Canonical Allele Identifier: CA2840366792
Gene: FGFR2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121479668_121479669insAGGAGGAGAAGAAGGT , CM000672.2:g.121479668_121479669insAGGAGGAGAAGAAGGT GRCh38
NC_000010.10:g.123239182_123239183insAGGAGGAGAAGAAGGT , CM000672.1:g.123239182_123239183insAGGAGGAGAAGAAGGT GRCh37
NC_000010.9:g.123229172_123229173insAGGAGGAGAAGAAGGT NCBI36
NG_012449.1:g.123790_123791insACCTTCTTCTCCTCCT
NG_012449.2:g.123790_123791insACCTTCTTCTCCTCCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000457416.7:c.*188_*189insACCTTCTTCTCCTCCT MANE Plus Clinical ENSP00000410294.2:n.*188_*189insACCTTCTTCTCCTCCT
ENST00000351936.11:c.*188_*189insACCTTCTTCTCCTCCT ENSP00000309878.10:n.*188_*189insACCTTCTTCTCCTCCT
ENST00000638709.2:c.*188_*189insACCTTCTTCTCCTCCT ENSP00000491912.2:n.*188_*189insACCTTCTTCTCCTCCT
ENST00000682296.1:n.1996_1997insACCTTCTTCTCCTCCT
ENST00000682550.1:c.*188_*189insACCTTCTTCTCCTCCT ENSP00000507633.1:n.*188_*189insACCTTCTTCTCCTCCT
ENST00000682772.1:c.*188_*189insACCTTCTTCTCCTCCT ENSP00000506848.1:n.*188_*189insACCTTCTTCTCCTCCT
ENST00000682904.1:n.1474_1475insACCTTCTTCTCCTCCT
ENST00000683029.1:n.2657_2658insACCTTCTTCTCCTCCT
ENST00000683211.1:c.*188_*189insACCTTCTTCTCCTCCT ENSP00000508257.1:n.*188_*189insACCTTCTTCTCCTCCT
ENST00000683250.1:c.*2947_*2948insACCTTCTTCTCCTCCT ENSP00000506847.1:n.*2947_*2948insACCTTCTTCTCCTCCT
ENST00000683418.1:n.4995_4996insACCTTCTTCTCCTCCT
ENST00000684153.1:c.*382_*383insACCTTCTTCTCCTCCT ENSP00000506937.1:n.*382_*383insACCTTCTTCTCCTCCT
ENST00000684516.1:n.3667_3668insACCTTCTTCTCCTCCT
ENST00000358487.10:c.*188_*189insACCTTCTTCTCCTCCT MANE Select ENSP00000351276.6:n.*188_*189insACCTTCTTCTCCTCCT
ENST00000638709.1:c.641_642insACCTTCTTCTCCTCCT
ENST00000356226.8:c.*188_*189insACCTTCTTCTCCTCCT ENSP00000348559.4:n.*188_*189insACCTTCTTCTCCTCCT
ENST00000357555.9:c.2036_2037insACCTTCTTCTCCTCCT ENSP00000350166.5:p.Glu680ProfsTer21
ENST00000358487.9:c.*188_*189insACCTTCTTCTCCTCCT ENSP00000351276.5:n.*188_*189insACCTTCTTCTCCTCCT
ENST00000369059.5:c.*188_*189insACCTTCTTCTCCTCCT ENSP00000358055.1:n.*188_*189insACCTTCTTCTCCTCCT
ENST00000369060.8:c.*188_*189insACCTTCTTCTCCTCCT ENSP00000358056.4:n.*188_*189insACCTTCTTCTCCTCCT
ENST00000369061.8:c.*188_*189insACCTTCTTCTCCTCCT ENSP00000358057.4:n.*188_*189insACCTTCTTCTCCTCCT
ENST00000478859.5:c.*188_*189insACCTTCTTCTCCTCCT ENSP00000474011.1:n.*188_*189insACCTTCTTCTCCTCCT
ENST00000604236.5:c.*1701_*1702insACCTTCTTCTCCTCCT ENSP00000474109.1:n.*1701_*1702insACCTTCTTCTCCTCCT
ENST00000613048.4:c.*188_*189insACCTTCTTCTCCTCCT ENSP00000484154.1:n.*188_*189insACCTTCTTCTCCTCCT
NM_000141.4:c.*188_*189insACCTTCTTCTCCTCCT NP_000132.3:n.*188_*189insACCTTCTTCTCCTCCT
NM_001144914.1:c.*188_*189insACCTTCTTCTCCTCCT NP_001138386.1:n.*188_*189insACCTTCTTCTCCTCCT
NM_001144915.1:c.2036_2037insACCTTCTTCTCCTCCT NP_001138387.1:p.Glu680ProfsTer21
NM_001144916.1:c.*188_*189insACCTTCTTCTCCTCCT NP_001138388.1:n.*188_*189insACCTTCTTCTCCTCCT
