Canonical Allele Identifier: CA2722988890
Gene: FGFR2 HGNC NCBI

Linked Data

dbSNP Id: rs2134262174
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121517499_121517501del , CM000672.2:g.121517499_121517501del GRCh38
NC_000010.10:g.123277013_123277015del , CM000672.1:g.123277013_123277015del GRCh37
NC_000010.9:g.123267003_123267005del NCBI36
NG_012449.1:g.85961_85963del
NG_012449.2:g.85961_85963del

Transcript Alleles

HGVS Amino-acid Change
ENST00000457416.7:c.1087+1184_1087+1186del MANE Plus Clinical ENSP00000410294.2:n.1087+1184_1087+1186del
ENST00000351936.11:c.940-35_940-33del ENSP00000309878.10:n.940-35_940-33del
ENST00000638709.2:c.-231-35_-231-33del ENSP00000491912.2:n.-231-35_-231-33del
ENST00000682296.1:n.288-35_288-33del
ENST00000682400.1:n.595-35_595-33del
ENST00000682550.1:c.595-35_595-33del ENSP00000507633.1:n.595-35_595-33del
ENST00000682772.1:c.-231-35_-231-33del ENSP00000506848.1:n.-231-35_-231-33del
ENST00000683211.1:c.940-35_940-33del ENSP00000508257.1:n.940-35_940-33del
ENST00000683250.1:c.404-13557_404-13555del ENSP00000506847.1:n.404-13557_404-13555del
ENST00000683418.1:n.3287-35_3287-33del
ENST00000683678.1:n.940-35_940-33del
ENST00000684153.1:c.595-35_595-33del ENSP00000506937.1:n.595-35_595-33del
ENST00000358487.10:c.940-35_940-33del MANE Select ENSP00000351276.6:n.940-35_940-33del
ENST00000336553.10:c.673-35_673-33del ENSP00000337665.6:n.673-35_673-33del
ENST00000346997.6:c.940-35_940-33del ENSP00000263451.5:n.940-35_940-33del
ENST00000351936.10:c.940-26_940-24del ENSP00000309878.9:n.940-26_940-24del
ENST00000356226.8:c.595-35_595-33del ENSP00000348559.4:n.595-35_595-33del
ENST00000357555.9:c.673-35_673-33del ENSP00000350166.5:n.673-35_673-33del
ENST00000358487.9:c.940-35_940-33del ENSP00000351276.5:n.940-35_940-33del
ENST00000360144.7:c.820+1184_820+1186del ENSP00000353262.3:n.820+1184_820+1186del
ENST00000369056.5:c.1087+1184_1087+1186del ENSP00000358052.1:n.1087+1184_1087+1186del
ENST00000369058.7:c.1087+1184_1087+1186del ENSP00000358054.3:n.1087+1184_1087+1186del
ENST00000369059.5:c.742+1184_742+1186del ENSP00000358055.1:n.742+1184_742+1186del
ENST00000369060.8:c.939+2481_939+2483del ENSP00000358056.4:n.939+2481_939+2483del
ENST00000369061.8:c.749-2179_749-2177del ENSP00000358057.4:n.749-2179_749-2177del
ENST00000457416.6:c.1087+1184_1087+1186del ENSP00000410294.2:n.1087+1184_1087+1186del
ENST00000463870.5:n.149-35_149-33del
ENST00000478859.5:c.256-35_256-33del ENSP00000474011.1:n.256-35_256-33del
ENST00000490349.5:n.1349-35_1349-33del
ENST00000604236.5:c.743-35_743-33del ENSP00000474109.1:n.743-35_743-33del
ENST00000613048.4:c.673-35_673-33del ENSP00000484154.1:n.673-35_673-33del
NM_000141.4:c.940-35_940-33del NP_000132.3:n.940-35_940-33del
NM_001144913.1:c.1087+1184_1087+1186del NP_001138385.1:n.1087+1184_1087+1186del
