Canonical Allele Identifier: CA918777578
Gene: FGFR2 HGNC NCBI

Linked Data

dbSNP Id: rs1564719876
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121574549_121574550insTA , CM000672.2:g.121574549_121574550insTA GRCh38
NC_000010.10:g.123334063_123334064insTA , CM000672.1:g.123334063_123334064insTA GRCh37
NC_000010.9:g.123324053_123324054insTA NCBI36
NG_012449.1:g.28909_28910insTA
NG_012449.2:g.28909_28910insTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000457416.7:c.110-8846_110-8845insTA MANE Plus Clinical ENSP00000410294.2:n.110-8846_110-8845insTA
ENST00000351936.11:c.110-8846_110-8845insTA ENSP00000309878.10:n.110-8846_110-8845insTA
ENST00000682400.1:n.109+19159_109+19160insTA
ENST00000682550.1:c.109+19159_109+19160insTA ENSP00000507633.1:n.109+19159_109+19160insTA
ENST00000683035.1:c.110-8846_110-8845insTA ENSP00000507074.1:n.110-8846_110-8845insTA
ENST00000683211.1:c.110-8846_110-8845insTA ENSP00000508257.1:n.110-8846_110-8845insTA
ENST00000683250.1:c.109+19159_109+19160insTA ENSP00000506847.1:n.109+19159_109+19160insTA
ENST00000683678.1:n.110-8846_110-8845insTA
ENST00000684153.1:c.109+19159_109+19160insTA ENSP00000506937.1:n.109+19159_109+19160insTA
ENST00000358487.10:c.110-8846_110-8845insTA MANE Select ENSP00000351276.6:n.110-8846_110-8845insTA
ENST00000636922.1:c.110-8846_110-8845insTA ENSP00000490905.1:n.110-8846_110-8845insTA
ENST00000336553.10:c.110-9971_110-9970insTA ENSP00000337665.6:n.110-9971_110-9970insTA
ENST00000346997.6:c.110-8846_110-8845insTA ENSP00000263451.5:n.110-8846_110-8845insTA
ENST00000351936.10:c.110-8846_110-8845insTA ENSP00000309878.9:n.110-8846_110-8845insTA
ENST00000356226.8:c.109+19159_109+19160insTA ENSP00000348559.4:n.109+19159_109+19160insTA
ENST00000357555.9:c.110-9971_110-9970insTA ENSP00000350166.5:n.110-9971_110-9970insTA
ENST00000358487.9:c.110-8846_110-8845insTA ENSP00000351276.5:n.110-8846_110-8845insTA
ENST00000359354.6:c.110-8846_110-8845insTA ENSP00000352309.2:n.110-8846_110-8845insTA
ENST00000360144.7:c.110-9971_110-9970insTA ENSP00000353262.3:n.110-9971_110-9970insTA
ENST00000369056.5:c.110-8846_110-8845insTA ENSP00000358052.1:n.110-8846_110-8845insTA
ENST00000369058.7:c.110-8846_110-8845insTA ENSP00000358054.3:n.110-8846_110-8845insTA
ENST00000369059.5:c.109+19159_109+19160insTA ENSP00000358055.1:n.109+19159_109+19160insTA
ENST00000369060.8:c.110-8846_110-8845insTA ENSP00000358056.4:n.110-8846_110-8845insTA
ENST00000369061.8:c.110-8846_110-8845insTA ENSP00000358057.4:n.110-8846_110-8845insTA
ENST00000457416.6:c.110-8846_110-8845insTA ENSP00000410294.2:n.110-8846_110-8845insTA
ENST00000490349.5:n.371-8846_371-8845insTA
ENST00000604236.5:c.109+19159_109+19160insTA ENSP00000474109.1:n.109+19159_109+19160insTA
ENST00000611527.1:c.110-9971_110-9970insTA ENSP00000484892.1:n.110-9971_110-9970insTA
ENST00000613048.4:c.110-9971_110-9970insTA ENSP00000484154.1:n.110-9971_110-9970insTA
ENST00000613324.4:c.57-8846_57-8845insTA
