Canonical Allele Identifier: CA384551927

Gene: PFKM

Linked Data

• MyVariant Identifiers: chr12:g.48535578A>C (hg19) ; chr12:g.48141795A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48141795A>C , CM000674.2:g.48141795A>C	GRCh38
NC_000012.11:g.48535578A>C , CM000674.1:g.48535578A>C	GRCh37
NC_000012.10:g.46821845A>C	NCBI36
NG_016199.1:g.40923A>C
NG_016199.2:g.41543A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000550257.7:c.1690A>C	ENSP00000447997.3:p.Ile564Leu
ENST00000340802.12:c.1681A>C	ENSP00000345771.6:p.Ile561Leu
ENST00000359794.11:c.1468A>C MANE Select	ENSP00000352842.5:p.Ile490Leu
ENST00000549941.7:c.1375A>C	ENSP00000446829.3:p.Ile459Leu
ENST00000550345.6:c.1468A>C	ENSP00000450369.2:p.Ile490Leu
ENST00000550924.6:c.1468A>C	ENSP00000446945.2:p.Ile490Leu
ENST00000551339.6:c.1468A>C	ENSP00000448253.2:p.Ile490Leu
ENST00000642730.1:c.1777A>C	ENSP00000496597.1:p.Ile593Leu
ENST00000312352.11:c.1468A>C	ENSP00000309438.7:p.Ile490Leu
ENST00000340802.10:c.1681A>C	ENSP00000345771.6:p.Ile561Leu
ENST00000359794.9:c.1468A>C	ENSP00000352842.5:p.Ile490Leu
ENST00000546465.1:c.313A>C	ENSP00000446519.1:p.Ile105Leu
ENST00000546964.5:n.1792A>C
ENST00000547581.5:c.*1736A>C	ENSP00000447992.1:n.*1736A>C
ENST00000547587.5:c.1468A>C	ENSP00000449426.1:p.Ile490Leu
ENST00000550802.1:n.100A>C
ENST00000551804.5:c.1375A>C	ENSP00000448177.1:p.Ile459Leu
ENST00000552214.1:n.124A>C
ENST00000552752.5:c.617A>C
ENST00000552818.1:n.91A>C
NM_000289.5:c.1468A>C	NP_000280.1:p.Ile490Leu
NM_001166686.1:c.1681A>C	NP_001160158.1:p.Ile561Leu
NM_001166687.1:c.1468A>C	NP_001160159.1:p.Ile490Leu
NM_001166688.1:c.1468A>C	NP_001160160.1:p.Ile490Leu
XM_005268974.1:c.1777A>C	XP_005269031.1:p.Ile593Leu
XM_005268975.1:c.1777A>C	XP_005269032.1:p.Ile593Leu
XM_005268976.2:c.1777A>C	XP_005269033.1:p.Ile593Leu
XM_005268977.1:c.1681A>C	XP_005269034.1:p.Ile561Leu
XM_005268978.2:c.1681A>C	XP_005269035.1:p.Ile561Leu
XM_005268979.1:c.1681A>C	XP_005269036.1:p.Ile561Leu
XM_011538487.1:c.1684A>C	XP_011536789.1:p.Ile562Leu
XM_011538488.1:c.1468A>C	XP_011536790.1:p.Ile490Leu
NM_000289.6:c.1468A>C MANE Select	NP_000280.1:p.Ile490Leu
NM_001166686.2:c.1681A>C	NP_001160158.1:p.Ile561Leu
NM_001354735.1:c.1777A>C	NP_001341664.1:p.Ile593Leu
NM_001354736.1:c.1777A>C	NP_001341665.1:p.Ile593Leu
NM_001354737.1:c.1681A>C	NP_001341666.1:p.Ile561Leu
NM_001354738.1:c.1681A>C	NP_001341667.1:p.Ile561Leu
NM_001354739.1:c.1681A>C	NP_001341668.1:p.Ile561Leu
NM_001354740.1:c.1612A>C	NP_001341669.1:p.Ile538Leu
NM_001354741.1:c.1492A>C	NP_001341670.1:p.Ile498Leu
NM_001354742.1:c.1468A>C	NP_001341671.1:p.Ile490Leu
NM_001354743.1:c.1468A>C	NP_001341672.1:p.Ile490Leu
NM_001354744.1:c.1468A>C	NP_001341673.1:p.Ile490Leu
NM_001354745.1:c.1381A>C	NP_001341674.1:p.Ile461Leu
NM_001354746.1:c.1342A>C	NP_001341675.1:p.Ile448Leu
NM_001354747.1:c.1318A>C	NP_001341676.1:p.Ile440Leu
NM_001354748.1:c.1318A>C	NP_001341677.1:p.Ile440Leu
NM_001363619.1:c.1375A>C	NP_001350548.1:p.Ile459Leu
NR_148954.1:n.1905A>C
NR_148955.1:n.2541A>C
NR_148956.1:n.1831A>C
NR_148957.1:n.2060A>C
NR_148958.1:n.1808A>C
NR_148959.1:n.1734A>C
XM_005268976.3:c.1777A>C	XP_005269033.1:p.Ile593Leu
XM_017019469.1:c.1588A>C	XP_016874958.1:p.Ile530Leu
XM_024449020.1:c.1690A>C	XP_024304788.1:p.Ile564Leu
XM_024449021.1:c.1567A>C	XP_024304789.1:p.Ile523Leu
XM_024449022.1:c.1468A>C	XP_024304790.1:p.Ile490Leu
NM_001166687.2:c.1468A>C	NP_001160159.1:p.Ile490Leu
NM_001166688.2:c.1468A>C	NP_001160160.1:p.Ile490Leu
NM_001354741.2:c.1492A>C	NP_001341670.1:p.Ile498Leu
NM_001354742.2:c.1468A>C	NP_001341671.1:p.Ile490Leu
NM_001354743.2:c.1468A>C	NP_001341672.1:p.Ile490Leu
NM_001354744.2:c.1468A>C	NP_001341673.1:p.Ile490Leu
NM_001354745.2:c.1381A>C	NP_001341674.1:p.Ile461Leu
NM_001354746.2:c.1342A>C	NP_001341675.1:p.Ile448Leu
NM_001354747.2:c.1318A>C	NP_001341676.1:p.Ile440Leu
NM_001354748.2:c.1318A>C	NP_001341677.1:p.Ile440Leu
NM_001363619.2:c.1375A>C	NP_001350548.1:p.Ile459Leu
NR_148954.2:n.1771A>C
NR_148956.2:n.1697A>C
NR_148957.2:n.1926A>C
NR_148958.2:n.1674A>C
NR_148959.2:n.1600A>C