Canonical Allele Identifier: CA384555858
Gene: PFKM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48145097A>C , CM000674.2:g.48145097A>C GRCh38
NC_000012.11:g.48538880A>C , CM000674.1:g.48538880A>C GRCh37
NC_000012.10:g.46825147A>C NCBI36
NG_016199.1:g.44225A>C
NG_016199.2:g.44845A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000550257.7:c.2281A>C ENSP00000447997.3:p.Met761Leu
ENST00000340802.12:c.2272A>C ENSP00000345771.6:p.Met758Leu
ENST00000359794.11:c.2059A>C MANE Select ENSP00000352842.5:p.Met687Leu
ENST00000549941.7:c.1801A>C ENSP00000446829.3:p.Met601Leu
ENST00000550345.6:c.2059A>C ENSP00000450369.2:p.Met687Leu
ENST00000550924.6:c.2059A>C ENSP00000446945.2:p.Met687Leu
ENST00000551339.6:c.2059A>C ENSP00000448253.2:p.Met687Leu
ENST00000642730.1:c.2368A>C ENSP00000496597.1:p.Met790Leu
ENST00000312352.11:c.2059A>C ENSP00000309438.7:p.Met687Leu
ENST00000340802.10:c.2272A>C ENSP00000345771.6:p.Met758Leu
ENST00000359794.9:c.2059A>C ENSP00000352842.5:p.Met687Leu
ENST00000546964.5:n.2383A>C
ENST00000547581.5:c.*2327A>C ENSP00000447992.1:n.*2327A>C
ENST00000547587.5:c.2059A>C ENSP00000449426.1:p.Met687Leu
ENST00000551804.5:c.1966A>C ENSP00000448177.1:p.Met656Leu
NM_000289.5:c.2059A>C NP_000280.1:p.Met687Leu
NM_001166686.1:c.2272A>C NP_001160158.1:p.Met758Leu
NM_001166687.1:c.2059A>C NP_001160159.1:p.Met687Leu
NM_001166688.1:c.2059A>C NP_001160160.1:p.Met687Leu
XM_005268974.1:c.2368A>C XP_005269031.1:p.Met790Leu
XM_005268975.1:c.2368A>C XP_005269032.1:p.Met790Leu
XM_005268976.2:c.2368A>C XP_005269033.1:p.Met790Leu
XM_005268977.1:c.2272A>C XP_005269034.1:p.Met758Leu
XM_005268978.2:c.2272A>C XP_005269035.1:p.Met758Leu
XM_005268979.1:c.2272A>C XP_005269036.1:p.Met758Leu
XM_011538487.1:c.2275A>C XP_011536789.1:p.Met759Leu
XM_011538488.1:c.2059A>C XP_011536790.1:p.Met687Leu
NM_000289.6:c.2059A>C MANE Select NP_000280.1:p.Met687Leu
NM_001166686.2:c.2272A>C NP_001160158.1:p.Met758Leu
NM_001354735.1:c.2368A>C NP_001341664.1:p.Met790Leu
NM_001354736.1:c.2368A>C NP_001341665.1:p.Met790Leu
NM_001354737.1:c.2272A>C NP_001341666.1:p.Met758Leu
NM_001354738.1:c.2272A>C NP_001341667.1:p.Met758Leu
NM_001354739.1:c.2272A>C NP_001341668.1:p.Met758Leu
NM_001354740.1:c.2203A>C NP_001341669.1:p.Met735Leu
NM_001354741.1:c.2083A>C NP_001341670.1:p.Met695Leu
NM_001354742.1:c.2059A>C NP_001341671.1:p.Met687Leu
NM_001354743.1:c.2059A>C NP_001341672.1:p.Met687Leu
NM_001354744.1:c.2059A>C NP_001341673.1:p.Met687Leu
NM_001354745.1:c.1972A>C NP_001341674.1:p.Met658Leu
NM_001354746.1:c.1933A>C NP_001341675.1:p.Met645Leu
NM_001354747.1:c.1909A>C NP_001341676.1:p.Met637Leu
NM_001354748.1:c.1909A>C NP_001341677.1:p.Met637Leu
NM_001363619.1:c.1966A>C NP_001350548.1:p.Met656Leu
NR_148954.1:n.2496A>C
NR_148955.1:n.3132A>C
NR_148956.1:n.2422A>C
NR_148957.1:n.2651A>C
NR_148958.1:n.2399A>C
NR_148959.1:n.2325A>C
XM_005268976.3:c.2368A>C XP_005269033.1:p.Met790Leu
XM_017019469.1:c.2179A>C XP_016874958.1:p.Met727Leu
XM_024449020.1:c.2281A>C XP_024304788.1:p.Met761Leu
XM_024449021.1:c.2158A>C XP_024304789.1:p.Met720Leu
XM_024449022.1:c.2059A>C XP_024304790.1:p.Met687Leu
NM_001166687.2:c.2059A>C NP_001160159.1:p.Met687Leu
NM_001166688.2:c.2059A>C NP_001160160.1:p.Met687Leu
NM_001354741.2:c.2083A>C NP_001341670.1:p.Met695Leu
NM_001354742.2:c.2059A>C NP_001341671.1:p.Met687Leu
NM_001354743.2:c.2059A>C NP_001341672.1:p.Met687Leu
NM_001354744.2:c.2059A>C NP_001341673.1:p.Met687Leu
NM_001354745.2:c.1972A>C NP_001341674.1:p.Met658Leu
NM_001354746.2:c.1933A>C NP_001341675.1:p.Met645Leu
NM_001354747.2:c.1909A>C NP_001341676.1:p.Met637Leu
NM_001354748.2:c.1909A>C NP_001341677.1:p.Met637Leu
NM_001363619.2:c.1966A>C NP_001350548.1:p.Met656Leu
NR_148954.2:n.2362A>C
NR_148956.2:n.2288A>C
NR_148957.2:n.2517A>C
NR_148958.2:n.2265A>C
NR_148959.2:n.2191A>C