Canonical Allele Identifier: CA1941023783

Gene: FGFR2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121515360_121515362delinsCAT , CM000672.2:g.121515360_121515362delinsCAT	GRCh38
NC_000010.10:g.123274874_123274876delinsCAT , CM000672.1:g.123274874_123274876delinsCAT	GRCh37
NC_000010.9:g.123264864_123264866delinsCAT	NCBI36
NG_012449.1:g.88097_88099delinsATG
NG_012449.2:g.88097_88099delinsATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000457416.7:c.1088-43_1088-41delinsATG MANE Plus Clinical	ENSP00000410294.2:n.1088-43_1088-41delinsATG
ENST00000351936.11:c.1085-43_1085-41delinsATG	ENSP00000309878.10:n.1085-43_1085-41delinsATG
ENST00000638709.2:c.-86-43_-86-41delinsATG	ENSP00000491912.2:n.-86-43_-86-41delinsATG
ENST00000682296.1:n.433-43_433-41delinsATG
ENST00000682550.1:c.740-43_740-41delinsATG	ENSP00000507633.1:n.740-43_740-41delinsATG
ENST00000682772.1:c.-86-43_-86-41delinsATG	ENSP00000506848.1:n.-86-43_-86-41delinsATG
ENST00000683211.1:c.1085-43_1085-41delinsATG	ENSP00000508257.1:n.1085-43_1085-41delinsATG
ENST00000683250.1:c.404-11421_404-11419delinsATG	ENSP00000506847.1:n.404-11421_404-11419delinsATG
ENST00000683418.1:n.3432-43_3432-41delinsATG
ENST00000684153.1:c.740-43_740-41delinsATG	ENSP00000506937.1:n.740-43_740-41delinsATG
ENST00000358487.10:c.1085-43_1085-41delinsATG MANE Select	ENSP00000351276.6:n.1085-43_1085-41delinsATG
ENST00000336553.10:c.818-43_818-41delinsATG	ENSP00000337665.6:n.818-43_818-41delinsATG
ENST00000346997.6:c.1085-43_1085-41delinsATG	ENSP00000263451.5:n.1085-43_1085-41delinsATG
ENST00000351936.10:c.1091-43_1091-41delinsATG	ENSP00000309878.9:n.1091-43_1091-41delinsATG
ENST00000356226.8:c.740-43_740-41delinsATG	ENSP00000348559.4:n.740-43_740-41delinsATG
ENST00000357555.9:c.818-43_818-41delinsATG	ENSP00000350166.5:n.818-43_818-41delinsATG
ENST00000358487.9:c.1085-43_1085-41delinsATG	ENSP00000351276.5:n.1085-43_1085-41delinsATG
ENST00000360144.7:c.821-43_821-41delinsATG	ENSP00000353262.3:n.821-43_821-41delinsATG
ENST00000369056.5:c.1088-43_1088-41delinsATG	ENSP00000358052.1:n.1088-43_1088-41delinsATG
ENST00000369058.7:c.1088-43_1088-41delinsATG	ENSP00000358054.3:n.1088-43_1088-41delinsATG
ENST00000369059.5:c.743-43_743-41delinsATG	ENSP00000358055.1:n.743-43_743-41delinsATG
ENST00000369060.8:c.939+4617_939+4619delinsATG	ENSP00000358056.4:n.939+4617_939+4619delinsATG
ENST00000369061.8:c.749-43_749-41delinsATG	ENSP00000358057.4:n.749-43_749-41delinsATG
ENST00000457416.6:c.1088-43_1088-41delinsATG	ENSP00000410294.2:n.1088-43_1088-41delinsATG
ENST00000463870.5:n.294-43_294-41delinsATG
ENST00000478859.5:c.401-43_401-41delinsATG	ENSP00000474011.1:n.401-43_401-41delinsATG
ENST00000604236.5:c.*132-43_*132-41delinsATG	ENSP00000474109.1:n.*132-43_*132-41delinsATG
ENST00000613048.4:c.818-43_818-41delinsATG	ENSP00000484154.1:n.818-43_818-41delinsATG
NM_000141.4:c.1085-43_1085-41delinsATG	NP_000132.3:n.1085-43_1085-41delinsATG
NM_001144913.1:c.1088-43_1088-41delinsATG	NP_001138385.1:n.1088-43_1088-41delinsATG
NM_001144914.1:c.749-43_749-41delinsATG	NP_001138386.1:n.749-43_749-41delinsATG
