Canonical Allele Identifier: CA2611201061

Gene: FGFR2

Linked Data

• gnomAD v4: 10-121520020-T-TTCC

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121520020_121520021insTCC , CM000672.2:g.121520020_121520021insTCC	GRCh38
NC_000010.10:g.123279534_123279535insTCC , CM000672.1:g.123279534_123279535insTCC	GRCh37
NC_000010.9:g.123269524_123269525insTCC	NCBI36
NG_012449.1:g.83438_83439insGGA
NG_012449.2:g.83438_83439insGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000457416.7:c.897_898insGGA MANE Plus Clinical	ENSP00000410294.2:p.Ser299_Lys300insGly
ENST00000351936.11:c.897_898insGGA	ENSP00000309878.10:p.Ser299_Lys300insGly
ENST00000638709.2:c.-274_-273insGGA	ENSP00000491912.2:n.-274_-273insGGA
ENST00000682296.1:n.245_246insGGA
ENST00000682400.1:n.552_553insGGA
ENST00000682550.1:c.552_553insGGA	ENSP00000507633.1:p.Ser184_Lys185insGly
ENST00000682772.1:c.-274_-273insGGA	ENSP00000506848.1:n.-274_-273insGGA
ENST00000683211.1:c.897_898insGGA	ENSP00000508257.1:p.Ser299_Lys300insGly
ENST00000683250.1:c.404-16080_404-16079insGGA	ENSP00000506847.1:n.404-16080_404-16079insGGA
ENST00000683418.1:n.3244_3245insGGA
ENST00000683678.1:n.897_898insGGA
ENST00000684153.1:c.552_553insGGA	ENSP00000506937.1:p.Ser184_Lys185insGly
ENST00000358487.10:c.897_898insGGA MANE Select	ENSP00000351276.6:p.Ser299_Lys300insGly
ENST00000336553.10:c.630_631insGGA	ENSP00000337665.6:p.Ser210_Lys211insGly
ENST00000346997.6:c.897_898insGGA	ENSP00000263451.5:p.Ser299_Lys300insGly
ENST00000351936.10:c.897_898insGGA	ENSP00000309878.9:p.Ser299_Lys300insGly
ENST00000356226.8:c.552_553insGGA	ENSP00000348559.4:p.Ser184_Lys185insGly
ENST00000357555.9:c.630_631insGGA	ENSP00000350166.5:p.Ser210_Lys211insGly
ENST00000358487.9:c.897_898insGGA	ENSP00000351276.5:p.Ser299_Lys300insGly
ENST00000360144.7:c.630_631insGGA	ENSP00000353262.3:p.Ser210_Lys211insGly
ENST00000369056.5:c.897_898insGGA	ENSP00000358052.1:p.Ser299_Lys300insGly
ENST00000369058.7:c.897_898insGGA	ENSP00000358054.3:p.Ser299_Lys300insGly
ENST00000369059.5:c.552_553insGGA	ENSP00000358055.1:p.Ser184_Lys185insGly
ENST00000369060.8:c.897_898insGGA	ENSP00000358056.4:p.Ser299_Lys300insGly
ENST00000369061.8:c.749-4702_749-4701insGGA	ENSP00000358057.4:n.749-4702_749-4701insGGA
ENST00000457416.6:c.897_898insGGA	ENSP00000410294.2:p.Ser299_Lys300insGly
ENST00000478859.5:c.213_214insGGA	ENSP00000474011.1:p.Ser71_Lys72insGly
ENST00000490349.5:n.1158_1159insGGA
ENST00000604236.5:c.552_553insGGA	ENSP00000474109.1:p.Ser184_Lys185insGly
ENST00000613048.4:c.630_631insGGA	ENSP00000484154.1:p.Ser210_Lys211insGly
NM_000141.4:c.897_898insGGA	NP_000132.3:p.Ser299_Lys300insGly
