Canonical Allele Identifier: CA2034529185
Gene: PFKM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48132896G= , CM000674.2:g.48132896G= GRCh38
NC_000012.11:g.48526679G= , CM000674.1:g.48526679G= GRCh37
NC_000012.10:g.46812946G= NCBI36
NG_016199.1:g.32024G=
NG_016199.2:g.32644G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000550257.7:c.488G= ENSP00000447997.3:p.Cys163=
ENST00000340802.12:c.479G= ENSP00000345771.6:p.Cys160=
ENST00000359794.11:c.266G= MANE Select ENSP00000352842.5:p.Cys89=
ENST00000549941.7:c.266G= ENSP00000446829.3:p.Cys89=
ENST00000550345.6:c.266G= ENSP00000450369.2:p.Cys89=
ENST00000550924.6:c.266G= ENSP00000446945.2:p.Cys89=
ENST00000551339.6:c.266G= ENSP00000448253.2:p.Cys89=
ENST00000642730.1:c.575G= ENSP00000496597.1:p.Cys192=
ENST00000312352.11:c.266G= ENSP00000309438.7:p.Cys89=
ENST00000340802.10:c.479G= ENSP00000345771.6:p.Cys160=
ENST00000359794.9:c.266G= ENSP00000352842.5:p.Cys89=
ENST00000546465.1:c.86-7875G= ENSP00000446519.1:n.86-7875G=
ENST00000546964.5:n.338G=
ENST00000547581.5:c.*282G= ENSP00000447992.1:n.*282G=
ENST00000547587.5:c.266G= ENSP00000449426.1:p.Cys89=
ENST00000548345.5:c.266G= ENSP00000449269.1:p.Cys89=
ENST00000549003.5:c.266G= ENSP00000449835.1:p.Cys89=
ENST00000549022.5:c.266G= ENSP00000446805.1:p.Cys89=
ENST00000549941.5:c.365G= ENSP00000446829.1:p.Cys122=
ENST00000550345.5:c.266G= ENSP00000450369.1:p.Cys89=
ENST00000551339.5:c.266G= ENSP00000448253.1:p.Cys89=
ENST00000551485.5:c.*150G= ENSP00000448315.1:n.*150G=
ENST00000551804.5:c.266G= ENSP00000448177.1:p.Cys89=
ENST00000552989.5:c.86-1343G= ENSP00000447774.1:n.86-1343G=
NM_000289.5:c.266G= NP_000280.1:p.Cys89=
NM_001166686.1:c.479G= NP_001160158.1:p.Cys160=
NM_001166687.1:c.266G= NP_001160159.1:p.Cys89=
NM_001166688.1:c.266G= NP_001160160.1:p.Cys89=
XM_005268974.1:c.575G= XP_005269031.1:p.Cys192=
XM_005268975.1:c.575G= XP_005269032.1:p.Cys192=
XM_005268976.2:c.575G= XP_005269033.1:p.Cys192=
XM_005268977.1:c.479G= XP_005269034.1:p.Cys160=
XM_005268978.2:c.479G= XP_005269035.1:p.Cys160=
XM_005268979.1:c.479G= XP_005269036.1:p.Cys160=
XM_011538487.1:c.575G= XP_011536789.1:p.Cys192=
XM_011538488.1:c.266G= XP_011536790.1:p.Cys89=
NM_000289.6:c.266G= MANE Select NP_000280.1:p.Cys89=
NM_001166686.2:c.479G= NP_001160158.1:p.Cys160=
NM_001354735.1:c.575G= NP_001341664.1:p.Cys192=
NM_001354736.1:c.575G= NP_001341665.1:p.Cys192=
NM_001354737.1:c.479G= NP_001341666.1:p.Cys160=
NM_001354738.1:c.479G= NP_001341667.1:p.Cys160=
NM_001354739.1:c.479G= NP_001341668.1:p.Cys160=
NM_001354740.1:c.410G= NP_001341669.1:p.Cys137=
NM_001354741.1:c.290G= NP_001341670.1:p.Cys97=
NM_001354742.1:c.266G= NP_001341671.1:p.Cys89=
NM_001354743.1:c.266G= NP_001341672.1:p.Cys89=
NM_001354744.1:c.266G= NP_001341673.1:p.Cys89=
NM_001354745.1:c.179G= NP_001341674.1:p.Cys60=
NM_001354746.1:c.266G= NP_001341675.1:p.Cys89=
NM_001354747.1:c.116G= NP_001341676.1:p.Cys39=
NM_001354748.1:c.116G= NP_001341677.1:p.Cys39=
NM_001363619.1:c.266G= NP_001350548.1:p.Cys89=
NR_148954.1:n.451G=
NR_148955.1:n.1087G=
NR_148956.1:n.377G=
NR_148957.1:n.451G=
NR_148958.1:n.451G=
NR_148959.1:n.377G=
XM_005268976.3:c.575G= XP_005269033.1:p.Cys192=
XM_017019469.1:c.479G= XP_016874958.1:p.Cys160=
XM_024449020.1:c.488G= XP_024304788.1:p.Cys163=
XM_024449021.1:c.365G= XP_024304789.1:p.Cys122=
XM_024449022.1:c.266G= XP_024304790.1:p.Cys89=
NM_001166687.2:c.266G= NP_001160159.1:p.Cys89=
NM_001166688.2:c.266G= NP_001160160.1:p.Cys89=
NM_001354741.2:c.290G= NP_001341670.1:p.Cys97=
NM_001354742.2:c.266G= NP_001341671.1:p.Cys89=
NM_001354743.2:c.266G= NP_001341672.1:p.Cys89=
NM_001354744.2:c.266G= NP_001341673.1:p.Cys89=
NM_001354745.2:c.179G= NP_001341674.1:p.Cys60=
NM_001354746.2:c.266G= NP_001341675.1:p.Cys89=
NM_001354747.2:c.116G= NP_001341676.1:p.Cys39=
NM_001354748.2:c.116G= NP_001341677.1:p.Cys39=
NM_001363619.2:c.266G= NP_001350548.1:p.Cys89=
NR_148954.2:n.317G=
NR_148956.2:n.243G=
NR_148957.2:n.317G=
NR_148958.2:n.317G=
NR_148959.2:n.243G=