Canonical Allele Identifier: CA2034529163

Gene: PFKM

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48132875C= , CM000674.2:g.48132875C=	GRCh38
NC_000012.11:g.48526658C= , CM000674.1:g.48526658C=	GRCh37
NC_000012.10:g.46812925C=	NCBI36
NG_016199.1:g.32003C=
NG_016199.2:g.32623C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000550257.7:c.467C=	ENSP00000447997.3:p.Thr156=
ENST00000340802.12:c.458C=	ENSP00000345771.6:p.Thr153=
ENST00000359794.11:c.245C= MANE Select	ENSP00000352842.5:p.Thr82=
ENST00000549941.7:c.245C=	ENSP00000446829.3:p.Thr82=
ENST00000550345.6:c.245C=	ENSP00000450369.2:p.Thr82=
ENST00000550924.6:c.245C=	ENSP00000446945.2:p.Thr82=
ENST00000551339.6:c.245C=	ENSP00000448253.2:p.Thr82=
ENST00000642730.1:c.554C=	ENSP00000496597.1:p.Thr185=
ENST00000312352.11:c.245C=	ENSP00000309438.7:p.Thr82=
ENST00000340802.10:c.458C=	ENSP00000345771.6:p.Thr153=
ENST00000359794.9:c.245C=	ENSP00000352842.5:p.Thr82=
ENST00000546465.1:c.86-7896C=	ENSP00000446519.1:n.86-7896C=
ENST00000546964.5:n.317C=
ENST00000547581.5:c.*261C=	ENSP00000447992.1:n.*261C=
ENST00000547587.5:c.245C=	ENSP00000449426.1:p.Thr82=
ENST00000548345.5:c.245C=	ENSP00000449269.1:p.Thr82=
ENST00000549003.5:c.245C=	ENSP00000449835.1:p.Thr82=
ENST00000549022.5:c.245C=	ENSP00000446805.1:p.Thr82=
ENST00000549941.5:c.344C=	ENSP00000446829.1:p.Thr115=
ENST00000550345.5:c.245C=	ENSP00000450369.1:p.Thr82=
ENST00000550924.5:c.245C=	ENSP00000446945.1:p.Thr82=
ENST00000551339.5:c.245C=	ENSP00000448253.1:p.Thr82=
ENST00000551485.5:c.*129C=	ENSP00000448315.1:n.*129C=
ENST00000551804.5:c.245C=	ENSP00000448177.1:p.Thr82=
ENST00000552989.5:c.86-1364C=	ENSP00000447774.1:n.86-1364C=
NM_000289.5:c.245C=	NP_000280.1:p.Thr82=
NM_001166686.1:c.458C=	NP_001160158.1:p.Thr153=
NM_001166687.1:c.245C=	NP_001160159.1:p.Thr82=
NM_001166688.1:c.245C=	NP_001160160.1:p.Thr82=
XM_005268974.1:c.554C=	XP_005269031.1:p.Thr185=
XM_005268975.1:c.554C=	XP_005269032.1:p.Thr185=
XM_005268976.2:c.554C=	XP_005269033.1:p.Thr185=
XM_005268977.1:c.458C=	XP_005269034.1:p.Thr153=
XM_005268978.2:c.458C=	XP_005269035.1:p.Thr153=
XM_005268979.1:c.458C=	XP_005269036.1:p.Thr153=
XM_011538487.1:c.554C=	XP_011536789.1:p.Thr185=
XM_011538488.1:c.245C=	XP_011536790.1:p.Thr82=
NM_000289.6:c.245C= MANE Select	NP_000280.1:p.Thr82=
NM_001166686.2:c.458C=	NP_001160158.1:p.Thr153=
NM_001354735.1:c.554C=	NP_001341664.1:p.Thr185=
NM_001354736.1:c.554C=	NP_001341665.1:p.Thr185=
NM_001354737.1:c.458C=	NP_001341666.1:p.Thr153=
NM_001354738.1:c.458C=	NP_001341667.1:p.Thr153=
NM_001354739.1:c.458C=	NP_001341668.1:p.Thr153=
NM_001354740.1:c.389C=	NP_001341669.1:p.Thr130=
NM_001354741.1:c.269C=	NP_001341670.1:p.Thr90=
NM_001354742.1:c.245C=	NP_001341671.1:p.Thr82=
NM_001354743.1:c.245C=	NP_001341672.1:p.Thr82=
NM_001354744.1:c.245C=	NP_001341673.1:p.Thr82=
NM_001354745.1:c.158C=	NP_001341674.1:p.Thr53=
NM_001354746.1:c.245C=	NP_001341675.1:p.Thr82=
NM_001354747.1:c.95C=	NP_001341676.1:p.Thr32=
NM_001354748.1:c.95C=	NP_001341677.1:p.Thr32=
NM_001363619.1:c.245C=	NP_001350548.1:p.Thr82=
NR_148954.1:n.430C=
NR_148955.1:n.1066C=
NR_148956.1:n.356C=
NR_148957.1:n.430C=
NR_148958.1:n.430C=
NR_148959.1:n.356C=
XM_005268976.3:c.554C=	XP_005269033.1:p.Thr185=
XM_017019469.1:c.458C=	XP_016874958.1:p.Thr153=
XM_024449020.1:c.467C=	XP_024304788.1:p.Thr156=
XM_024449021.1:c.344C=	XP_024304789.1:p.Thr115=
XM_024449022.1:c.245C=	XP_024304790.1:p.Thr82=
NM_001166687.2:c.245C=	NP_001160159.1:p.Thr82=
NM_001166688.2:c.245C=	NP_001160160.1:p.Thr82=
NM_001354741.2:c.269C=	NP_001341670.1:p.Thr90=
NM_001354742.2:c.245C=	NP_001341671.1:p.Thr82=
NM_001354743.2:c.245C=	NP_001341672.1:p.Thr82=
NM_001354744.2:c.245C=	NP_001341673.1:p.Thr82=
NM_001354745.2:c.158C=	NP_001341674.1:p.Thr53=
NM_001354746.2:c.245C=	NP_001341675.1:p.Thr82=
NM_001354747.2:c.95C=	NP_001341676.1:p.Thr32=
NM_001354748.2:c.95C=	NP_001341677.1:p.Thr32=
NM_001363619.2:c.245C=	NP_001350548.1:p.Thr82=
NR_148954.2:n.296C=
NR_148956.2:n.222C=
NR_148957.2:n.296C=
NR_148958.2:n.296C=
NR_148959.2:n.222C=