NM_001144913.1:c.897_898insGGA	NP_001138385.1:p.Ser299_Lys300insGly
NM_001144914.1:c.749-4702_749-4701insGGA	NP_001138386.1:n.749-4702_749-4701insGGA
NM_001144915.1:c.630_631insGGA	NP_001138387.1:p.Ser210_Lys211insGly
NM_001144916.1:c.552_553insGGA	NP_001138388.1:p.Ser184_Lys185insGly
NM_001144917.1:c.897_898insGGA	NP_001138389.1:p.Ser299_Lys300insGly
NM_001144918.1:c.552_553insGGA	NP_001138390.1:p.Ser184_Lys185insGly
NM_001144919.1:c.630_631insGGA	NP_001138391.1:p.Ser210_Lys211insGly
NM_022970.3:c.897_898insGGA	NP_075259.4:p.Ser299_Lys300insGly
NM_023029.2:c.630_631insGGA	NP_075418.1:p.Ser210_Lys211insGly
NR_073009.1:n.1199_1200insGGA
XM_006717708.2:c.954_955insGGA	XP_006717771.1:p.Ser318_Lys319insGly
XM_006717709.2:c.954_955insGGA	XP_006717772.1:p.Ser318_Lys319insGly
XM_006717710.2:c.954_955insGGA	XP_006717773.1:p.Ser318_Lys319insGly
XM_006717711.2:c.687_688insGGA	XP_006717774.1:p.Ser229_Lys230insGly
XM_006717712.2:c.609_610insGGA	XP_006717775.1:p.Ser203_Lys204insGly
XM_006717713.2:c.954_955insGGA	XP_006717776.1:p.Ser318_Lys319insGly
XM_011539510.1:c.213_214insGGA	XP_011537812.1:p.Ser71_Lys72insGly
NM_001320654.1:c.213_214insGGA	NP_001307583.1:p.Ser71_Lys72insGly
NM_001320658.1:c.897_898insGGA	NP_001307587.1:p.Ser299_Lys300insGly
XM_006717708.3:c.954_955insGGA	XP_006717771.1:p.Ser318_Lys319insGly
XM_006717710.4:c.954_955insGGA	XP_006717773.1:p.Ser318_Lys319insGly
XM_017015920.2:c.954_955insGGA	XP_016871409.1:p.Ser318_Lys319insGly
XM_017015921.2:c.954_955insGGA	XP_016871410.1:p.Ser318_Lys319insGly
XM_017015924.2:c.609_610insGGA	XP_016871413.1:p.Ser203_Lys204insGly
XM_017015925.2:c.609_610insGGA	XP_016871414.1:p.Ser203_Lys204insGly
XM_024447887.1:c.687_688insGGA	XP_024303655.1:p.Ser229_Lys230insGly
XM_024447888.1:c.687_688insGGA	XP_024303656.1:p.Ser229_Lys230insGly
XM_024447889.1:c.687_688insGGA	XP_024303657.1:p.Ser229_Lys230insGly
XM_024447890.1:c.687_688insGGA	XP_024303658.1:p.Ser229_Lys230insGly
XM_024447891.1:c.609_610insGGA	XP_024303659.1:p.Ser203_Lys204insGly
XM_024447892.1:c.-274_-273insGGA	XP_024303660.1:n.-274_-273insGGA
NM_000141.5:c.897_898insGGA MANE Select	NP_000132.3:p.Ser299_Lys300insGly
NM_001144917.2:c.897_898insGGA	NP_001138389.1:p.Ser299_Lys300insGly
NM_001144918.2:c.552_553insGGA	NP_001138390.1:p.Ser184_Lys185insGly
NM_001144919.2:c.630_631insGGA	NP_001138391.1:p.Ser210_Lys211insGly
NM_001320658.2:c.897_898insGGA	NP_001307587.1:p.Ser299_Lys300insGly
NR_073009.2:n.1185_1186insGGA
NM_001144915.2:c.630_631insGGA	NP_001138387.1:p.Ser210_Lys211insGly
NM_001144916.2:c.552_553insGGA	NP_001138388.1:p.Ser184_Lys185insGly
NM_001320654.2:c.213_214insGGA	NP_001307583.1:p.Ser71_Lys72insGly