Canonical Allele Identifier: CA2611200852
Gene: FGFR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121488144_121488147del , CM000672.2:g.121488144_121488147del GRCh38
NC_000010.10:g.123247658_123247661del , CM000672.1:g.123247658_123247661del GRCh37
NC_000010.9:g.123237648_123237651del NCBI36
NG_012449.1:g.115315_115318del
NG_012449.2:g.115315_115318del

Transcript Alleles

HGVS Amino-acid Change
ENST00000457416.7:c.1867-31_1867-28del MANE Plus Clinical ENSP00000410294.2:n.1867-31_1867-28del
ENST00000351936.11:c.1858-31_1858-28del ENSP00000309878.10:n.1858-31_1858-28del
ENST00000638709.2:c.688-31_688-28del ENSP00000491912.2:n.688-31_688-28del
ENST00000682296.1:n.1206-31_1206-28del
ENST00000682550.1:c.1513-31_1513-28del ENSP00000507633.1:n.1513-31_1513-28del
ENST00000682772.1:c.688-31_688-28del ENSP00000506848.1:n.688-31_688-28del
ENST00000682904.1:n.684-31_684-28del
ENST00000683029.1:n.276-31_276-28del
ENST00000683211.1:c.1858-31_1858-28del ENSP00000508257.1:n.1858-31_1858-28del
ENST00000683250.1:c.*566-31_*566-28del ENSP00000506847.1:n.*566-31_*566-28del
ENST00000683418.1:n.4205-31_4205-28del
ENST00000684153.1:c.1513-31_1513-28del ENSP00000506937.1:n.1513-31_1513-28del
ENST00000684516.1:n.2877-31_2877-28del
ENST00000358487.10:c.1864-31_1864-28del MANE Select ENSP00000351276.6:n.1864-31_1864-28del
ENST00000336553.10:c.1591-31_1591-28del ENSP00000337665.6:n.1591-31_1591-28del
ENST00000346997.6:c.1858-31_1858-28del ENSP00000263451.5:n.1858-31_1858-28del
ENST00000351936.10:c.1864-31_1864-28del ENSP00000309878.9:n.1864-31_1864-28del
ENST00000356226.8:c.1513-31_1513-28del ENSP00000348559.4:n.1513-31_1513-28del
ENST00000357555.9:c.1597-31_1597-28del ENSP00000350166.5:n.1597-31_1597-28del
ENST00000358487.9:c.1864-31_1864-28del ENSP00000351276.5:n.1864-31_1864-28del
ENST00000360144.7:c.1600-31_1600-28del ENSP00000353262.3:n.1600-31_1600-28del
ENST00000369056.5:c.1867-31_1867-28del ENSP00000358052.1:n.1867-31_1867-28del
ENST00000369058.7:c.1867-31_1867-28del ENSP00000358054.3:n.1867-31_1867-28del
ENST00000369059.5:c.1522-31_1522-28del ENSP00000358055.1:n.1522-31_1522-28del
ENST00000369060.8:c.1516-31_1516-28del ENSP00000358056.4:n.1516-31_1516-28del
ENST00000369061.8:c.1528-31_1528-28del ENSP00000358057.4:n.1528-31_1528-28del
ENST00000429361.5:c.640-31_640-28del ENSP00000404219.1:n.640-31_640-28del
ENST00000457416.6:c.1867-31_1867-28del ENSP00000410294.2:n.1867-31_1867-28del
ENST00000478859.5:c.1180-31_1180-28del ENSP00000474011.1:n.1180-31_1180-28del
ENST00000604236.5:c.*911-31_*911-28del ENSP00000474109.1:n.*911-31_*911-28del
ENST00000613048.4:c.1597-31_1597-28del ENSP00000484154.1:n.1597-31_1597-28del
NM_000141.4:c.1864-31_1864-28del NP_000132.3:n.1864-31_1864-28del
NM_001144913.1:c.1867-31_1867-28del NP_001138385.1:n.1867-31_1867-28del