NM_000141.4:c.110-8846_110-8845insTA NP_000132.3:n.110-8846_110-8845insTA
NM_001144913.1:c.110-8846_110-8845insTA NP_001138385.1:n.110-8846_110-8845insTA
NM_001144914.1:c.110-8846_110-8845insTA NP_001138386.1:n.110-8846_110-8845insTA
NM_001144915.1:c.110-9971_110-9970insTA NP_001138387.1:n.110-9971_110-9970insTA
NM_001144916.1:c.109+19159_109+19160insTA NP_001138388.1:n.109+19159_109+19160insTA
NM_001144917.1:c.110-8846_110-8845insTA NP_001138389.1:n.110-8846_110-8845insTA
NM_001144918.1:c.109+19159_109+19160insTA NP_001138390.1:n.109+19159_109+19160insTA
NM_001144919.1:c.110-9971_110-9970insTA NP_001138391.1:n.110-9971_110-9970insTA
NM_022970.3:c.110-8846_110-8845insTA NP_075259.4:n.110-8846_110-8845insTA
NM_023029.2:c.110-9971_110-9970insTA NP_075418.1:n.110-9971_110-9970insTA
NR_073009.1:n.756+19159_756+19160insTA
XM_006717708.2:c.167-8846_167-8845insTA XP_006717771.1:n.167-8846_167-8845insTA
XM_006717709.2:c.167-8846_167-8845insTA XP_006717772.1:n.167-8846_167-8845insTA
XM_006717710.2:c.167-8846_167-8845insTA XP_006717773.1:n.167-8846_167-8845insTA
XM_006717711.2:c.167-9971_167-9970insTA XP_006717774.1:n.167-9971_167-9970insTA
XM_006717712.2:c.166+19159_166+19160insTA XP_006717775.1:n.166+19159_166+19160insTA
XM_006717713.2:c.167-8846_167-8845insTA XP_006717776.1:n.167-8846_167-8845insTA
NM_001320658.1:c.110-8846_110-8845insTA NP_001307587.1:n.110-8846_110-8845insTA
XM_006717708.3:c.167-8846_167-8845insTA XP_006717771.1:n.167-8846_167-8845insTA
XM_006717710.4:c.167-8846_167-8845insTA XP_006717773.1:n.167-8846_167-8845insTA
XM_017015920.2:c.167-8846_167-8845insTA XP_016871409.1:n.167-8846_167-8845insTA
XM_017015921.2:c.167-8846_167-8845insTA XP_016871410.1:n.167-8846_167-8845insTA
XM_017015924.2:c.166+19159_166+19160insTA XP_016871413.1:n.166+19159_166+19160insTA
XM_017015925.2:c.166+19159_166+19160insTA XP_016871414.1:n.166+19159_166+19160insTA
XM_024447887.1:c.167-9971_167-9970insTA XP_024303655.1:n.167-9971_167-9970insTA
XM_024447888.1:c.167-9971_167-9970insTA XP_024303656.1:n.167-9971_167-9970insTA
XM_024447889.1:c.167-9971_167-9970insTA XP_024303657.1:n.167-9971_167-9970insTA
XM_024447890.1:c.167-9971_167-9970insTA XP_024303658.1:n.167-9971_167-9970insTA
XM_024447891.1:c.166+19159_166+19160insTA XP_024303659.1:n.166+19159_166+19160insTA
NM_000141.5:c.110-8846_110-8845insTA MANE Select NP_000132.3:n.110-8846_110-8845insTA
NM_001144917.2:c.110-8846_110-8845insTA NP_001138389.1:n.110-8846_110-8845insTA
NM_001144918.2:c.109+19159_109+19160insTA NP_001138390.1:n.109+19159_109+19160insTA
NM_001144919.2:c.110-9971_110-9970insTA NP_001138391.1:n.110-9971_110-9970insTA
NM_001320658.2:c.110-8846_110-8845insTA NP_001307587.1:n.110-8846_110-8845insTA
NR_073009.2:n.742+19159_742+19160insTA
NM_001144915.2:c.110-9971_110-9970insTA NP_001138387.1:n.110-9971_110-9970insTA
NM_001144916.2:c.109+19159_109+19160insTA NP_001138388.1:n.109+19159_109+19160insTA
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