Canonical Allele Identifier: CA2034538782
Gene: PFKM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48141766A= , CM000674.2:g.48141766A= GRCh38
NC_000012.11:g.48535549A= , CM000674.1:g.48535549A= GRCh37
NC_000012.10:g.46821816A= NCBI36
NG_016199.1:g.40894A=
NG_016199.2:g.41514A=

Transcript Alleles

HGVS Amino-acid change
ENST00000550257.7:c.1661A= ENSP00000447997.3:p.Gln554=
ENST00000340802.12:c.1652A= ENSP00000345771.6:p.Gln551=
ENST00000359794.11:c.1439A= MANE Select ENSP00000352842.5:p.Gln480=
ENST00000549941.7:c.1346A= ENSP00000446829.3:p.Gln449=
ENST00000550345.6:c.1439A= ENSP00000450369.2:p.Gln480=
ENST00000550924.6:c.1439A= ENSP00000446945.2:p.Gln480=
ENST00000551339.6:c.1439A= ENSP00000448253.2:p.Gln480=
ENST00000642730.1:c.1748A= ENSP00000496597.1:p.Gln583=
ENST00000312352.11:c.1439A= ENSP00000309438.7:p.Gln480=
ENST00000340802.10:c.1652A= ENSP00000345771.6:p.Gln551=
ENST00000359794.9:c.1439A= ENSP00000352842.5:p.Gln480=
ENST00000546465.1:c.284A= ENSP00000446519.1:p.Gln95=
ENST00000546964.5:n.1763A=
ENST00000547581.5:c.*1707A= ENSP00000447992.1:n.*1707A=
ENST00000547587.5:c.1439A= ENSP00000449426.1:p.Gln480=
ENST00000550802.1:n.71A=
ENST00000551804.5:c.1346A= ENSP00000448177.1:p.Gln449=
ENST00000552214.1:n.95A=
ENST00000552752.5:c.588A=
ENST00000552818.1:n.62A=
NM_000289.5:c.1439A= NP_000280.1:p.Gln480=
NM_001166686.1:c.1652A= NP_001160158.1:p.Gln551=
NM_001166687.1:c.1439A= NP_001160159.1:p.Gln480=
NM_001166688.1:c.1439A= NP_001160160.1:p.Gln480=
XM_005268974.1:c.1748A= XP_005269031.1:p.Gln583=
XM_005268975.1:c.1748A= XP_005269032.1:p.Gln583=
XM_005268976.2:c.1748A= XP_005269033.1:p.Gln583=
XM_005268977.1:c.1652A= XP_005269034.1:p.Gln551=
XM_005268978.2:c.1652A= XP_005269035.1:p.Gln551=
XM_005268979.1:c.1652A= XP_005269036.1:p.Gln551=
XM_011538487.1:c.1655A= XP_011536789.1:p.Gln552=
XM_011538488.1:c.1439A= XP_011536790.1:p.Gln480=
NM_000289.6:c.1439A= MANE Select NP_000280.1:p.Gln480=
NM_001166686.2:c.1652A= NP_001160158.1:p.Gln551=
NM_001354735.1:c.1748A= NP_001341664.1:p.Gln583=
NM_001354736.1:c.1748A= NP_001341665.1:p.Gln583=
NM_001354737.1:c.1652A= NP_001341666.1:p.Gln551=
NM_001354738.1:c.1652A= NP_001341667.1:p.Gln551=
NM_001354739.1:c.1652A= NP_001341668.1:p.Gln551=
NM_001354740.1:c.1583A= NP_001341669.1:p.Gln528=
NM_001354741.1:c.1463A= NP_001341670.1:p.Gln488=
NM_001354742.1:c.1439A= NP_001341671.1:p.Gln480=
NM_001354743.1:c.1439A= NP_001341672.1:p.Gln480=
NM_001354744.1:c.1439A= NP_001341673.1:p.Gln480=
NM_001354745.1:c.1352A= NP_001341674.1:p.Gln451=
NM_001354746.1:c.1313A= NP_001341675.1:p.Gln438=
NM_001354747.1:c.1289A= NP_001341676.1:p.Gln430=
NM_001354748.1:c.1289A= NP_001341677.1:p.Gln430=
NM_001363619.1:c.1346A= NP_001350548.1:p.Gln449=
NR_148954.1:n.1876A=
NR_148955.1:n.2512A=
NR_148956.1:n.1802A=
NR_148957.1:n.2031A=
NR_148958.1:n.1779A=
NR_148959.1:n.1705A=
XM_005268976.3:c.1748A= XP_005269033.1:p.Gln583=
XM_017019469.1:c.1559A= XP_016874958.1:p.Gln520=
XM_024449020.1:c.1661A= XP_024304788.1:p.Gln554=
XM_024449021.1:c.1538A= XP_024304789.1:p.Gln513=
XM_024449022.1:c.1439A= XP_024304790.1:p.Gln480=
NM_001166687.2:c.1439A= NP_001160159.1:p.Gln480=
NM_001166688.2:c.1439A= NP_001160160.1:p.Gln480=
NM_001354741.2:c.1463A= NP_001341670.1:p.Gln488=
NM_001354742.2:c.1439A= NP_001341671.1:p.Gln480=
NM_001354743.2:c.1439A= NP_001341672.1:p.Gln480=
NM_001354744.2:c.1439A= NP_001341673.1:p.Gln480=
NM_001354745.2:c.1352A= NP_001341674.1:p.Gln451=
NM_001354746.2:c.1313A= NP_001341675.1:p.Gln438=
NM_001354747.2:c.1289A= NP_001341676.1:p.Gln430=
NM_001354748.2:c.1289A= NP_001341677.1:p.Gln430=
NM_001363619.2:c.1346A= NP_001350548.1:p.Gln449=
NR_148954.2:n.1742A=
NR_148956.2:n.1668A=
NR_148957.2:n.1897A=
NR_148958.2:n.1645A=
NR_148959.2:n.1571A=