NM_001144914.1:c.1528-31_1528-28del NP_001138386.1:n.1528-31_1528-28del
NM_001144915.1:c.1597-31_1597-28del NP_001138387.1:n.1597-31_1597-28del
NM_001144916.1:c.1519-31_1519-28del NP_001138388.1:n.1519-31_1519-28del
NM_001144917.1:c.1516-31_1516-28del NP_001138389.1:n.1516-31_1516-28del
NM_001144918.1:c.1513-31_1513-28del NP_001138390.1:n.1513-31_1513-28del
NM_001144919.1:c.1600-31_1600-28del NP_001138391.1:n.1600-31_1600-28del
NM_022970.3:c.1867-31_1867-28del NP_075259.4:n.1867-31_1867-28del
NM_023029.2:c.1597-31_1597-28del NP_075418.1:n.1597-31_1597-28del
NR_073009.1:n.2314-31_2314-28del
XM_006717708.2:c.1918-31_1918-28del XP_006717771.1:n.1918-31_1918-28del
XM_006717709.2:c.1915-31_1915-28del XP_006717772.1:n.1915-31_1915-28del
XM_006717710.2:c.1924-31_1924-28del XP_006717773.1:n.1924-31_1924-28del
XM_006717711.2:c.1657-31_1657-28del XP_006717774.1:n.1657-31_1657-28del
XM_006717712.2:c.1579-31_1579-28del XP_006717775.1:n.1579-31_1579-28del
XM_006717713.2:c.1921-31_1921-28del XP_006717776.1:n.1921-31_1921-28del
XM_011539510.1:c.1180-31_1180-28del XP_011537812.1:n.1180-31_1180-28del
NM_001320654.1:c.1180-31_1180-28del NP_001307583.1:n.1180-31_1180-28del
NM_001320658.1:c.1858-31_1858-28del NP_001307587.1:n.1858-31_1858-28del
XM_006717708.3:c.1918-31_1918-28del XP_006717771.1:n.1918-31_1918-28del
XM_006717710.4:c.1924-31_1924-28del XP_006717773.1:n.1924-31_1924-28del
XM_017015920.2:c.1918-31_1918-28del XP_016871409.1:n.1918-31_1918-28del
XM_017015921.2:c.1915-31_1915-28del XP_016871410.1:n.1915-31_1915-28del
XM_017015924.2:c.1576-31_1576-28del XP_016871413.1:n.1576-31_1576-28del
XM_017015925.2:c.1570-31_1570-28del XP_016871414.1:n.1570-31_1570-28del
XM_024447887.1:c.1654-31_1654-28del XP_024303655.1:n.1654-31_1654-28del
XM_024447888.1:c.1651-31_1651-28del XP_024303656.1:n.1651-31_1651-28del
XM_024447889.1:c.1648-31_1648-28del XP_024303657.1:n.1648-31_1648-28del
XM_024447890.1:c.1657-31_1657-28del XP_024303658.1:n.1657-31_1657-28del
XM_024447891.1:c.1579-31_1579-28del XP_024303659.1:n.1579-31_1579-28del
XM_024447892.1:c.694-31_694-28del XP_024303660.1:n.694-31_694-28del
NM_000141.5:c.1864-31_1864-28del MANE Select NP_000132.3:n.1864-31_1864-28del
NM_001144917.2:c.1516-31_1516-28del NP_001138389.1:n.1516-31_1516-28del
NM_001144918.2:c.1513-31_1513-28del NP_001138390.1:n.1513-31_1513-28del
NM_001144919.2:c.1600-31_1600-28del NP_001138391.1:n.1600-31_1600-28del
NM_001320658.2:c.1858-31_1858-28del NP_001307587.1:n.1858-31_1858-28del
NR_073009.2:n.2300-31_2300-28del
NM_001144915.2:c.1597-31_1597-28del NP_001138387.1:n.1597-31_1597-28del
NM_001144916.2:c.1519-31_1519-28del NP_001138388.1:n.1519-31_1519-28del
NM_001320654.2:c.1180-31_1180-28del NP_001307583.1:n.1180-31_1180-28del