NM_001144914.1:c.749-2179_749-2177del NP_001138386.1:n.749-2179_749-2177del
NM_001144915.1:c.673-35_673-33del NP_001138387.1:n.673-35_673-33del
NM_001144916.1:c.595-35_595-33del NP_001138388.1:n.595-35_595-33del
NM_001144917.1:c.939+2481_939+2483del NP_001138389.1:n.939+2481_939+2483del
NM_001144918.1:c.595-35_595-33del NP_001138390.1:n.595-35_595-33del
NM_001144919.1:c.820+1184_820+1186del NP_001138391.1:n.820+1184_820+1186del
NM_022970.3:c.1087+1184_1087+1186del NP_075259.4:n.1087+1184_1087+1186del
NM_023029.2:c.673-35_673-33del NP_075418.1:n.673-35_673-33del
NR_073009.1:n.1390-35_1390-33del
XM_006717708.2:c.1144+1184_1144+1186del XP_006717771.1:n.1144+1184_1144+1186del
XM_006717709.2:c.997-35_997-33del XP_006717772.1:n.997-35_997-33del
XM_006717710.2:c.1144+1184_1144+1186del XP_006717773.1:n.1144+1184_1144+1186del
XM_006717711.2:c.877+1184_877+1186del XP_006717774.1:n.877+1184_877+1186del
XM_006717712.2:c.799+1184_799+1186del XP_006717775.1:n.799+1184_799+1186del
XM_006717713.2:c.997-35_997-33del XP_006717776.1:n.997-35_997-33del
XM_011539510.1:c.256-35_256-33del XP_011537812.1:n.256-35_256-33del
NM_001320654.1:c.256-35_256-33del NP_001307583.1:n.256-35_256-33del
NM_001320658.1:c.940-35_940-33del NP_001307587.1:n.940-35_940-33del
XM_006717708.3:c.1144+1184_1144+1186del XP_006717771.1:n.1144+1184_1144+1186del
XM_006717710.4:c.1144+1184_1144+1186del XP_006717773.1:n.1144+1184_1144+1186del
XM_017015920.2:c.1144+1184_1144+1186del XP_016871409.1:n.1144+1184_1144+1186del
XM_017015921.2:c.997-35_997-33del XP_016871410.1:n.997-35_997-33del
XM_017015924.2:c.652-35_652-33del XP_016871413.1:n.652-35_652-33del
XM_017015925.2:c.652-35_652-33del XP_016871414.1:n.652-35_652-33del
XM_024447887.1:c.730-35_730-33del XP_024303655.1:n.730-35_730-33del
XM_024447888.1:c.877+1184_877+1186del XP_024303656.1:n.877+1184_877+1186del
XM_024447889.1:c.730-35_730-33del XP_024303657.1:n.730-35_730-33del
XM_024447890.1:c.877+1184_877+1186del XP_024303658.1:n.877+1184_877+1186del
XM_024447891.1:c.799+1184_799+1186del XP_024303659.1:n.799+1184_799+1186del
XM_024447892.1:c.-231-35_-231-33del XP_024303660.1:n.-231-35_-231-33del
NM_000141.5:c.940-35_940-33del MANE Select NP_000132.3:n.940-35_940-33del
NM_001144917.2:c.939+2481_939+2483del NP_001138389.1:n.939+2481_939+2483del
NM_001144918.2:c.595-35_595-33del NP_001138390.1:n.595-35_595-33del
NM_001144919.2:c.820+1184_820+1186del NP_001138391.1:n.820+1184_820+1186del
NM_001320658.2:c.940-35_940-33del NP_001307587.1:n.940-35_940-33del
NR_073009.2:n.1376-35_1376-33del
NM_001144915.2:c.673-35_673-33del NP_001138387.1:n.673-35_673-33del
NM_001144916.2:c.595-35_595-33del NP_001138388.1:n.595-35_595-33del
NM_001320654.2:c.256-35_256-33del NP_001307583.1:n.256-35_256-33del
Search 100 bp 5'
Search 100 bp 3'