Canonical Allele Identifier: CA2034544892
Gene: PFKM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48145040C= , CM000674.2:g.48145040C= GRCh38
NC_000012.11:g.48538823C= , CM000674.1:g.48538823C= GRCh37
NC_000012.10:g.46825090C= NCBI36
NG_016199.1:g.44168C=
NG_016199.2:g.44788C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000550257.7:c.2224C= ENSP00000447997.3:p.Pro742=
ENST00000340802.12:c.2215C= ENSP00000345771.6:p.Pro739=
ENST00000359794.11:c.2002C= MANE Select ENSP00000352842.5:p.Pro668=
ENST00000549941.7:c.1744C= ENSP00000446829.3:p.Pro582=
ENST00000550345.6:c.2002C= ENSP00000450369.2:p.Pro668=
ENST00000550924.6:c.2002C= ENSP00000446945.2:p.Pro668=
ENST00000551339.6:c.2002C= ENSP00000448253.2:p.Pro668=
ENST00000642730.1:c.2311C= ENSP00000496597.1:p.Pro771=
ENST00000312352.11:c.2002C= ENSP00000309438.7:p.Pro668=
ENST00000340802.10:c.2215C= ENSP00000345771.6:p.Pro739=
ENST00000359794.9:c.2002C= ENSP00000352842.5:p.Pro668=
ENST00000546964.5:n.2326C=
ENST00000547581.5:c.*2270C= ENSP00000447992.1:n.*2270C=
ENST00000547587.5:c.2002C= ENSP00000449426.1:p.Pro668=
ENST00000551804.5:c.1909C= ENSP00000448177.1:p.Pro637=
ENST00000553055.1:c.278C=
NM_000289.5:c.2002C= NP_000280.1:p.Pro668=
NM_001166686.1:c.2215C= NP_001160158.1:p.Pro739=
NM_001166687.1:c.2002C= NP_001160159.1:p.Pro668=
NM_001166688.1:c.2002C= NP_001160160.1:p.Pro668=
XM_005268974.1:c.2311C= XP_005269031.1:p.Pro771=
XM_005268975.1:c.2311C= XP_005269032.1:p.Pro771=
XM_005268976.2:c.2311C= XP_005269033.1:p.Pro771=
XM_005268977.1:c.2215C= XP_005269034.1:p.Pro739=
XM_005268978.2:c.2215C= XP_005269035.1:p.Pro739=
XM_005268979.1:c.2215C= XP_005269036.1:p.Pro739=
XM_011538487.1:c.2218C= XP_011536789.1:p.Pro740=
XM_011538488.1:c.2002C= XP_011536790.1:p.Pro668=
NM_000289.6:c.2002C= MANE Select NP_000280.1:p.Pro668=
NM_001166686.2:c.2215C= NP_001160158.1:p.Pro739=
NM_001354735.1:c.2311C= NP_001341664.1:p.Pro771=
NM_001354736.1:c.2311C= NP_001341665.1:p.Pro771=
NM_001354737.1:c.2215C= NP_001341666.1:p.Pro739=
NM_001354738.1:c.2215C= NP_001341667.1:p.Pro739=
NM_001354739.1:c.2215C= NP_001341668.1:p.Pro739=
NM_001354740.1:c.2146C= NP_001341669.1:p.Pro716=
NM_001354741.1:c.2026C= NP_001341670.1:p.Pro676=
NM_001354742.1:c.2002C= NP_001341671.1:p.Pro668=
NM_001354743.1:c.2002C= NP_001341672.1:p.Pro668=
NM_001354744.1:c.2002C= NP_001341673.1:p.Pro668=
NM_001354745.1:c.1915C= NP_001341674.1:p.Pro639=
NM_001354746.1:c.1876C= NP_001341675.1:p.Pro626=
NM_001354747.1:c.1852C= NP_001341676.1:p.Pro618=
NM_001354748.1:c.1852C= NP_001341677.1:p.Pro618=
NM_001363619.1:c.1909C= NP_001350548.1:p.Pro637=
NR_148954.1:n.2439C=
NR_148955.1:n.3075C=
NR_148956.1:n.2365C=
NR_148957.1:n.2594C=
NR_148958.1:n.2342C=
NR_148959.1:n.2268C=
XM_005268976.3:c.2311C= XP_005269033.1:p.Pro771=
XM_017019469.1:c.2122C= XP_016874958.1:p.Pro708=
XM_024449020.1:c.2224C= XP_024304788.1:p.Pro742=
XM_024449021.1:c.2101C= XP_024304789.1:p.Pro701=
XM_024449022.1:c.2002C= XP_024304790.1:p.Pro668=
NM_001166687.2:c.2002C= NP_001160159.1:p.Pro668=
NM_001166688.2:c.2002C= NP_001160160.1:p.Pro668=
NM_001354741.2:c.2026C= NP_001341670.1:p.Pro676=
NM_001354742.2:c.2002C= NP_001341671.1:p.Pro668=
NM_001354743.2:c.2002C= NP_001341672.1:p.Pro668=
NM_001354744.2:c.2002C= NP_001341673.1:p.Pro668=
NM_001354745.2:c.1915C= NP_001341674.1:p.Pro639=
NM_001354746.2:c.1876C= NP_001341675.1:p.Pro626=
NM_001354747.2:c.1852C= NP_001341676.1:p.Pro618=
NM_001354748.2:c.1852C= NP_001341677.1:p.Pro618=
NM_001363619.2:c.1909C= NP_001350548.1:p.Pro637=
NR_148954.2:n.2305C=
NR_148956.2:n.2231C=
NR_148957.2:n.2460C=
NR_148958.2:n.2208C=
NR_148959.2:n.2134C=