Canonical Allele Identifier: CA384551787

Gene: PFKM

Linked Data

• MyVariant Identifiers: chr12:g.48535558C>G (hg19) ; chr12:g.48141775C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48141775C>G , CM000674.2:g.48141775C>G	GRCh38
NC_000012.11:g.48535558C>G , CM000674.1:g.48535558C>G	GRCh37
NC_000012.10:g.46821825C>G	NCBI36
NG_016199.1:g.40903C>G
NG_016199.2:g.41523C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000550257.7:c.1670C>G	ENSP00000447997.3:p.Ala557Gly
ENST00000340802.12:c.1661C>G	ENSP00000345771.6:p.Ala554Gly
ENST00000359794.11:c.1448C>G MANE Select	ENSP00000352842.5:p.Ala483Gly
ENST00000549941.7:c.1355C>G	ENSP00000446829.3:p.Ala452Gly
ENST00000550345.6:c.1448C>G	ENSP00000450369.2:p.Ala483Gly
ENST00000550924.6:c.1448C>G	ENSP00000446945.2:p.Ala483Gly
ENST00000551339.6:c.1448C>G	ENSP00000448253.2:p.Ala483Gly
ENST00000642730.1:c.1757C>G	ENSP00000496597.1:p.Ala586Gly
ENST00000312352.11:c.1448C>G	ENSP00000309438.7:p.Ala483Gly
ENST00000340802.10:c.1661C>G	ENSP00000345771.6:p.Ala554Gly
ENST00000359794.9:c.1448C>G	ENSP00000352842.5:p.Ala483Gly
ENST00000546465.1:c.293C>G	ENSP00000446519.1:p.Ala98Gly
ENST00000546964.5:n.1772C>G
ENST00000547581.5:c.*1716C>G	ENSP00000447992.1:n.*1716C>G
ENST00000547587.5:c.1448C>G	ENSP00000449426.1:p.Ala483Gly
ENST00000550802.1:n.80C>G
ENST00000551804.5:c.1355C>G	ENSP00000448177.1:p.Ala452Gly
ENST00000552214.1:n.104C>G
ENST00000552752.5:c.597C>G
ENST00000552818.1:n.71C>G
NM_000289.5:c.1448C>G	NP_000280.1:p.Ala483Gly
NM_001166686.1:c.1661C>G	NP_001160158.1:p.Ala554Gly
NM_001166687.1:c.1448C>G	NP_001160159.1:p.Ala483Gly
NM_001166688.1:c.1448C>G	NP_001160160.1:p.Ala483Gly
XM_005268974.1:c.1757C>G	XP_005269031.1:p.Ala586Gly
XM_005268975.1:c.1757C>G	XP_005269032.1:p.Ala586Gly
XM_005268976.2:c.1757C>G	XP_005269033.1:p.Ala586Gly
XM_005268977.1:c.1661C>G	XP_005269034.1:p.Ala554Gly
XM_005268978.2:c.1661C>G	XP_005269035.1:p.Ala554Gly
XM_005268979.1:c.1661C>G	XP_005269036.1:p.Ala554Gly
XM_011538487.1:c.1664C>G	XP_011536789.1:p.Ala555Gly
XM_011538488.1:c.1448C>G	XP_011536790.1:p.Ala483Gly
NM_000289.6:c.1448C>G MANE Select	NP_000280.1:p.Ala483Gly
NM_001166686.2:c.1661C>G	NP_001160158.1:p.Ala554Gly
NM_001354735.1:c.1757C>G	NP_001341664.1:p.Ala586Gly
NM_001354736.1:c.1757C>G	NP_001341665.1:p.Ala586Gly
NM_001354737.1:c.1661C>G	NP_001341666.1:p.Ala554Gly
NM_001354738.1:c.1661C>G	NP_001341667.1:p.Ala554Gly
NM_001354739.1:c.1661C>G	NP_001341668.1:p.Ala554Gly
NM_001354740.1:c.1592C>G	NP_001341669.1:p.Ala531Gly
NM_001354741.1:c.1472C>G	NP_001341670.1:p.Ala491Gly
NM_001354742.1:c.1448C>G	NP_001341671.1:p.Ala483Gly
NM_001354743.1:c.1448C>G	NP_001341672.1:p.Ala483Gly
NM_001354744.1:c.1448C>G	NP_001341673.1:p.Ala483Gly
NM_001354745.1:c.1361C>G	NP_001341674.1:p.Ala454Gly
NM_001354746.1:c.1322C>G	NP_001341675.1:p.Ala441Gly
NM_001354747.1:c.1298C>G	NP_001341676.1:p.Ala433Gly
NM_001354748.1:c.1298C>G	NP_001341677.1:p.Ala433Gly
NM_001363619.1:c.1355C>G	NP_001350548.1:p.Ala452Gly
NR_148954.1:n.1885C>G
NR_148955.1:n.2521C>G
NR_148956.1:n.1811C>G
NR_148957.1:n.2040C>G
NR_148958.1:n.1788C>G
NR_148959.1:n.1714C>G
XM_005268976.3:c.1757C>G	XP_005269033.1:p.Ala586Gly
XM_017019469.1:c.1568C>G	XP_016874958.1:p.Ala523Gly
XM_024449020.1:c.1670C>G	XP_024304788.1:p.Ala557Gly
XM_024449021.1:c.1547C>G	XP_024304789.1:p.Ala516Gly
XM_024449022.1:c.1448C>G	XP_024304790.1:p.Ala483Gly
NM_001166687.2:c.1448C>G	NP_001160159.1:p.Ala483Gly
NM_001166688.2:c.1448C>G	NP_001160160.1:p.Ala483Gly
NM_001354741.2:c.1472C>G	NP_001341670.1:p.Ala491Gly
NM_001354742.2:c.1448C>G	NP_001341671.1:p.Ala483Gly
NM_001354743.2:c.1448C>G	NP_001341672.1:p.Ala483Gly
NM_001354744.2:c.1448C>G	NP_001341673.1:p.Ala483Gly
NM_001354745.2:c.1361C>G	NP_001341674.1:p.Ala454Gly
NM_001354746.2:c.1322C>G	NP_001341675.1:p.Ala441Gly
NM_001354747.2:c.1298C>G	NP_001341676.1:p.Ala433Gly
NM_001354748.2:c.1298C>G	NP_001341677.1:p.Ala433Gly
NM_001363619.2:c.1355C>G	NP_001350548.1:p.Ala452Gly
NR_148954.2:n.1751C>G
NR_148956.2:n.1677C>G
NR_148957.2:n.1906C>G
NR_148958.2:n.1654C>G
NR_148959.2:n.1580C>G