NM_001144915.1:c.818-43_818-41delinsATG	NP_001138387.1:n.818-43_818-41delinsATG
NM_001144916.1:c.740-43_740-41delinsATG	NP_001138388.1:n.740-43_740-41delinsATG
NM_001144917.1:c.939+4617_939+4619delinsATG	NP_001138389.1:n.939+4617_939+4619delinsATG
NM_001144918.1:c.740-43_740-41delinsATG	NP_001138390.1:n.740-43_740-41delinsATG
NM_001144919.1:c.821-43_821-41delinsATG	NP_001138391.1:n.821-43_821-41delinsATG
NM_022970.3:c.1088-43_1088-41delinsATG	NP_075259.4:n.1088-43_1088-41delinsATG
NM_023029.2:c.818-43_818-41delinsATG	NP_075418.1:n.818-43_818-41delinsATG
NR_073009.1:n.1535-43_1535-41delinsATG
XM_006717708.2:c.1145-43_1145-41delinsATG	XP_006717771.1:n.1145-43_1145-41delinsATG
XM_006717709.2:c.1142-43_1142-41delinsATG	XP_006717772.1:n.1142-43_1142-41delinsATG
XM_006717710.2:c.1145-43_1145-41delinsATG	XP_006717773.1:n.1145-43_1145-41delinsATG
XM_006717711.2:c.878-43_878-41delinsATG	XP_006717774.1:n.878-43_878-41delinsATG
XM_006717712.2:c.800-43_800-41delinsATG	XP_006717775.1:n.800-43_800-41delinsATG
XM_006717713.2:c.1142-43_1142-41delinsATG	XP_006717776.1:n.1142-43_1142-41delinsATG
XM_011539510.1:c.401-43_401-41delinsATG	XP_011537812.1:n.401-43_401-41delinsATG
NM_001320654.1:c.401-43_401-41delinsATG	NP_001307583.1:n.401-43_401-41delinsATG
NM_001320658.1:c.1085-43_1085-41delinsATG	NP_001307587.1:n.1085-43_1085-41delinsATG
XM_006717708.3:c.1145-43_1145-41delinsATG	XP_006717771.1:n.1145-43_1145-41delinsATG
XM_006717710.4:c.1145-43_1145-41delinsATG	XP_006717773.1:n.1145-43_1145-41delinsATG
XM_017015920.2:c.1145-43_1145-41delinsATG	XP_016871409.1:n.1145-43_1145-41delinsATG
XM_017015921.2:c.1142-43_1142-41delinsATG	XP_016871410.1:n.1142-43_1142-41delinsATG
XM_017015924.2:c.797-43_797-41delinsATG	XP_016871413.1:n.797-43_797-41delinsATG
XM_017015925.2:c.797-43_797-41delinsATG	XP_016871414.1:n.797-43_797-41delinsATG
XM_024447887.1:c.875-43_875-41delinsATG	XP_024303655.1:n.875-43_875-41delinsATG
XM_024447888.1:c.878-43_878-41delinsATG	XP_024303656.1:n.878-43_878-41delinsATG
XM_024447889.1:c.875-43_875-41delinsATG	XP_024303657.1:n.875-43_875-41delinsATG
XM_024447890.1:c.878-43_878-41delinsATG	XP_024303658.1:n.878-43_878-41delinsATG
XM_024447891.1:c.800-43_800-41delinsATG	XP_024303659.1:n.800-43_800-41delinsATG
XM_024447892.1:c.-86-43_-86-41delinsATG	XP_024303660.1:n.-86-43_-86-41delinsATG
NM_000141.5:c.1085-43_1085-41delinsATG MANE Select	NP_000132.3:n.1085-43_1085-41delinsATG
NM_001144917.2:c.939+4617_939+4619delinsATG	NP_001138389.1:n.939+4617_939+4619delinsATG
NM_001144918.2:c.740-43_740-41delinsATG	NP_001138390.1:n.740-43_740-41delinsATG
NM_001144919.2:c.821-43_821-41delinsATG	NP_001138391.1:n.821-43_821-41delinsATG
NM_001320658.2:c.1085-43_1085-41delinsATG	NP_001307587.1:n.1085-43_1085-41delinsATG
NR_073009.2:n.1521-43_1521-41delinsATG
NM_001144915.2:c.818-43_818-41delinsATG	NP_001138387.1:n.818-43_818-41delinsATG
NM_001144916.2:c.740-43_740-41delinsATG	NP_001138388.1:n.740-43_740-41delinsATG
NM_001320654.2:c.401-43_401-41delinsATG	NP_001307583.1:n.401-43_401-41delinsATG