Canonical Allele Identifier: CA2580085560
Gene: PFKM HGNC NCBI

Linked Data

ClinVar Variation Id: 1725921
ClinVar RCV Id: RCV002306892

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48141820del , CM000674.2:g.48141820del GRCh38
NC_000012.11:g.48535603del , CM000674.1:g.48535603del GRCh37
NC_000012.10:g.46821870del NCBI36
NG_016199.1:g.40948del
NG_016199.2:g.41568del

Transcript Alleles

HGVS Amino-acid Change
ENST00000550257.7:c.1715del ENSP00000447997.3:p.Gly572AlafsTer11
ENST00000340802.12:c.1706del ENSP00000345771.6:p.Gly569AlafsTer11
ENST00000359794.11:c.1493del MANE Select ENSP00000352842.5:p.Gly498AlafsTer11
ENST00000549941.7:c.1400del ENSP00000446829.3:p.Gly467AlafsTer11
ENST00000550345.6:c.1493del ENSP00000450369.2:p.Gly498AlafsTer11
ENST00000550924.6:c.1493del ENSP00000446945.2:p.Gly498AlafsTer11
ENST00000551339.6:c.1493del ENSP00000448253.2:p.Gly498AlafsTer11
ENST00000642730.1:c.1802del ENSP00000496597.1:p.Gly601AlafsTer11
ENST00000312352.11:c.1493del ENSP00000309438.7:p.Gly498AlafsTer11
ENST00000340802.10:c.1706del ENSP00000345771.6:p.Gly569AlafsTer11
ENST00000359794.9:c.1493del ENSP00000352842.5:p.Gly498AlafsTer11
ENST00000546465.1:c.338del ENSP00000446519.1:p.Gly113AlafsTer11
ENST00000546964.5:n.1817del
ENST00000547581.5:c.*1761del ENSP00000447992.1:n.*1761del
ENST00000547587.5:c.1493del ENSP00000449426.1:p.Gly498AlafsTer11
ENST00000550802.1:n.125del
ENST00000551804.5:c.1400del ENSP00000448177.1:p.Gly467AlafsTer11
ENST00000552214.1:n.149del
ENST00000552752.5:c.642del
ENST00000552818.1:n.116del
NM_000289.5:c.1493del NP_000280.1:p.Gly498AlafsTer11
NM_001166686.1:c.1706del NP_001160158.1:p.Gly569AlafsTer11
NM_001166687.1:c.1493del NP_001160159.1:p.Gly498AlafsTer11
NM_001166688.1:c.1493del NP_001160160.1:p.Gly498AlafsTer11
XM_005268974.1:c.1802del XP_005269031.1:p.Gly601AlafsTer11
XM_005268975.1:c.1802del XP_005269032.1:p.Gly601AlafsTer11
XM_005268976.2:c.1802del XP_005269033.1:p.Gly601AlafsTer11
XM_005268977.1:c.1706del XP_005269034.1:p.Gly569AlafsTer11
XM_005268978.2:c.1706del XP_005269035.1:p.Gly569AlafsTer11
XM_005268979.1:c.1706del XP_005269036.1:p.Gly569AlafsTer11
XM_011538487.1:c.1709del XP_011536789.1:p.Gly570AlafsTer11
XM_011538488.1:c.1493del XP_011536790.1:p.Gly498AlafsTer11
NM_000289.6:c.1493del MANE Select NP_000280.1:p.Gly498AlafsTer11
NM_001166686.2:c.1706del NP_001160158.1:p.Gly569AlafsTer11
NM_001354735.1:c.1802del NP_001341664.1:p.Gly601AlafsTer11
NM_001354736.1:c.1802del NP_001341665.1:p.Gly601AlafsTer11
NM_001354737.1:c.1706del NP_001341666.1:p.Gly569AlafsTer11
NM_001354738.1:c.1706del NP_001341667.1:p.Gly569AlafsTer11
NM_001354739.1:c.1706del NP_001341668.1:p.Gly569AlafsTer11
NM_001354740.1:c.1637del NP_001341669.1:p.Gly546AlafsTer11
NM_001354741.1:c.1517del NP_001341670.1:p.Gly506AlafsTer11
NM_001354742.1:c.1493del NP_001341671.1:p.Gly498AlafsTer11
NM_001354743.1:c.1493del NP_001341672.1:p.Gly498AlafsTer11
NM_001354744.1:c.1493del NP_001341673.1:p.Gly498AlafsTer11
NM_001354745.1:c.1406del NP_001341674.1:p.Gly469AlafsTer11
NM_001354746.1:c.1367del NP_001341675.1:p.Gly456AlafsTer11
NM_001354747.1:c.1343del NP_001341676.1:p.Gly448AlafsTer11
NM_001354748.1:c.1343del NP_001341677.1:p.Gly448AlafsTer11
NM_001363619.1:c.1400del NP_001350548.1:p.Gly467AlafsTer11
NR_148954.1:n.1930del
NR_148955.1:n.2566del
NR_148956.1:n.1856del
NR_148957.1:n.2085del
NR_148958.1:n.1833del
NR_148959.1:n.1759del
XM_005268976.3:c.1802del XP_005269033.1:p.Gly601AlafsTer11
XM_017019469.1:c.1613del XP_016874958.1:p.Gly538AlafsTer11
XM_024449020.1:c.1715del XP_024304788.1:p.Gly572AlafsTer11
XM_024449021.1:c.1592del XP_024304789.1:p.Gly531AlafsTer11
XM_024449022.1:c.1493del XP_024304790.1:p.Gly498AlafsTer11
NM_001166687.2:c.1493del NP_001160159.1:p.Gly498AlafsTer11
NM_001166688.2:c.1493del NP_001160160.1:p.Gly498AlafsTer11
NM_001354741.2:c.1517del NP_001341670.1:p.Gly506AlafsTer11
NM_001354742.2:c.1493del NP_001341671.1:p.Gly498AlafsTer11
NM_001354743.2:c.1493del NP_001341672.1:p.Gly498AlafsTer11
NM_001354744.2:c.1493del NP_001341673.1:p.Gly498AlafsTer11
NM_001354745.2:c.1406del NP_001341674.1:p.Gly469AlafsTer11
NM_001354746.2:c.1367del NP_001341675.1:p.Gly456AlafsTer11
NM_001354747.2:c.1343del NP_001341676.1:p.Gly448AlafsTer11
NM_001354748.2:c.1343del NP_001341677.1:p.Gly448AlafsTer11
NM_001363619.2:c.1400del NP_001350548.1:p.Gly467AlafsTer11
NR_148954.2:n.1796del
NR_148956.2:n.1722del
NR_148957.2:n.1951del
NR_148958.2:n.1699del
NR_148959.2:n.1625del