Canonical Allele Identifier: CA1941025812

Gene: FGFR2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121519975_121519976delinsTC , CM000672.2:g.121519975_121519976delinsTC	GRCh38
NC_000010.10:g.123279489_123279490delinsTC , CM000672.1:g.123279489_123279490delinsTC	GRCh37
NC_000010.9:g.123269479_123269480delinsTC	NCBI36
NG_012449.1:g.83483_83484delinsGA
NG_012449.2:g.83483_83484delinsGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000457416.7:c.939+3_939+4delinsGA MANE Plus Clinical	ENSP00000410294.2:n.939+3_939+4delinsGA
ENST00000351936.11:c.939+3_939+4delinsGA	ENSP00000309878.10:n.939+3_939+4delinsGA
ENST00000638709.2:c.-232+3_-232+4delinsGA	ENSP00000491912.2:n.-232+3_-232+4delinsGA...
ENST00000682296.1:n.287+3_287+4delinsGA
ENST00000682400.1:n.594+3_594+4delinsGA
ENST00000682550.1:c.594+3_594+4delinsGA	ENSP00000507633.1:n.594+3_594+4delinsGA
ENST00000682772.1:c.-232+3_-232+4delinsGA	ENSP00000506848.1:n.-232+3_-232+4delinsGA...
ENST00000683211.1:c.939+3_939+4delinsGA	ENSP00000508257.1:n.939+3_939+4delinsGA
ENST00000683250.1:c.404-16035_404-16034delinsGA	ENSP00000506847.1:n.404-16035_404-16034de...
ENST00000683418.1:n.3286+3_3286+4delinsGA
ENST00000683678.1:n.939+3_939+4delinsGA
ENST00000684153.1:c.594+3_594+4delinsGA	ENSP00000506937.1:n.594+3_594+4delinsGA
ENST00000358487.10:c.939+3_939+4delinsGA MANE Select	ENSP00000351276.6:n.939+3_939+4delinsGA
ENST00000336553.10:c.672+3_672+4delinsGA	ENSP00000337665.6:n.672+3_672+4delinsGA
ENST00000346997.6:c.939+3_939+4delinsGA	ENSP00000263451.5:n.939+3_939+4delinsGA
ENST00000351936.10:c.939+3_939+4delinsGA	ENSP00000309878.9:n.939+3_939+4delinsGA
ENST00000356226.8:c.594+3_594+4delinsGA	ENSP00000348559.4:n.594+3_594+4delinsGA
ENST00000357555.9:c.672+3_672+4delinsGA	ENSP00000350166.5:n.672+3_672+4delinsGA
ENST00000358487.9:c.939+3_939+4delinsGA	ENSP00000351276.5:n.939+3_939+4delinsGA
ENST00000360144.7:c.672+3_672+4delinsGA	ENSP00000353262.3:n.672+3_672+4delinsGA
ENST00000369056.5:c.939+3_939+4delinsGA	ENSP00000358052.1:n.939+3_939+4delinsGA
ENST00000369058.7:c.939+3_939+4delinsGA	ENSP00000358054.3:n.939+3_939+4delinsGA
ENST00000369059.5:c.594+3_594+4delinsGA	ENSP00000358055.1:n.594+3_594+4delinsGA
ENST00000369060.8:c.939+3_939+4delinsGA	ENSP00000358056.4:n.939+3_939+4delinsGA
ENST00000369061.8:c.749-4657_749-4656delinsGA	ENSP00000358057.4:n.749-4657_749-4656deli...
ENST00000457416.6:c.939+3_939+4delinsGA	ENSP00000410294.2:n.939+3_939+4delinsGA
ENST00000478859.5:c.255+3_255+4delinsGA	ENSP00000474011.1:n.255+3_255+4delinsGA
ENST00000490349.5:n.1200+3_1200+4delinsGA
ENST00000604236.5:c.594+3_594+4delinsGA	ENSP00000474109.1:n.594+3_594+4delinsGA
ENST00000613048.4:c.672+3_672+4delinsGA	ENSP00000484154.1:n.672+3_672+4delinsGA
NM_000141.4:c.939+3_939+4delinsGA	NP_000132.3:n.939+3_939+4delinsGA
NM_001144913.1:c.939+3_939+4delinsGA	NP_001138385.1:n.939+3_939+4delinsGA
NM_001144914.1:c.749-4657_749-4656delinsGA	NP_001138386.1:n.749-4657_749-4656delinsG...
