558A= NP_001341669.1:p.Thr520=
NM_001354741.1:c.1438A= NP_001341670.1:p.Thr480=
NM_001354742.1:c.1414A= NP_001341671.1:p.Thr472=
NM_001354743.1:c.1414A= NP_001341672.1:p.Thr472=
NM_001354744.1:c.1414A= NP_001341673.1:p.Thr472=
NM_001354745.1:c.1327A= NP_001341674.1:p.Thr443=
NM_001354746.1:c.1288A= NP_001341675.1:p.Thr430=
NM_001354747.1:c.1264A= NP_001341676.1:p.Thr422=
NM_001354748.1:c.1264A= NP_001341677.1:p.Thr422=
NM_001363619.1:c.1321A= NP_001350548.1:p.Thr441=
NR_148954.1:n.1851A=
NR_148955.1:n.2487A=
NR_148956.1:n.1777A=
NR_148957.1:n.2006A=
NR_148958.1:n.1754A=
NR_148959.1:n.1680A=
XM_005268976.3:c.1723A= XP_005269033.1:p.Thr575=
XM_017019469.1:c.1534A= XP_016874958.1:p.Thr512=
XM_024449020.1:c.1636A= XP_024304788.1:p.Thr546=
XM_024449021.1:c.1513A= XP_024304789.1:p.Thr505=
XM_024449022.1:c.1414A= XP_024304790.1:p.Thr472=
NM_001166687.2:c.1414A= NP_001160159.1:p.Thr472=
NM_001166688.2:c.1414A= NP_001160160.1:p.Thr472=
NM_001354741.2:c.1438A= NP_001341670.1:p.Thr480=
NM_001354742.2:c.1414A= NP_001341671.1:p.Thr472=
NM_001354743.2:c.1414A= NP_001341672.1:p.Thr472=
NM_001354744.2:c.1414A= NP_001341673.1:p.Thr472=
NM_001354745.2:c.1327A= NP_001341674.1:p.Thr443=
NM_001354746.2:c.1288A= NP_001341675.1:p.Thr430=
NM_001354747.2:c.1264A= NP_001341676.1:p.Thr422=
NM_001354748.2:c.1264A= NP_001341677.1:p.Thr422=
NM_001363619.2:c.1321A= NP_001350548.1:p.Thr441=
NR_148954.2:n.1717A=
NR_148956.2:n.1643A=
NR_148957.2:n.1872A=
NR_148958.2:n.1620A=
NR_148959.2:n.1546A=