Canonical Allele Identifier: CA384555810

Gene: PFKM

Linked Data

• MyVariant Identifiers: chr12:g.48538857T>G (hg19) ; chr12:g.48145074T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48145074T>G , CM000674.2:g.48145074T>G	GRCh38
NC_000012.11:g.48538857T>G , CM000674.1:g.48538857T>G	GRCh37
NC_000012.10:g.46825124T>G	NCBI36
NG_016199.1:g.44202T>G
NG_016199.2:g.44822T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000550257.7:c.2258T>G	ENSP00000447997.3:p.Met753Arg
ENST00000340802.12:c.2249T>G	ENSP00000345771.6:p.Met750Arg
ENST00000359794.11:c.2036T>G MANE Select	ENSP00000352842.5:p.Met679Arg
ENST00000549941.7:c.1778T>G	ENSP00000446829.3:p.Met593Arg
ENST00000550345.6:c.2036T>G	ENSP00000450369.2:p.Met679Arg
ENST00000550924.6:c.2036T>G	ENSP00000446945.2:p.Met679Arg
ENST00000551339.6:c.2036T>G	ENSP00000448253.2:p.Met679Arg
ENST00000642730.1:c.2345T>G	ENSP00000496597.1:p.Met782Arg
ENST00000312352.11:c.2036T>G	ENSP00000309438.7:p.Met679Arg
ENST00000340802.10:c.2249T>G	ENSP00000345771.6:p.Met750Arg
ENST00000359794.9:c.2036T>G	ENSP00000352842.5:p.Met679Arg
ENST00000546964.5:n.2360T>G
ENST00000547581.5:c.*2304T>G	ENSP00000447992.1:n.*2304T>G
ENST00000547587.5:c.2036T>G	ENSP00000449426.1:p.Met679Arg
ENST00000551804.5:c.1943T>G	ENSP00000448177.1:p.Met648Arg
NM_000289.5:c.2036T>G	NP_000280.1:p.Met679Arg
NM_001166686.1:c.2249T>G	NP_001160158.1:p.Met750Arg
NM_001166687.1:c.2036T>G	NP_001160159.1:p.Met679Arg
NM_001166688.1:c.2036T>G	NP_001160160.1:p.Met679Arg
XM_005268974.1:c.2345T>G	XP_005269031.1:p.Met782Arg
XM_005268975.1:c.2345T>G	XP_005269032.1:p.Met782Arg
XM_005268976.2:c.2345T>G	XP_005269033.1:p.Met782Arg
XM_005268977.1:c.2249T>G	XP_005269034.1:p.Met750Arg
XM_005268978.2:c.2249T>G	XP_005269035.1:p.Met750Arg
XM_005268979.1:c.2249T>G	XP_005269036.1:p.Met750Arg
XM_011538487.1:c.2252T>G	XP_011536789.1:p.Met751Arg
XM_011538488.1:c.2036T>G	XP_011536790.1:p.Met679Arg
NM_000289.6:c.2036T>G MANE Select	NP_000280.1:p.Met679Arg
NM_001166686.2:c.2249T>G	NP_001160158.1:p.Met750Arg
NM_001354735.1:c.2345T>G	NP_001341664.1:p.Met782Arg
NM_001354736.1:c.2345T>G	NP_001341665.1:p.Met782Arg
NM_001354737.1:c.2249T>G	NP_001341666.1:p.Met750Arg
NM_001354738.1:c.2249T>G	NP_001341667.1:p.Met750Arg
NM_001354739.1:c.2249T>G	NP_001341668.1:p.Met750Arg
NM_001354740.1:c.2180T>G	NP_001341669.1:p.Met727Arg
NM_001354741.1:c.2060T>G	NP_001341670.1:p.Met687Arg
NM_001354742.1:c.2036T>G	NP_001341671.1:p.Met679Arg
NM_001354743.1:c.2036T>G	NP_001341672.1:p.Met679Arg
NM_001354744.1:c.2036T>G	NP_001341673.1:p.Met679Arg
NM_001354745.1:c.1949T>G	NP_001341674.1:p.Met650Arg
NM_001354746.1:c.1910T>G	NP_001341675.1:p.Met637Arg
NM_001354747.1:c.1886T>G	NP_001341676.1:p.Met629Arg
NM_001354748.1:c.1886T>G	NP_001341677.1:p.Met629Arg
NM_001363619.1:c.1943T>G	NP_001350548.1:p.Met648Arg
NR_148954.1:n.2473T>G
NR_148955.1:n.3109T>G
NR_148956.1:n.2399T>G
NR_148957.1:n.2628T>G
NR_148958.1:n.2376T>G
NR_148959.1:n.2302T>G
XM_005268976.3:c.2345T>G	XP_005269033.1:p.Met782Arg
XM_017019469.1:c.2156T>G	XP_016874958.1:p.Met719Arg
XM_024449020.1:c.2258T>G	XP_024304788.1:p.Met753Arg
XM_024449021.1:c.2135T>G	XP_024304789.1:p.Met712Arg
XM_024449022.1:c.2036T>G	XP_024304790.1:p.Met679Arg
NM_001166687.2:c.2036T>G	NP_001160159.1:p.Met679Arg
NM_001166688.2:c.2036T>G	NP_001160160.1:p.Met679Arg
NM_001354741.2:c.2060T>G	NP_001341670.1:p.Met687Arg
NM_001354742.2:c.2036T>G	NP_001341671.1:p.Met679Arg
NM_001354743.2:c.2036T>G	NP_001341672.1:p.Met679Arg
NM_001354744.2:c.2036T>G	NP_001341673.1:p.Met679Arg
NM_001354745.2:c.1949T>G	NP_001341674.1:p.Met650Arg
NM_001354746.2:c.1910T>G	NP_001341675.1:p.Met637Arg
NM_001354747.2:c.1886T>G	NP_001341676.1:p.Met629Arg
NM_001354748.2:c.1886T>G	NP_001341677.1:p.Met629Arg
NM_001363619.2:c.1943T>G	NP_001350548.1:p.Met648Arg
NR_148954.2:n.2339T>G
NR_148956.2:n.2265T>G
NR_148957.2:n.2494T>G
NR_148958.2:n.2242T>G
NR_148959.2:n.2168T>G