NM_001144915.1:c.672+3_672+4delinsGA	NP_001138387.1:n.672+3_672+4delinsGA
NM_001144916.1:c.594+3_594+4delinsGA	NP_001138388.1:n.594+3_594+4delinsGA
NM_001144917.1:c.939+3_939+4delinsGA	NP_001138389.1:n.939+3_939+4delinsGA
NM_001144918.1:c.594+3_594+4delinsGA	NP_001138390.1:n.594+3_594+4delinsGA
NM_001144919.1:c.672+3_672+4delinsGA	NP_001138391.1:n.672+3_672+4delinsGA
NM_022970.3:c.939+3_939+4delinsGA	NP_075259.4:n.939+3_939+4delinsGA
NM_023029.2:c.672+3_672+4delinsGA	NP_075418.1:n.672+3_672+4delinsGA
NR_073009.1:n.1241+3_1241+4delinsGA
XM_006717708.2:c.996+3_996+4delinsGA	XP_006717771.1:n.996+3_996+4delinsGA
XM_006717709.2:c.996+3_996+4delinsGA	XP_006717772.1:n.996+3_996+4delinsGA
XM_006717710.2:c.996+3_996+4delinsGA	XP_006717773.1:n.996+3_996+4delinsGA
XM_006717711.2:c.729+3_729+4delinsGA	XP_006717774.1:n.729+3_729+4delinsGA
XM_006717712.2:c.651+3_651+4delinsGA	XP_006717775.1:n.651+3_651+4delinsGA
XM_006717713.2:c.996+3_996+4delinsGA	XP_006717776.1:n.996+3_996+4delinsGA
XM_011539510.1:c.255+3_255+4delinsGA	XP_011537812.1:n.255+3_255+4delinsGA
NM_001320654.1:c.255+3_255+4delinsGA	NP_001307583.1:n.255+3_255+4delinsGA
NM_001320658.1:c.939+3_939+4delinsGA	NP_001307587.1:n.939+3_939+4delinsGA
XM_006717708.3:c.996+3_996+4delinsGA	XP_006717771.1:n.996+3_996+4delinsGA
XM_006717710.4:c.996+3_996+4delinsGA	XP_006717773.1:n.996+3_996+4delinsGA
XM_017015920.2:c.996+3_996+4delinsGA	XP_016871409.1:n.996+3_996+4delinsGA
XM_017015921.2:c.996+3_996+4delinsGA	XP_016871410.1:n.996+3_996+4delinsGA
XM_017015924.2:c.651+3_651+4delinsGA	XP_016871413.1:n.651+3_651+4delinsGA
XM_017015925.2:c.651+3_651+4delinsGA	XP_016871414.1:n.651+3_651+4delinsGA
XM_024447887.1:c.729+3_729+4delinsGA	XP_024303655.1:n.729+3_729+4delinsGA
XM_024447888.1:c.729+3_729+4delinsGA	XP_024303656.1:n.729+3_729+4delinsGA
XM_024447889.1:c.729+3_729+4delinsGA	XP_024303657.1:n.729+3_729+4delinsGA
XM_024447890.1:c.729+3_729+4delinsGA	XP_024303658.1:n.729+3_729+4delinsGA
XM_024447891.1:c.651+3_651+4delinsGA	XP_024303659.1:n.651+3_651+4delinsGA
XM_024447892.1:c.-232+3_-232+4delinsGA	XP_024303660.1:n.-232+3_-232+4delinsGA
NM_000141.5:c.939+3_939+4delinsGA MANE Select	NP_000132.3:n.939+3_939+4delinsGA
NM_001144917.2:c.939+3_939+4delinsGA	NP_001138389.1:n.939+3_939+4delinsGA
NM_001144918.2:c.594+3_594+4delinsGA	NP_001138390.1:n.594+3_594+4delinsGA
NM_001144919.2:c.672+3_672+4delinsGA	NP_001138391.1:n.672+3_672+4delinsGA
NM_001320658.2:c.939+3_939+4delinsGA	NP_001307587.1:n.939+3_939+4delinsGA
NR_073009.2:n.1227+3_1227+4delinsGA
NM_001144915.2:c.672+3_672+4delinsGA	NP_001138387.1:n.672+3_672+4delinsGA
NM_001144916.2:c.594+3_594+4delinsGA	NP_001138388.1:n.594+3_594+4delinsGA
NM_001320654.2:c.255+3_255+4delinsGA	NP_001307583.1:n.255+3_255+4delinsGA