Canonical Allele Identifier: CA384552149

Gene: PFKM

Linked Data

• MyVariant Identifiers: chr12:g.48535605T>G (hg19) ; chr12:g.48141822T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48141822T>G , CM000674.2:g.48141822T>G	GRCh38
NC_000012.11:g.48535605T>G , CM000674.1:g.48535605T>G	GRCh37
NC_000012.10:g.46821872T>G	NCBI36
NG_016199.1:g.40950T>G
NG_016199.2:g.41570T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000550257.7:c.1717T>G	ENSP00000447997.3:p.Phe573Val
ENST00000340802.12:c.1708T>G	ENSP00000345771.6:p.Phe570Val
ENST00000359794.11:c.1495T>G MANE Select	ENSP00000352842.5:p.Phe499Val
ENST00000549941.7:c.1402T>G	ENSP00000446829.3:p.Phe468Val
ENST00000550345.6:c.1495T>G	ENSP00000450369.2:p.Phe499Val
ENST00000550924.6:c.1495T>G	ENSP00000446945.2:p.Phe499Val
ENST00000551339.6:c.1495T>G	ENSP00000448253.2:p.Phe499Val
ENST00000642730.1:c.1804T>G	ENSP00000496597.1:p.Phe602Val
ENST00000312352.11:c.1495T>G	ENSP00000309438.7:p.Phe499Val
ENST00000340802.10:c.1708T>G	ENSP00000345771.6:p.Phe570Val
ENST00000359794.9:c.1495T>G	ENSP00000352842.5:p.Phe499Val
ENST00000546465.1:c.340T>G	ENSP00000446519.1:p.Phe114Val
ENST00000546964.5:n.1819T>G
ENST00000547581.5:c.*1763T>G	ENSP00000447992.1:n.*1763T>G
ENST00000547587.5:c.1495T>G	ENSP00000449426.1:p.Phe499Val
ENST00000550802.1:n.127T>G
ENST00000551804.5:c.1402T>G	ENSP00000448177.1:p.Phe468Val
ENST00000552214.1:n.151T>G
ENST00000552752.5:c.644T>G
ENST00000552818.1:n.118T>G
NM_000289.5:c.1495T>G	NP_000280.1:p.Phe499Val
NM_001166686.1:c.1708T>G	NP_001160158.1:p.Phe570Val
NM_001166687.1:c.1495T>G	NP_001160159.1:p.Phe499Val
NM_001166688.1:c.1495T>G	NP_001160160.1:p.Phe499Val
XM_005268974.1:c.1804T>G	XP_005269031.1:p.Phe602Val
XM_005268975.1:c.1804T>G	XP_005269032.1:p.Phe602Val
XM_005268976.2:c.1804T>G	XP_005269033.1:p.Phe602Val
XM_005268977.1:c.1708T>G	XP_005269034.1:p.Phe570Val
XM_005268978.2:c.1708T>G	XP_005269035.1:p.Phe570Val
XM_005268979.1:c.1708T>G	XP_005269036.1:p.Phe570Val
XM_011538487.1:c.1711T>G	XP_011536789.1:p.Phe571Val
XM_011538488.1:c.1495T>G	XP_011536790.1:p.Phe499Val
NM_000289.6:c.1495T>G MANE Select	NP_000280.1:p.Phe499Val
NM_001166686.2:c.1708T>G	NP_001160158.1:p.Phe570Val
NM_001354735.1:c.1804T>G	NP_001341664.1:p.Phe602Val
NM_001354736.1:c.1804T>G	NP_001341665.1:p.Phe602Val
NM_001354737.1:c.1708T>G	NP_001341666.1:p.Phe570Val
NM_001354738.1:c.1708T>G	NP_001341667.1:p.Phe570Val
NM_001354739.1:c.1708T>G	NP_001341668.1:p.Phe570Val
NM_001354740.1:c.1639T>G	NP_001341669.1:p.Phe547Val
NM_001354741.1:c.1519T>G	NP_001341670.1:p.Phe507Val
NM_001354742.1:c.1495T>G	NP_001341671.1:p.Phe499Val
NM_001354743.1:c.1495T>G	NP_001341672.1:p.Phe499Val
NM_001354744.1:c.1495T>G	NP_001341673.1:p.Phe499Val
NM_001354745.1:c.1408T>G	NP_001341674.1:p.Phe470Val
NM_001354746.1:c.1369T>G	NP_001341675.1:p.Phe457Val
NM_001354747.1:c.1345T>G	NP_001341676.1:p.Phe449Val
NM_001354748.1:c.1345T>G	NP_001341677.1:p.Phe449Val
NM_001363619.1:c.1402T>G	NP_001350548.1:p.Phe468Val
NR_148954.1:n.1932T>G
NR_148955.1:n.2568T>G
NR_148956.1:n.1858T>G
NR_148957.1:n.2087T>G
NR_148958.1:n.1835T>G
NR_148959.1:n.1761T>G
XM_005268976.3:c.1804T>G	XP_005269033.1:p.Phe602Val
XM_017019469.1:c.1615T>G	XP_016874958.1:p.Phe539Val
XM_024449020.1:c.1717T>G	XP_024304788.1:p.Phe573Val
XM_024449021.1:c.1594T>G	XP_024304789.1:p.Phe532Val
XM_024449022.1:c.1495T>G	XP_024304790.1:p.Phe499Val
NM_001166687.2:c.1495T>G	NP_001160159.1:p.Phe499Val
NM_001166688.2:c.1495T>G	NP_001160160.1:p.Phe499Val
NM_001354741.2:c.1519T>G	NP_001341670.1:p.Phe507Val
NM_001354742.2:c.1495T>G	NP_001341671.1:p.Phe499Val
NM_001354743.2:c.1495T>G	NP_001341672.1:p.Phe499Val
NM_001354744.2:c.1495T>G	NP_001341673.1:p.Phe499Val
NM_001354745.2:c.1408T>G	NP_001341674.1:p.Phe470Val
NM_001354746.2:c.1369T>G	NP_001341675.1:p.Phe457Val
NM_001354747.2:c.1345T>G	NP_001341676.1:p.Phe449Val
NM_001354748.2:c.1345T>G	NP_001341677.1:p.Phe449Val
NM_001363619.2:c.1402T>G	NP_001350548.1:p.Phe468Val
NR_148954.2:n.1798T>G
NR_148956.2:n.1724T>G
NR_148957.2:n.1953T>G
NR_148958.2:n.1701T>G
NR_148959.2:n.1627T>G