Canonical Allele Identifier: CA2034538766
Gene: PFKM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48141751A= , CM000674.2:g.48141751A= GRCh38
NC_000012.11:g.48535534A= , CM000674.1:g.48535534A= GRCh37
NC_000012.10:g.46821801A= NCBI36
NG_016199.1:g.40879A=
NG_016199.2:g.41499A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000550257.7:c.1646A= ENSP00000447997.3:p.Lys549=
ENST00000340802.12:c.1637A= ENSP00000345771.6:p.Lys546=
ENST00000359794.11:c.1424A= MANE Select ENSP00000352842.5:p.Lys475=
ENST00000549941.7:c.1331A= ENSP00000446829.3:p.Lys444=
ENST00000550345.6:c.1424A= ENSP00000450369.2:p.Lys475=
ENST00000550924.6:c.1424A= ENSP00000446945.2:p.Lys475=
ENST00000551339.6:c.1424A= ENSP00000448253.2:p.Lys475=
ENST00000642730.1:c.1733A= ENSP00000496597.1:p.Lys578=
ENST00000312352.11:c.1424A= ENSP00000309438.7:p.Lys475=
ENST00000340802.10:c.1637A= ENSP00000345771.6:p.Lys546=
ENST00000359794.9:c.1424A= ENSP00000352842.5:p.Lys475=
ENST00000546465.1:c.269A= ENSP00000446519.1:p.Lys90=
ENST00000546964.5:n.1748A=
ENST00000547581.5:c.*1692A= ENSP00000447992.1:n.*1692A=
ENST00000547587.5:c.1424A= ENSP00000449426.1:p.Lys475=
ENST00000550802.1:n.56A=
ENST00000551804.5:c.1331A= ENSP00000448177.1:p.Lys444=
ENST00000552214.1:n.80A=
ENST00000552752.5:c.573A=
ENST00000552818.1:n.47A=
NM_000289.5:c.1424A= NP_000280.1:p.Lys475=
NM_001166686.1:c.1637A= NP_001160158.1:p.Lys546=
NM_001166687.1:c.1424A= NP_001160159.1:p.Lys475=
NM_001166688.1:c.1424A= NP_001160160.1:p.Lys475=
XM_005268974.1:c.1733A= XP_005269031.1:p.Lys578=
XM_005268975.1:c.1733A= XP_005269032.1:p.Lys578=
XM_005268976.2:c.1733A= XP_005269033.1:p.Lys578=
XM_005268977.1:c.1637A= XP_005269034.1:p.Lys546=
XM_005268978.2:c.1637A= XP_005269035.1:p.Lys546=
XM_005268979.1:c.1637A= XP_005269036.1:p.Lys546=
XM_011538487.1:c.1640A= XP_011536789.1:p.Lys547=
XM_011538488.1:c.1424A= XP_011536790.1:p.Lys475=
NM_000289.6:c.1424A= MANE Select NP_000280.1:p.Lys475=
NM_001166686.2:c.1637A= NP_001160158.1:p.Lys546=
NM_001354735.1:c.1733A= NP_001341664.1:p.Lys578=
NM_001354736.1:c.1733A= NP_001341665.1:p.Lys578=
NM_001354737.1:c.1637A= NP_001341666.1:p.Lys546=
NM_001354738.1:c.1637A= NP_001341667.1:p.Lys546=
NM_001354739.1:c.1637A= NP_001341668.1:p.Lys546=
NM_001354740.1:c.1568A= NP_001341669.1:p.Lys523=
NM_001354741.1:c.1448A= NP_001341670.1:p.Lys483=
NM_001354742.1:c.1424A= NP_001341671.1:p.Lys475=
NM_001354743.1:c.1424A= NP_001341672.1:p.Lys475=
NM_001354744.1:c.1424A= NP_001341673.1:p.Lys475=
NM_001354745.1:c.1337A= NP_001341674.1:p.Lys446=
NM_001354746.1:c.1298A= NP_001341675.1:p.Lys433=
NM_001354747.1:c.1274A= NP_001341676.1:p.Lys425=
NM_001354748.1:c.1274A= NP_001341677.1:p.Lys425=
NM_001363619.1:c.1331A= NP_001350548.1:p.Lys444=
NR_148954.1:n.1861A=
NR_148955.1:n.2497A=
NR_148956.1:n.1787A=
NR_148957.1:n.2016A=
NR_148958.1:n.1764A=
NR_148959.1:n.1690A=
XM_005268976.3:c.1733A= XP_005269033.1:p.Lys578=
XM_017019469.1:c.1544A= XP_016874958.1:p.Lys515=
XM_024449020.1:c.1646A= XP_024304788.1:p.Lys549=
XM_024449021.1:c.1523A= XP_024304789.1:p.Lys508=
XM_024449022.1:c.1424A= XP_024304790.1:p.Lys475=
NM_001166687.2:c.1424A= NP_001160159.1:p.Lys475=
NM_001166688.2:c.1424A= NP_001160160.1:p.Lys475=
NM_001354741.2:c.1448A= NP_001341670.1:p.Lys483=
NM_001354742.2:c.1424A= NP_001341671.1:p.Lys475=
NM_001354743.2:c.1424A= NP_001341672.1:p.Lys475=
NM_001354744.2:c.1424A= NP_001341673.1:p.Lys475=
NM_001354745.2:c.1337A= NP_001341674.1:p.Lys446=
NM_001354746.2:c.1298A= NP_001341675.1:p.Lys433=
NM_001354747.2:c.1274A= NP_001341676.1:p.Lys425=
NM_001354748.2:c.1274A= NP_001341677.1:p.Lys425=
NM_001363619.2:c.1331A= NP_001350548.1:p.Lys444=
NR_148954.2:n.1727A=
NR_148956.2:n.1653A=
NR_148957.2:n.1882A=
NR_148958.2:n.1630A=
NR_148959.2:n.1556A=