Canonical Allele Identifier: CA2789751623
Gene: FGFR2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121488266_121488267del , CM000672.2:g.121488266_121488267del GRCh38
NC_000010.10:g.123247780_123247781del , CM000672.1:g.123247780_123247781del GRCh37
NC_000010.9:g.123237770_123237771del NCBI36
NG_012449.1:g.115193_115194del
NG_012449.2:g.115193_115194del

Transcript Alleles

HGVS Amino-acid Change
ENST00000457416.7:c.1867-153_1867-152del MANE Plus Clinical ENSP00000410294.2:n.1867-153_1867-152del
ENST00000351936.11:c.1858-153_1858-152del ENSP00000309878.10:n.1858-153_1858-152del
ENST00000638709.2:c.688-153_688-152del ENSP00000491912.2:n.688-153_688-152del
ENST00000682296.1:n.1206-153_1206-152del
ENST00000682550.1:c.1513-153_1513-152del ENSP00000507633.1:n.1513-153_1513-152del
ENST00000682772.1:c.688-153_688-152del ENSP00000506848.1:n.688-153_688-152del
ENST00000682904.1:n.684-153_684-152del
ENST00000683029.1:n.276-153_276-152del
ENST00000683211.1:c.1858-153_1858-152del ENSP00000508257.1:n.1858-153_1858-152del
ENST00000683250.1:c.*566-153_*566-152del ENSP00000506847.1:n.*566-153_*566-152del
ENST00000683418.1:n.4205-153_4205-152del
ENST00000684153.1:c.1513-153_1513-152del ENSP00000506937.1:n.1513-153_1513-152del
ENST00000684516.1:n.2877-153_2877-152del
ENST00000358487.10:c.1864-153_1864-152del MANE Select ENSP00000351276.6:n.1864-153_1864-152del
ENST00000336553.10:c.1591-153_1591-152del ENSP00000337665.6:n.1591-153_1591-152del
ENST00000346997.6:c.1858-153_1858-152del ENSP00000263451.5:n.1858-153_1858-152del
ENST00000351936.10:c.1864-153_1864-152del ENSP00000309878.9:n.1864-153_1864-152del
ENST00000356226.8:c.1513-153_1513-152del ENSP00000348559.4:n.1513-153_1513-152del
ENST00000357555.9:c.1597-153_1597-152del ENSP00000350166.5:n.1597-153_1597-152del
ENST00000358487.9:c.1864-153_1864-152del ENSP00000351276.5:n.1864-153_1864-152del
ENST00000360144.7:c.1600-153_1600-152del ENSP00000353262.3:n.1600-153_1600-152del
ENST00000369056.5:c.1867-153_1867-152del ENSP00000358052.1:n.1867-153_1867-152del
ENST00000369058.7:c.1867-153_1867-152del ENSP00000358054.3:n.1867-153_1867-152del
ENST00000369059.5:c.1522-153_1522-152del ENSP00000358055.1:n.1522-153_1522-152del
ENST00000369060.8:c.1516-153_1516-152del ENSP00000358056.4:n.1516-153_1516-152del
ENST00000369061.8:c.1528-153_1528-152del ENSP00000358057.4:n.1528-153_1528-152del
ENST00000429361.5:c.640-153_640-152del ENSP00000404219.1:n.640-153_640-152del
ENST00000457416.6:c.1867-153_1867-152del ENSP00000410294.2:n.1867-153_1867-152del
ENST00000478859.5:c.1180-153_1180-152del ENSP00000474011.1:n.1180-153_1180-152del
ENST00000604236.5:c.*911-153_*911-152del ENSP00000474109.1:n.*911-153_*911-152del
ENST00000613048.4:c.1597-153_1597-152del ENSP00000484154.1:n.1597-153_1597-152del
NM_000141.4:c.1864-153_1864-152del NP_000132.3:n.1864-153_1864-152del
NM_001144913.1:c.1867-153_1867-152del NP_001138385.1:n.1867-153_1867-152del
