Canonical Allele Identifier: CA5720768

Gene: FGFR2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121503881G>A , CM000672.2:g.121503881G>A	GRCh38
NC_000010.10:g.123263395G>A , CM000672.1:g.123263395G>A	GRCh37
NC_000010.9:g.123253385G>A	NCBI36
NG_012449.1:g.99578C>T
NG_012449.2:g.99578C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000457416.7:c.1351C>T MANE Plus Clinical	ENSP00000410294.2:p.Arg451Cys
ENST00000351936.11:c.1342C>T	ENSP00000309878.10:p.Arg448Cys
ENST00000638709.2:c.172C>T	ENSP00000491912.2:p.Arg58Cys
ENST00000682296.1:n.690C>T
ENST00000682550.1:c.997C>T	ENSP00000507633.1:p.Arg333Cys
ENST00000682772.1:c.172C>T	ENSP00000506848.1:p.Arg58Cys
ENST00000682904.1:n.168C>T
ENST00000683211.1:c.1342C>T	ENSP00000508257.1:p.Arg448Cys
ENST00000683250.1:c.*50C>T	ENSP00000506847.1:n.*50C>T
ENST00000683418.1:n.3689C>T
ENST00000684153.1:c.997C>T	ENSP00000506937.1:p.Arg333Cys
ENST00000684516.1:n.2361C>T
ENST00000358487.10:c.1348C>T MANE Select	ENSP00000351276.6:p.Arg450Cys
ENST00000336553.10:c.1075C>T	ENSP00000337665.6:p.Arg359Cys
ENST00000346997.6:c.1342C>T	ENSP00000263451.5:p.Arg448Cys
ENST00000351936.10:c.1348C>T	ENSP00000309878.9:p.Arg450Cys
ENST00000356226.8:c.997C>T	ENSP00000348559.4:p.Arg333Cys
ENST00000357555.9:c.1081C>T	ENSP00000350166.5:p.Arg361Cys
ENST00000358487.9:c.1348C>T	ENSP00000351276.5:p.Arg450Cys
ENST00000360144.7:c.1084C>T	ENSP00000353262.3:p.Arg362Cys
ENST00000369056.5:c.1351C>T	ENSP00000358052.1:p.Arg451Cys
ENST00000369058.7:c.1351C>T	ENSP00000358054.3:p.Arg451Cys
ENST00000369059.5:c.1006C>T	ENSP00000358055.1:p.Arg336Cys
ENST00000369060.8:c.1000C>T	ENSP00000358056.4:p.Arg334Cys
ENST00000369061.8:c.1012C>T	ENSP00000358057.4:p.Arg338Cys
ENST00000429361.5:c.124C>T	ENSP00000404219.1:p.Arg42Cys
ENST00000457416.6:c.1351C>T	ENSP00000410294.2:p.Arg451Cys
ENST00000478859.5:c.664C>T	ENSP00000474011.1:p.Arg222Cys
ENST00000604236.5:c.*395C>T	ENSP00000474109.1:n.*395C>T
ENST00000613048.4:c.1081C>T	ENSP00000484154.1:p.Arg361Cys
NM_000141.4:c.1348C>T	NP_000132.3:p.Arg450Cys
NM_001144913.1:c.1351C>T	NP_001138385.1:p.Arg451Cys
NM_001144914.1:c.1012C>T	NP_001138386.1:p.Arg338Cys
NM_001144915.1:c.1081C>T	NP_001138387.1:p.Arg361Cys
NM_001144916.1:c.1003C>T	NP_001138388.1:p.Arg335Cys
NM_001144917.1:c.1000C>T	NP_001138389.1:p.Arg334Cys
NM_001144918.1:c.997C>T	NP_001138390.1:p.Arg333Cys
NM_001144919.1:c.1084C>T	NP_001138391.1:p.Arg362Cys
NM_022970.3:c.1351C>T	NP_075259.4:p.Arg451Cys
NM_023029.2:c.1081C>T	NP_075418.1:p.Arg361Cys
NR_073009.1:n.1798C>T
XM_006717708.2:c.1402C>T	XP_006717771.1:p.Arg468Cys
XM_006717709.2:c.1399C>T	XP_006717772.1:p.Arg467Cys
XM_006717710.2:c.1408C>T	XP_006717773.1:p.Arg470Cys
XM_006717711.2:c.1141C>T	XP_006717774.1:p.Arg381Cys
XM_006717712.2:c.1063C>T	XP_006717775.1:p.Arg355Cys
XM_006717713.2:c.1405C>T	XP_006717776.1:p.Arg469Cys
XM_011539510.1:c.664C>T	XP_011537812.1:p.Arg222Cys
NM_001320654.1:c.664C>T	NP_001307583.1:p.Arg222Cys
NM_001320658.1:c.1342C>T	NP_001307587.1:p.Arg448Cys
XM_006717708.3:c.1402C>T	XP_006717771.1:p.Arg468Cys
XM_006717710.4:c.1408C>T	XP_006717773.1:p.Arg470Cys
XM_017015920.2:c.1402C>T	XP_016871409.1:p.Arg468Cys
XM_017015921.2:c.1399C>T	XP_016871410.1:p.Arg467Cys
XM_017015924.2:c.1060C>T	XP_016871413.1:p.Arg354Cys
XM_017015925.2:c.1054C>T	XP_016871414.1:p.Arg352Cys
XM_024447887.1:c.1138C>T	XP_024303655.1:p.Arg380Cys
XM_024447888.1:c.1135C>T	XP_024303656.1:p.Arg379Cys
XM_024447889.1:c.1132C>T	XP_024303657.1:p.Arg378Cys
XM_024447890.1:c.1141C>T	XP_024303658.1:p.Arg381Cys
XM_024447891.1:c.1063C>T	XP_024303659.1:p.Arg355Cys
XM_024447892.1:c.178C>T	XP_024303660.1:p.Arg60Cys
NM_000141.5:c.1348C>T MANE Select	NP_000132.3:p.Arg450Cys
NM_001144917.2:c.1000C>T	NP_001138389.1:p.Arg334Cys
NM_001144918.2:c.997C>T	NP_001138390.1:p.Arg333Cys
NM_001144919.2:c.1084C>T	NP_001138391.1:p.Arg362Cys
NM_001320658.2:c.1342C>T	NP_001307587.1:p.Arg448Cys
NR_073009.2:n.1784C>T
NM_001144915.2:c.1081C>T	NP_001138387.1:p.Arg361Cys
NM_001144916.2:c.1003C>T	NP_001138388.1:p.Arg335Cys
NM_001320654.2:c.664C>T	NP_001307583.1:p.Arg222Cys