Canonical Allele Identifier: CA479459897

Gene: PFKM

Linked Data

• MyVariant Identifiers: chr12:g.48538909T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48145126T>C , CM000674.2:g.48145126T>C	GRCh38
NC_000012.11:g.48538909T>C , CM000674.1:g.48538909T>C	GRCh37
NC_000012.10:g.46825176T>C	NCBI36
NG_016199.1:g.44254T>C
NG_016199.2:g.44874T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000550257.7:c.2310T>C	ENSP00000447997.3:p.Arg770=
ENST00000340802.12:c.2301T>C	ENSP00000345771.6:p.Arg767=
ENST00000359794.11:c.2088T>C MANE Select	ENSP00000352842.5:p.Arg696=
ENST00000549941.7:c.1830T>C	ENSP00000446829.3:p.Arg610=
ENST00000550345.6:c.2088T>C	ENSP00000450369.2:p.Arg696=
ENST00000550924.6:c.2088T>C	ENSP00000446945.2:p.Arg696=
ENST00000551339.6:c.2088T>C	ENSP00000448253.2:p.Arg696=
ENST00000642730.1:c.2397T>C	ENSP00000496597.1:p.Arg799=
ENST00000312352.11:c.2088T>C	ENSP00000309438.7:p.Arg696=
ENST00000340802.10:c.2301T>C	ENSP00000345771.6:p.Arg767=
ENST00000359794.9:c.2088T>C	ENSP00000352842.5:p.Arg696=
ENST00000546964.5:n.2412T>C
ENST00000547581.5:c.*2356T>C	ENSP00000447992.1:n.*2356T>C
ENST00000547587.5:c.2088T>C	ENSP00000449426.1:p.Arg696=
ENST00000551804.5:c.1995T>C	ENSP00000448177.1:p.Arg665=
NM_000289.5:c.2088T>C	NP_000280.1:p.Arg696=
NM_001166686.1:c.2301T>C	NP_001160158.1:p.Arg767=
NM_001166687.1:c.2088T>C	NP_001160159.1:p.Arg696=
NM_001166688.1:c.2088T>C	NP_001160160.1:p.Arg696=
XM_005268974.1:c.2397T>C	XP_005269031.1:p.Arg799=
XM_005268975.1:c.2397T>C	XP_005269032.1:p.Arg799=
XM_005268976.2:c.2397T>C	XP_005269033.1:p.Arg799=
XM_005268977.1:c.2301T>C	XP_005269034.1:p.Arg767=
XM_005268978.2:c.2301T>C	XP_005269035.1:p.Arg767=
XM_005268979.1:c.2301T>C	XP_005269036.1:p.Arg767=
XM_011538487.1:c.2304T>C	XP_011536789.1:p.Arg768=
XM_011538488.1:c.2088T>C	XP_011536790.1:p.Arg696=
NM_000289.6:c.2088T>C MANE Select	NP_000280.1:p.Arg696=
NM_001166686.2:c.2301T>C	NP_001160158.1:p.Arg767=
NM_001354735.1:c.2397T>C	NP_001341664.1:p.Arg799=
NM_001354736.1:c.2397T>C	NP_001341665.1:p.Arg799=
NM_001354737.1:c.2301T>C	NP_001341666.1:p.Arg767=
NM_001354738.1:c.2301T>C	NP_001341667.1:p.Arg767=
NM_001354739.1:c.2301T>C	NP_001341668.1:p.Arg767=
NM_001354740.1:c.2232T>C	NP_001341669.1:p.Arg744=
NM_001354741.1:c.2112T>C	NP_001341670.1:p.Arg704=
NM_001354742.1:c.2088T>C	NP_001341671.1:p.Arg696=
NM_001354743.1:c.2088T>C	NP_001341672.1:p.Arg696=
NM_001354744.1:c.2088T>C	NP_001341673.1:p.Arg696=
NM_001354745.1:c.2001T>C	NP_001341674.1:p.Arg667=
NM_001354746.1:c.1962T>C	NP_001341675.1:p.Arg654=
NM_001354747.1:c.1938T>C	NP_001341676.1:p.Arg646=
NM_001354748.1:c.1938T>C	NP_001341677.1:p.Arg646=
NM_001363619.1:c.1995T>C	NP_001350548.1:p.Arg665=
NR_148954.1:n.2525T>C
NR_148955.1:n.3161T>C
NR_148956.1:n.2451T>C
NR_148957.1:n.2680T>C
NR_148958.1:n.2428T>C
NR_148959.1:n.2354T>C
XM_005268976.3:c.2397T>C	XP_005269033.1:p.Arg799=
XM_017019469.1:c.2208T>C	XP_016874958.1:p.Arg736=
XM_024449020.1:c.2310T>C	XP_024304788.1:p.Arg770=
XM_024449021.1:c.2187T>C	XP_024304789.1:p.Arg729=
XM_024449022.1:c.2088T>C	XP_024304790.1:p.Arg696=
NM_001166687.2:c.2088T>C	NP_001160159.1:p.Arg696=
NM_001166688.2:c.2088T>C	NP_001160160.1:p.Arg696=
NM_001354741.2:c.2112T>C	NP_001341670.1:p.Arg704=
NM_001354742.2:c.2088T>C	NP_001341671.1:p.Arg696=
NM_001354743.2:c.2088T>C	NP_001341672.1:p.Arg696=
NM_001354744.2:c.2088T>C	NP_001341673.1:p.Arg696=
NM_001354745.2:c.2001T>C	NP_001341674.1:p.Arg667=
NM_001354746.2:c.1962T>C	NP_001341675.1:p.Arg654=
NM_001354747.2:c.1938T>C	NP_001341676.1:p.Arg646=
NM_001354748.2:c.1938T>C	NP_001341677.1:p.Arg646=
NM_001363619.2:c.1995T>C	NP_001350548.1:p.Arg665=
NR_148954.2:n.2391T>C
NR_148956.2:n.2317T>C
NR_148957.2:n.2546T>C
NR_148958.2:n.2294T>C
NR_148959.2:n.2220T>C