Canonical Allele Identifier: CA378313388

Gene: FGFR2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121487423C>T , CM000672.2:g.121487423C>T	GRCh38
NC_000010.10:g.123246937C>T , CM000672.1:g.123246937C>T	GRCh37
NC_000010.9:g.123236927C>T	NCBI36
NG_012449.1:g.116036G>A
NG_012449.2:g.116036G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000141.5:c.1988G>A MANE Select	NP_000132.3:p.Gly663Glu
ENST00000358487.10:c.1988G>A MANE Select	ENSP00000351276.6:p.Gly663Glu
ENST00000457416.7:c.1991G>A MANE Plus Clinical	ENSP00000410294.2:p.Gly664Glu
NM_000141.4:c.1988G>A	NP_000132.3:p.Gly663Glu
NM_001144913.1:c.1991G>A	NP_001138385.1:p.Gly664Glu
NM_001144914.1:c.1652G>A	NP_001138386.1:p.Gly551Glu
NM_001144915.1:c.1721G>A	NP_001138387.1:p.Gly574Glu
NM_001144915.2:c.1721G>A	NP_001138387.1:p.Gly574Glu
NM_001144916.1:c.1643G>A	NP_001138388.1:p.Gly548Glu
NM_001144916.2:c.1643G>A	NP_001138388.1:p.Gly548Glu
NM_001144917.1:c.1640G>A	NP_001138389.1:p.Gly547Glu
NM_001144917.2:c.1640G>A	NP_001138389.1:p.Gly547Glu
NM_001144918.1:c.1637G>A	NP_001138390.1:p.Gly546Glu
NM_001144918.2:c.1637G>A	NP_001138390.1:p.Gly546Glu
NM_001144919.1:c.1724G>A	NP_001138391.1:p.Gly575Glu
NM_001144919.2:c.1724G>A	NP_001138391.1:p.Gly575Glu
NM_001320654.1:c.1304G>A	NP_001307583.1:p.Gly435Glu
NM_001320654.2:c.1304G>A	NP_001307583.1:p.Gly435Glu
NM_001320658.1:c.1982G>A	NP_001307587.1:p.Gly661Glu
NM_001320658.2:c.1982G>A	NP_001307587.1:p.Gly661Glu
NM_022970.3:c.1991G>A	NP_075259.4:p.Gly664Glu
NM_023029.2:c.1721G>A	NP_075418.1:p.Gly574Glu
NR_073009.1:n.2438G>A
NR_073009.2:n.2424G>A
ENST00000336553.10:c.1715G>A	ENSP00000337665.6:p.Gly572Glu
ENST00000346997.6:c.1982G>A	ENSP00000263451.5:p.Gly661Glu
ENST00000351936.10:c.1988G>A	ENSP00000309878.9:p.Gly663Glu
ENST00000351936.11:c.1982G>A	ENSP00000309878.10:p.Gly661Glu
ENST00000356226.8:c.1637G>A	ENSP00000348559.4:p.Gly546Glu
ENST00000357555.9:c.1721G>A	ENSP00000350166.5:p.Gly574Glu
ENST00000358487.9:c.1988G>A	ENSP00000351276.5:p.Gly663Glu
ENST00000360144.7:c.1724G>A	ENSP00000353262.3:p.Gly575Glu
ENST00000369056.5:c.1991G>A	ENSP00000358052.1:p.Gly664Glu
ENST00000369058.7:c.1991G>A	ENSP00000358054.3:p.Gly664Glu
ENST00000369059.5:c.1646G>A	ENSP00000358055.1:p.Gly549Glu
ENST00000369060.8:c.1640G>A	ENSP00000358056.4:p.Gly547Glu
ENST00000369061.8:c.1652G>A	ENSP00000358057.4:p.Gly551Glu
ENST00000429361.5:c.764G>A	ENSP00000404219.1:p.Gly255Glu
ENST00000457416.6:c.1991G>A	ENSP00000410294.2:p.Gly664Glu
ENST00000478859.5:c.1304G>A	ENSP00000474011.1:p.Gly435Glu
ENST00000604236.5:c.*1035G>A	ENSP00000474109.1:n.*1035G>A
ENST00000613048.4:c.1721G>A	ENSP00000484154.1:p.Gly574Glu
ENST00000638709.2:c.812G>A	ENSP00000491912.2:p.Gly271Glu
ENST00000682296.1:n.1330G>A
ENST00000682550.1:c.1637G>A	ENSP00000507633.1:p.Gly546Glu
ENST00000682772.1:c.812G>A	ENSP00000506848.1:p.Gly271Glu
ENST00000682904.1:n.808G>A
ENST00000683029.1:n.400G>A
ENST00000683211.1:c.1982G>A	ENSP00000508257.1:p.Gly661Glu
ENST00000683250.1:c.*690G>A	ENSP00000506847.1:n.*690G>A
ENST00000683418.1:n.4329G>A
ENST00000684153.1:c.1637G>A	ENSP00000506937.1:p.Gly546Glu
ENST00000684516.1:n.3001G>A
XM_006717708.2:c.2042G>A	XP_006717771.1:p.Gly681Glu
XM_006717708.3:c.2042G>A	XP_006717771.1:p.Gly681Glu
XM_006717709.2:c.2039G>A	XP_006717772.1:p.Gly680Glu
XM_006717710.2:c.2048G>A	XP_006717773.1:p.Gly683Glu
XM_006717710.4:c.2048G>A	XP_006717773.1:p.Gly683Glu
XM_006717711.2:c.1781G>A	XP_006717774.1:p.Gly594Glu
XM_006717712.2:c.1703G>A	XP_006717775.1:p.Gly568Glu
XM_006717713.2:c.2045G>A	XP_006717776.1:p.Gly682Glu
XM_011539510.1:c.1304G>A	XP_011537812.1:p.Gly435Glu
XM_017015920.2:c.2042G>A	XP_016871409.1:p.Gly681Glu
XM_017015921.2:c.2039G>A	XP_016871410.1:p.Gly680Glu
XM_017015924.2:c.1700G>A	XP_016871413.1:p.Gly567Glu
XM_017015925.2:c.1694G>A	XP_016871414.1:p.Gly565Glu
XM_024447887.1:c.1778G>A	XP_024303655.1:p.Gly593Glu
XM_024447888.1:c.1775G>A	XP_024303656.1:p.Gly592Glu
XM_024447889.1:c.1772G>A	XP_024303657.1:p.Gly591Glu
XM_024447890.1:c.1781G>A	XP_024303658.1:p.Gly594Glu
XM_024447891.1:c.1703G>A	XP_024303659.1:p.Gly568Glu
XM_024447892.1:c.818G>A	XP_024303660.1:p.Gly273Glu