Canonical Allele Identifier: CA384551752

Gene: PFKM

Linked Data

• MyVariant Identifiers: chr12:g.48535555G>C (hg19) ; chr12:g.48141772G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48141772G>C , CM000674.2:g.48141772G>C	GRCh38
NC_000012.11:g.48535555G>C , CM000674.1:g.48535555G>C	GRCh37
NC_000012.10:g.46821822G>C	NCBI36
NG_016199.1:g.40900G>C
NG_016199.2:g.41520G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000550257.7:c.1667G>C	ENSP00000447997.3:p.Ser556Thr
ENST00000340802.12:c.1658G>C	ENSP00000345771.6:p.Ser553Thr
ENST00000359794.11:c.1445G>C MANE Select	ENSP00000352842.5:p.Ser482Thr
ENST00000549941.7:c.1352G>C	ENSP00000446829.3:p.Ser451Thr
ENST00000550345.6:c.1445G>C	ENSP00000450369.2:p.Ser482Thr
ENST00000550924.6:c.1445G>C	ENSP00000446945.2:p.Ser482Thr
ENST00000551339.6:c.1445G>C	ENSP00000448253.2:p.Ser482Thr
ENST00000642730.1:c.1754G>C	ENSP00000496597.1:p.Ser585Thr
ENST00000312352.11:c.1445G>C	ENSP00000309438.7:p.Ser482Thr
ENST00000340802.10:c.1658G>C	ENSP00000345771.6:p.Ser553Thr
ENST00000359794.9:c.1445G>C	ENSP00000352842.5:p.Ser482Thr
ENST00000546465.1:c.290G>C	ENSP00000446519.1:p.Ser97Thr
ENST00000546964.5:n.1769G>C
ENST00000547581.5:c.*1713G>C	ENSP00000447992.1:n.*1713G>C
ENST00000547587.5:c.1445G>C	ENSP00000449426.1:p.Ser482Thr
ENST00000550802.1:n.77G>C
ENST00000551804.5:c.1352G>C	ENSP00000448177.1:p.Ser451Thr
ENST00000552214.1:n.101G>C
ENST00000552752.5:c.594G>C
ENST00000552818.1:n.68G>C
NM_000289.5:c.1445G>C	NP_000280.1:p.Ser482Thr
NM_001166686.1:c.1658G>C	NP_001160158.1:p.Ser553Thr
NM_001166687.1:c.1445G>C	NP_001160159.1:p.Ser482Thr
NM_001166688.1:c.1445G>C	NP_001160160.1:p.Ser482Thr
XM_005268974.1:c.1754G>C	XP_005269031.1:p.Ser585Thr
XM_005268975.1:c.1754G>C	XP_005269032.1:p.Ser585Thr
XM_005268976.2:c.1754G>C	XP_005269033.1:p.Ser585Thr
XM_005268977.1:c.1658G>C	XP_005269034.1:p.Ser553Thr
XM_005268978.2:c.1658G>C	XP_005269035.1:p.Ser553Thr
XM_005268979.1:c.1658G>C	XP_005269036.1:p.Ser553Thr
XM_011538487.1:c.1661G>C	XP_011536789.1:p.Ser554Thr
XM_011538488.1:c.1445G>C	XP_011536790.1:p.Ser482Thr
NM_000289.6:c.1445G>C MANE Select	NP_000280.1:p.Ser482Thr
NM_001166686.2:c.1658G>C	NP_001160158.1:p.Ser553Thr
NM_001354735.1:c.1754G>C	NP_001341664.1:p.Ser585Thr
NM_001354736.1:c.1754G>C	NP_001341665.1:p.Ser585Thr
NM_001354737.1:c.1658G>C	NP_001341666.1:p.Ser553Thr
NM_001354738.1:c.1658G>C	NP_001341667.1:p.Ser553Thr
NM_001354739.1:c.1658G>C	NP_001341668.1:p.Ser553Thr
NM_001354740.1:c.1589G>C	NP_001341669.1:p.Ser530Thr
NM_001354741.1:c.1469G>C	NP_001341670.1:p.Ser490Thr
NM_001354742.1:c.1445G>C	NP_001341671.1:p.Ser482Thr
NM_001354743.1:c.1445G>C	NP_001341672.1:p.Ser482Thr
NM_001354744.1:c.1445G>C	NP_001341673.1:p.Ser482Thr
NM_001354745.1:c.1358G>C	NP_001341674.1:p.Ser453Thr
NM_001354746.1:c.1319G>C	NP_001341675.1:p.Ser440Thr
NM_001354747.1:c.1295G>C	NP_001341676.1:p.Ser432Thr
NM_001354748.1:c.1295G>C	NP_001341677.1:p.Ser432Thr
NM_001363619.1:c.1352G>C	NP_001350548.1:p.Ser451Thr
NR_148954.1:n.1882G>C
NR_148955.1:n.2518G>C
NR_148956.1:n.1808G>C
NR_148957.1:n.2037G>C
NR_148958.1:n.1785G>C
NR_148959.1:n.1711G>C
XM_005268976.3:c.1754G>C	XP_005269033.1:p.Ser585Thr
XM_017019469.1:c.1565G>C	XP_016874958.1:p.Ser522Thr
XM_024449020.1:c.1667G>C	XP_024304788.1:p.Ser556Thr
XM_024449021.1:c.1544G>C	XP_024304789.1:p.Ser515Thr
XM_024449022.1:c.1445G>C	XP_024304790.1:p.Ser482Thr
NM_001166687.2:c.1445G>C	NP_001160159.1:p.Ser482Thr
NM_001166688.2:c.1445G>C	NP_001160160.1:p.Ser482Thr
NM_001354741.2:c.1469G>C	NP_001341670.1:p.Ser490Thr
NM_001354742.2:c.1445G>C	NP_001341671.1:p.Ser482Thr
NM_001354743.2:c.1445G>C	NP_001341672.1:p.Ser482Thr
NM_001354744.2:c.1445G>C	NP_001341673.1:p.Ser482Thr
NM_001354745.2:c.1358G>C	NP_001341674.1:p.Ser453Thr
NM_001354746.2:c.1319G>C	NP_001341675.1:p.Ser440Thr
NM_001354747.2:c.1295G>C	NP_001341676.1:p.Ser432Thr
NM_001354748.2:c.1295G>C	NP_001341677.1:p.Ser432Thr
NM_001363619.2:c.1352G>C	NP_001350548.1:p.Ser451Thr
NR_148954.2:n.1748G>C
NR_148956.2:n.1674G>C
NR_148957.2:n.1903G>C
NR_148958.2:n.1651G>C
NR_148959.2:n.1577G>C