Canonical Allele Identifier: CA479459758
Gene: PFKM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48145087T>G , CM000674.2:g.48145087T>G GRCh38
NC_000012.11:g.48538870T>G , CM000674.1:g.48538870T>G GRCh37
NC_000012.10:g.46825137T>G NCBI36
NG_016199.1:g.44215T>G
NG_016199.2:g.44835T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000550257.7:c.2271T>G ENSP00000447997.3:p.Ala757=
ENST00000340802.12:c.2262T>G ENSP00000345771.6:p.Ala754=
ENST00000359794.11:c.2049T>G MANE Select ENSP00000352842.5:p.Ala683=
ENST00000549941.7:c.1791T>G ENSP00000446829.3:p.Ala597=
ENST00000550345.6:c.2049T>G ENSP00000450369.2:p.Ala683=
ENST00000550924.6:c.2049T>G ENSP00000446945.2:p.Ala683=
ENST00000551339.6:c.2049T>G ENSP00000448253.2:p.Ala683=
ENST00000642730.1:c.2358T>G ENSP00000496597.1:p.Ala786=
ENST00000312352.11:c.2049T>G ENSP00000309438.7:p.Ala683=
ENST00000340802.10:c.2262T>G ENSP00000345771.6:p.Ala754=
ENST00000359794.9:c.2049T>G ENSP00000352842.5:p.Ala683=
ENST00000546964.5:n.2373T>G
ENST00000547581.5:c.*2317T>G ENSP00000447992.1:n.*2317T>G
ENST00000547587.5:c.2049T>G ENSP00000449426.1:p.Ala683=
ENST00000551804.5:c.1956T>G ENSP00000448177.1:p.Ala652=
NM_000289.5:c.2049T>G NP_000280.1:p.Ala683=
NM_001166686.1:c.2262T>G NP_001160158.1:p.Ala754=
NM_001166687.1:c.2049T>G NP_001160159.1:p.Ala683=
NM_001166688.1:c.2049T>G NP_001160160.1:p.Ala683=
XM_005268974.1:c.2358T>G XP_005269031.1:p.Ala786=
XM_005268975.1:c.2358T>G XP_005269032.1:p.Ala786=
XM_005268976.2:c.2358T>G XP_005269033.1:p.Ala786=
XM_005268977.1:c.2262T>G XP_005269034.1:p.Ala754=
XM_005268978.2:c.2262T>G XP_005269035.1:p.Ala754=
XM_005268979.1:c.2262T>G XP_005269036.1:p.Ala754=
XM_011538487.1:c.2265T>G XP_011536789.1:p.Ala755=
XM_011538488.1:c.2049T>G XP_011536790.1:p.Ala683=
NM_000289.6:c.2049T>G MANE Select NP_000280.1:p.Ala683=
NM_001166686.2:c.2262T>G NP_001160158.1:p.Ala754=
NM_001354735.1:c.2358T>G NP_001341664.1:p.Ala786=
NM_001354736.1:c.2358T>G NP_001341665.1:p.Ala786=
NM_001354737.1:c.2262T>G NP_001341666.1:p.Ala754=
NM_001354738.1:c.2262T>G NP_001341667.1:p.Ala754=
NM_001354739.1:c.2262T>G NP_001341668.1:p.Ala754=
NM_001354740.1:c.2193T>G NP_001341669.1:p.Ala731=
NM_001354741.1:c.2073T>G NP_001341670.1:p.Ala691=
NM_001354742.1:c.2049T>G NP_001341671.1:p.Ala683=
NM_001354743.1:c.2049T>G NP_001341672.1:p.Ala683=
NM_001354744.1:c.2049T>G NP_001341673.1:p.Ala683=
NM_001354745.1:c.1962T>G NP_001341674.1:p.Ala654=
NM_001354746.1:c.1923T>G NP_001341675.1:p.Ala641=
NM_001354747.1:c.1899T>G NP_001341676.1:p.Ala633=
NM_001354748.1:c.1899T>G NP_001341677.1:p.Ala633=
NM_001363619.1:c.1956T>G NP_001350548.1:p.Ala652=
NR_148954.1:n.2486T>G
NR_148955.1:n.3122T>G
NR_148956.1:n.2412T>G
NR_148957.1:n.2641T>G
NR_148958.1:n.2389T>G
NR_148959.1:n.2315T>G
XM_005268976.3:c.2358T>G XP_005269033.1:p.Ala786=
XM_017019469.1:c.2169T>G XP_016874958.1:p.Ala723=
XM_024449020.1:c.2271T>G XP_024304788.1:p.Ala757=
XM_024449021.1:c.2148T>G XP_024304789.1:p.Ala716=
XM_024449022.1:c.2049T>G XP_024304790.1:p.Ala683=
NM_001166687.2:c.2049T>G NP_001160159.1:p.Ala683=
NM_001166688.2:c.2049T>G NP_001160160.1:p.Ala683=
NM_001354741.2:c.2073T>G NP_001341670.1:p.Ala691=
NM_001354742.2:c.2049T>G NP_001341671.1:p.Ala683=
NM_001354743.2:c.2049T>G NP_001341672.1:p.Ala683=
NM_001354744.2:c.2049T>G NP_001341673.1:p.Ala683=
NM_001354745.2:c.1962T>G NP_001341674.1:p.Ala654=
NM_001354746.2:c.1923T>G NP_001341675.1:p.Ala641=
NM_001354747.2:c.1899T>G NP_001341676.1:p.Ala633=
NM_001354748.2:c.1899T>G NP_001341677.1:p.Ala633=
NM_001363619.2:c.1956T>G NP_001350548.1:p.Ala652=
NR_148954.2:n.2352T>G
NR_148956.2:n.2278T>G
NR_148957.2:n.2507T>G
NR_148958.2:n.2255T>G
NR_148959.2:n.2181T>G