NM_001144917.1:c.*188_*189insACCTTCTTCTCCTCCT NP_001138389.1:n.*188_*189insACCTTCTTCTCCTCCT
NM_001144918.1:c.*188_*189insACCTTCTTCTCCTCCT NP_001138390.1:n.*188_*189insACCTTCTTCTCCTCCT
NM_022970.3:c.*188_*189insACCTTCTTCTCCTCCT NP_075259.4:n.*188_*189insACCTTCTTCTCCTCCT
NM_023029.2:c.*188_*189insACCTTCTTCTCCTCCT NP_075418.1:n.*188_*189insACCTTCTTCTCCTCCT
NR_073009.1:n.3104_3105insACCTTCTTCTCCTCCT
XM_006717708.2:c.*188_*189insACCTTCTTCTCCTCCT XP_006717771.1:n.*188_*189insACCTTCTTCTCCTCCT
XM_006717709.2:c.*188_*189insACCTTCTTCTCCTCCT XP_006717772.1:n.*188_*189insACCTTCTTCTCCTCCT
XM_006717711.2:c.*188_*189insACCTTCTTCTCCTCCT XP_006717774.1:n.*188_*189insACCTTCTTCTCCTCCT
XM_006717712.2:c.*188_*189insACCTTCTTCTCCTCCT XP_006717775.1:n.*188_*189insACCTTCTTCTCCTCCT
XM_011539510.1:c.*188_*189insACCTTCTTCTCCTCCT XP_011537812.1:n.*188_*189insACCTTCTTCTCCTCCT
NM_001320654.1:c.*188_*189insACCTTCTTCTCCTCCT NP_001307583.1:n.*188_*189insACCTTCTTCTCCTCCT
NM_001320658.1:c.*188_*189insACCTTCTTCTCCTCCT NP_001307587.1:n.*188_*189insACCTTCTTCTCCTCCT
XM_006717708.3:c.*188_*189insACCTTCTTCTCCTCCT XP_006717771.1:n.*188_*189insACCTTCTTCTCCTCCT
XM_006717710.4:c.*382_*383insACCTTCTTCTCCTCCT XP_006717773.1:n.*382_*383insACCTTCTTCTCCTCCT
XM_017015920.2:c.*382_*383insACCTTCTTCTCCTCCT XP_016871409.1:n.*382_*383insACCTTCTTCTCCTCCT
XM_017015921.2:c.*382_*383insACCTTCTTCTCCTCCT XP_016871410.1:n.*382_*383insACCTTCTTCTCCTCCT
XM_017015924.2:c.*188_*189insACCTTCTTCTCCTCCT XP_016871413.1:n.*188_*189insACCTTCTTCTCCTCCT
XM_017015925.2:c.*382_*383insACCTTCTTCTCCTCCT XP_016871414.1:n.*382_*383insACCTTCTTCTCCTCCT
XM_024447887.1:c.*188_*189insACCTTCTTCTCCTCCT XP_024303655.1:n.*188_*189insACCTTCTTCTCCTCCT
XM_024447888.1:c.*188_*189insACCTTCTTCTCCTCCT XP_024303656.1:n.*188_*189insACCTTCTTCTCCTCCT
XM_024447889.1:c.*188_*189insACCTTCTTCTCCTCCT XP_024303657.1:n.*188_*189insACCTTCTTCTCCTCCT
XM_024447890.1:c.*188_*189insACCTTCTTCTCCTCCT XP_024303658.1:n.*188_*189insACCTTCTTCTCCTCCT
XM_024447891.1:c.*188_*189insACCTTCTTCTCCTCCT XP_024303659.1:n.*188_*189insACCTTCTTCTCCTCCT
XM_024447892.1:c.*188_*189insACCTTCTTCTCCTCCT XP_024303660.1:n.*188_*189insACCTTCTTCTCCTCCT
NM_000141.5:c.*188_*189insACCTTCTTCTCCTCCT MANE Select NP_000132.3:n.*188_*189insACCTTCTTCTCCTCCT
NM_001144917.2:c.*188_*189insACCTTCTTCTCCTCCT NP_001138389.1:n.*188_*189insACCTTCTTCTCCTCCT
NM_001144918.2:c.*188_*189insACCTTCTTCTCCTCCT NP_001138390.1:n.*188_*189insACCTTCTTCTCCTCCT
NM_001320658.2:c.*188_*189insACCTTCTTCTCCTCCT NP_001307587.1:n.*188_*189insACCTTCTTCTCCTCCT
NR_073009.2:n.3090_3091insACCTTCTTCTCCTCCT
NM_001144915.2:c.2036_2037insACCTTCTTCTCCTCCT NP_001138387.1:p.Glu680ProfsTer21
NM_001144916.2:c.*188_*189insACCTTCTTCTCCTCCT NP_001138388.1:n.*188_*189insACCTTCTTCTCCTCCT
NM_001320654.2:c.*188_*189insACCTTCTTCTCCTCCT NP_001307583.1:n.*188_*189insACCTTCTTCTCCTCCT
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