Canonical Allele Identifier: CA384551772

Gene: PFKM

Linked Data

• MyVariant Identifiers: chr12:g.48535557G>C (hg19) ; chr12:g.48141774G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48141774G>C , CM000674.2:g.48141774G>C	GRCh38
NC_000012.11:g.48535557G>C , CM000674.1:g.48535557G>C	GRCh37
NC_000012.10:g.46821824G>C	NCBI36
NG_016199.1:g.40902G>C
NG_016199.2:g.41522G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000550257.7:c.1669G>C	ENSP00000447997.3:p.Ala557Pro
ENST00000340802.12:c.1660G>C	ENSP00000345771.6:p.Ala554Pro
ENST00000359794.11:c.1447G>C MANE Select	ENSP00000352842.5:p.Ala483Pro
ENST00000549941.7:c.1354G>C	ENSP00000446829.3:p.Ala452Pro
ENST00000550345.6:c.1447G>C	ENSP00000450369.2:p.Ala483Pro
ENST00000550924.6:c.1447G>C	ENSP00000446945.2:p.Ala483Pro
ENST00000551339.6:c.1447G>C	ENSP00000448253.2:p.Ala483Pro
ENST00000642730.1:c.1756G>C	ENSP00000496597.1:p.Ala586Pro
ENST00000312352.11:c.1447G>C	ENSP00000309438.7:p.Ala483Pro
ENST00000340802.10:c.1660G>C	ENSP00000345771.6:p.Ala554Pro
ENST00000359794.9:c.1447G>C	ENSP00000352842.5:p.Ala483Pro
ENST00000546465.1:c.292G>C	ENSP00000446519.1:p.Ala98Pro
ENST00000546964.5:n.1771G>C
ENST00000547581.5:c.*1715G>C	ENSP00000447992.1:n.*1715G>C
ENST00000547587.5:c.1447G>C	ENSP00000449426.1:p.Ala483Pro
ENST00000550802.1:n.79G>C
ENST00000551804.5:c.1354G>C	ENSP00000448177.1:p.Ala452Pro
ENST00000552214.1:n.103G>C
ENST00000552752.5:c.596G>C
ENST00000552818.1:n.70G>C
NM_000289.5:c.1447G>C	NP_000280.1:p.Ala483Pro
NM_001166686.1:c.1660G>C	NP_001160158.1:p.Ala554Pro
NM_001166687.1:c.1447G>C	NP_001160159.1:p.Ala483Pro
NM_001166688.1:c.1447G>C	NP_001160160.1:p.Ala483Pro
XM_005268974.1:c.1756G>C	XP_005269031.1:p.Ala586Pro
XM_005268975.1:c.1756G>C	XP_005269032.1:p.Ala586Pro
XM_005268976.2:c.1756G>C	XP_005269033.1:p.Ala586Pro
XM_005268977.1:c.1660G>C	XP_005269034.1:p.Ala554Pro
XM_005268978.2:c.1660G>C	XP_005269035.1:p.Ala554Pro
XM_005268979.1:c.1660G>C	XP_005269036.1:p.Ala554Pro
XM_011538487.1:c.1663G>C	XP_011536789.1:p.Ala555Pro
XM_011538488.1:c.1447G>C	XP_011536790.1:p.Ala483Pro
NM_000289.6:c.1447G>C MANE Select	NP_000280.1:p.Ala483Pro
NM_001166686.2:c.1660G>C	NP_001160158.1:p.Ala554Pro
NM_001354735.1:c.1756G>C	NP_001341664.1:p.Ala586Pro
NM_001354736.1:c.1756G>C	NP_001341665.1:p.Ala586Pro
NM_001354737.1:c.1660G>C	NP_001341666.1:p.Ala554Pro
NM_001354738.1:c.1660G>C	NP_001341667.1:p.Ala554Pro
NM_001354739.1:c.1660G>C	NP_001341668.1:p.Ala554Pro
NM_001354740.1:c.1591G>C	NP_001341669.1:p.Ala531Pro
NM_001354741.1:c.1471G>C	NP_001341670.1:p.Ala491Pro
NM_001354742.1:c.1447G>C	NP_001341671.1:p.Ala483Pro
NM_001354743.1:c.1447G>C	NP_001341672.1:p.Ala483Pro
NM_001354744.1:c.1447G>C	NP_001341673.1:p.Ala483Pro
NM_001354745.1:c.1360G>C	NP_001341674.1:p.Ala454Pro
NM_001354746.1:c.1321G>C	NP_001341675.1:p.Ala441Pro
NM_001354747.1:c.1297G>C	NP_001341676.1:p.Ala433Pro
NM_001354748.1:c.1297G>C	NP_001341677.1:p.Ala433Pro
NM_001363619.1:c.1354G>C	NP_001350548.1:p.Ala452Pro
NR_148954.1:n.1884G>C
NR_148955.1:n.2520G>C
NR_148956.1:n.1810G>C
NR_148957.1:n.2039G>C
NR_148958.1:n.1787G>C
NR_148959.1:n.1713G>C
XM_005268976.3:c.1756G>C	XP_005269033.1:p.Ala586Pro
XM_017019469.1:c.1567G>C	XP_016874958.1:p.Ala523Pro
XM_024449020.1:c.1669G>C	XP_024304788.1:p.Ala557Pro
XM_024449021.1:c.1546G>C	XP_024304789.1:p.Ala516Pro
XM_024449022.1:c.1447G>C	XP_024304790.1:p.Ala483Pro
NM_001166687.2:c.1447G>C	NP_001160159.1:p.Ala483Pro
NM_001166688.2:c.1447G>C	NP_001160160.1:p.Ala483Pro
NM_001354741.2:c.1471G>C	NP_001341670.1:p.Ala491Pro
NM_001354742.2:c.1447G>C	NP_001341671.1:p.Ala483Pro
NM_001354743.2:c.1447G>C	NP_001341672.1:p.Ala483Pro
NM_001354744.2:c.1447G>C	NP_001341673.1:p.Ala483Pro
NM_001354745.2:c.1360G>C	NP_001341674.1:p.Ala454Pro
NM_001354746.2:c.1321G>C	NP_001341675.1:p.Ala441Pro
NM_001354747.2:c.1297G>C	NP_001341676.1:p.Ala433Pro
NM_001354748.2:c.1297G>C	NP_001341677.1:p.Ala433Pro
NM_001363619.2:c.1354G>C	NP_001350548.1:p.Ala452Pro
NR_148954.2:n.1750G>C
NR_148956.2:n.1676G>C
NR_148957.2:n.1905G>C
NR_148958.2:n.1653G>C
NR_148959.2:n.1579G>C