NM_001144914.1:c.1528-153_1528-152del NP_001138386.1:n.1528-153_1528-152del
NM_001144915.1:c.1597-153_1597-152del NP_001138387.1:n.1597-153_1597-152del
NM_001144916.1:c.1519-153_1519-152del NP_001138388.1:n.1519-153_1519-152del
NM_001144917.1:c.1516-153_1516-152del NP_001138389.1:n.1516-153_1516-152del
NM_001144918.1:c.1513-153_1513-152del NP_001138390.1:n.1513-153_1513-152del
NM_001144919.1:c.1600-153_1600-152del NP_001138391.1:n.1600-153_1600-152del
NM_022970.3:c.1867-153_1867-152del NP_075259.4:n.1867-153_1867-152del
NM_023029.2:c.1597-153_1597-152del NP_075418.1:n.1597-153_1597-152del
NR_073009.1:n.2314-153_2314-152del
XM_006717708.2:c.1918-153_1918-152del XP_006717771.1:n.1918-153_1918-152del
XM_006717709.2:c.1915-153_1915-152del XP_006717772.1:n.1915-153_1915-152del
XM_006717710.2:c.1924-153_1924-152del XP_006717773.1:n.1924-153_1924-152del
XM_006717711.2:c.1657-153_1657-152del XP_006717774.1:n.1657-153_1657-152del
XM_006717712.2:c.1579-153_1579-152del XP_006717775.1:n.1579-153_1579-152del
XM_006717713.2:c.1921-153_1921-152del XP_006717776.1:n.1921-153_1921-152del
XM_011539510.1:c.1180-153_1180-152del XP_011537812.1:n.1180-153_1180-152del
NM_001320654.1:c.1180-153_1180-152del NP_001307583.1:n.1180-153_1180-152del
NM_001320658.1:c.1858-153_1858-152del NP_001307587.1:n.1858-153_1858-152del
XM_006717708.3:c.1918-153_1918-152del XP_006717771.1:n.1918-153_1918-152del
XM_006717710.4:c.1924-153_1924-152del XP_006717773.1:n.1924-153_1924-152del
XM_017015920.2:c.1918-153_1918-152del XP_016871409.1:n.1918-153_1918-152del
XM_017015921.2:c.1915-153_1915-152del XP_016871410.1:n.1915-153_1915-152del
XM_017015924.2:c.1576-153_1576-152del XP_016871413.1:n.1576-153_1576-152del
XM_017015925.2:c.1570-153_1570-152del XP_016871414.1:n.1570-153_1570-152del
XM_024447887.1:c.1654-153_1654-152del XP_024303655.1:n.1654-153_1654-152del
XM_024447888.1:c.1651-153_1651-152del XP_024303656.1:n.1651-153_1651-152del
XM_024447889.1:c.1648-153_1648-152del XP_024303657.1:n.1648-153_1648-152del
XM_024447890.1:c.1657-153_1657-152del XP_024303658.1:n.1657-153_1657-152del
XM_024447891.1:c.1579-153_1579-152del XP_024303659.1:n.1579-153_1579-152del
XM_024447892.1:c.694-153_694-152del XP_024303660.1:n.694-153_694-152del
NM_000141.5:c.1864-153_1864-152del MANE Select NP_000132.3:n.1864-153_1864-152del
NM_001144917.2:c.1516-153_1516-152del NP_001138389.1:n.1516-153_1516-152del
NM_001144918.2:c.1513-153_1513-152del NP_001138390.1:n.1513-153_1513-152del
NM_001144919.2:c.1600-153_1600-152del NP_001138391.1:n.1600-153_1600-152del
NM_001320658.2:c.1858-153_1858-152del NP_001307587.1:n.1858-153_1858-152del
NR_073009.2:n.2300-153_2300-152del
NM_001144915.2:c.1597-153_1597-152del NP_001138387.1:n.1597-153_1597-152del
NM_001144916.2:c.1519-153_1519-152del NP_001138388.1:n.1519-153_1519-152del
NM_001320654.2:c.1180-153_1180-152del NP_001307583.1:n.1180-153_1180-152del
Search 100 bp 5'
Search 100 bp 3'