Canonical Allele Identifier: CA471647194

Gene: FGFR2

Linked Data

• MyVariant Identifiers: chr10:g.123247508G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121487994G>C , CM000672.2:g.121487994G>C	GRCh38
NC_000010.10:g.123247508G>C , CM000672.1:g.123247508G>C	GRCh37
NC_000010.9:g.123237498G>C	NCBI36
NG_012449.1:g.115465C>G
NG_012449.2:g.115465C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000457416.7:c.1986C>G MANE Plus Clinical	ENSP00000410294.2:p.Thr662=
ENST00000351936.11:c.1977C>G	ENSP00000309878.10:p.Thr659=
ENST00000638709.2:c.807C>G	ENSP00000491912.2:p.Thr269=
ENST00000682296.1:n.1325C>G
ENST00000682550.1:c.1632C>G	ENSP00000507633.1:p.Thr544=
ENST00000682772.1:c.807C>G	ENSP00000506848.1:p.Thr269=
ENST00000682904.1:n.803C>G
ENST00000683029.1:n.395C>G
ENST00000683211.1:c.1977C>G	ENSP00000508257.1:p.Thr659=
ENST00000683250.1:c.*685C>G	ENSP00000506847.1:n.*685C>G
ENST00000683418.1:n.4324C>G
ENST00000684153.1:c.1632C>G	ENSP00000506937.1:p.Thr544=
ENST00000684516.1:n.2996C>G
ENST00000358487.10:c.1983C>G MANE Select	ENSP00000351276.6:p.Thr661=
ENST00000336553.10:c.1710C>G	ENSP00000337665.6:p.Thr570=
ENST00000346997.6:c.1977C>G	ENSP00000263451.5:p.Thr659=
ENST00000351936.10:c.1983C>G	ENSP00000309878.9:p.Thr661=
ENST00000356226.8:c.1632C>G	ENSP00000348559.4:p.Thr544=
ENST00000357555.9:c.1716C>G	ENSP00000350166.5:p.Thr572=
ENST00000358487.9:c.1983C>G	ENSP00000351276.5:p.Thr661=
ENST00000360144.7:c.1719C>G	ENSP00000353262.3:p.Thr573=
ENST00000369056.5:c.1986C>G	ENSP00000358052.1:p.Thr662=
ENST00000369058.7:c.1986C>G	ENSP00000358054.3:p.Thr662=
ENST00000369059.5:c.1641C>G	ENSP00000358055.1:p.Thr547=
ENST00000369060.8:c.1635C>G	ENSP00000358056.4:p.Thr545=
ENST00000369061.8:c.1647C>G	ENSP00000358057.4:p.Thr549=
ENST00000429361.5:c.759C>G	ENSP00000404219.1:p.Thr253=
ENST00000457416.6:c.1986C>G	ENSP00000410294.2:p.Thr662=
ENST00000478859.5:c.1299C>G	ENSP00000474011.1:p.Thr433=
ENST00000604236.5:c.*1030C>G	ENSP00000474109.1:n.*1030C>G
ENST00000613048.4:c.1716C>G	ENSP00000484154.1:p.Thr572=
NM_000141.4:c.1983C>G	NP_000132.3:p.Thr661=
NM_001144913.1:c.1986C>G	NP_001138385.1:p.Thr662=
NM_001144914.1:c.1647C>G	NP_001138386.1:p.Thr549=
NM_001144915.1:c.1716C>G	NP_001138387.1:p.Thr572=
NM_001144916.1:c.1638C>G	NP_001138388.1:p.Thr546=
NM_001144917.1:c.1635C>G	NP_001138389.1:p.Thr545=
NM_001144918.1:c.1632C>G	NP_001138390.1:p.Thr544=
NM_001144919.1:c.1719C>G	NP_001138391.1:p.Thr573=
NM_022970.3:c.1986C>G	NP_075259.4:p.Thr662=
NM_023029.2:c.1716C>G	NP_075418.1:p.Thr572=
NR_073009.1:n.2433C>G
XM_006717708.2:c.2037C>G	XP_006717771.1:p.Thr679=
XM_006717709.2:c.2034C>G	XP_006717772.1:p.Thr678=
XM_006717710.2:c.2043C>G	XP_006717773.1:p.Thr681=
XM_006717711.2:c.1776C>G	XP_006717774.1:p.Thr592=
XM_006717712.2:c.1698C>G	XP_006717775.1:p.Thr566=
XM_006717713.2:c.2040C>G	XP_006717776.1:p.Thr680=
XM_011539510.1:c.1299C>G	XP_011537812.1:p.Thr433=
NM_001320654.1:c.1299C>G	NP_001307583.1:p.Thr433=
NM_001320658.1:c.1977C>G	NP_001307587.1:p.Thr659=
XM_006717708.3:c.2037C>G	XP_006717771.1:p.Thr679=
XM_006717710.4:c.2043C>G	XP_006717773.1:p.Thr681=
XM_017015920.2:c.2037C>G	XP_016871409.1:p.Thr679=
XM_017015921.2:c.2034C>G	XP_016871410.1:p.Thr678=
XM_017015924.2:c.1695C>G	XP_016871413.1:p.Thr565=
XM_017015925.2:c.1689C>G	XP_016871414.1:p.Thr563=
XM_024447887.1:c.1773C>G	XP_024303655.1:p.Thr591=
XM_024447888.1:c.1770C>G	XP_024303656.1:p.Thr590=
XM_024447889.1:c.1767C>G	XP_024303657.1:p.Thr589=
XM_024447890.1:c.1776C>G	XP_024303658.1:p.Thr592=
XM_024447891.1:c.1698C>G	XP_024303659.1:p.Thr566=
XM_024447892.1:c.813C>G	XP_024303660.1:p.Thr271=
NM_000141.5:c.1983C>G MANE Select	NP_000132.3:p.Thr661=
NM_001144917.2:c.1635C>G	NP_001138389.1:p.Thr545=
NM_001144918.2:c.1632C>G	NP_001138390.1:p.Thr544=
NM_001144919.2:c.1719C>G	NP_001138391.1:p.Thr573=
NM_001320658.2:c.1977C>G	NP_001307587.1:p.Thr659=
NR_073009.2:n.2419C>G
NM_001144915.2:c.1716C>G	NP_001138387.1:p.Thr572=
NM_001144916.2:c.1638C>G	NP_001138388.1:p.Thr546=
NM_001320654.2:c.1299C>G	NP_001307583.1:p.Thr433=