Canonical Allele Identifier: CA2611201005
Gene: FGFR2 HGNC NCBI

Linked Data

gnomAD v4: 10-121488251-TAC-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121488253_121488254del , CM000672.2:g.121488253_121488254del GRCh38
NC_000010.10:g.123247767_123247768del , CM000672.1:g.123247767_123247768del GRCh37
NC_000010.9:g.123237757_123237758del NCBI36
NG_012449.1:g.115206_115207del
NG_012449.2:g.115206_115207del

Transcript Alleles

HGVS Amino-acid Change
ENST00000457416.7:c.1867-140_1867-139del MANE Plus Clinical ENSP00000410294.2:n.1867-140_1867-139del
ENST00000351936.11:c.1858-140_1858-139del ENSP00000309878.10:n.1858-140_1858-139del
ENST00000638709.2:c.688-140_688-139del ENSP00000491912.2:n.688-140_688-139del
ENST00000682296.1:n.1206-140_1206-139del
ENST00000682550.1:c.1513-140_1513-139del ENSP00000507633.1:n.1513-140_1513-139del
ENST00000682772.1:c.688-140_688-139del ENSP00000506848.1:n.688-140_688-139del
ENST00000682904.1:n.684-140_684-139del
ENST00000683029.1:n.276-140_276-139del
ENST00000683211.1:c.1858-140_1858-139del ENSP00000508257.1:n.1858-140_1858-139del
ENST00000683250.1:c.*566-140_*566-139del ENSP00000506847.1:n.*566-140_*566-139del
ENST00000683418.1:n.4205-140_4205-139del
ENST00000684153.1:c.1513-140_1513-139del ENSP00000506937.1:n.1513-140_1513-139del
ENST00000684516.1:n.2877-140_2877-139del
ENST00000358487.10:c.1864-140_1864-139del MANE Select ENSP00000351276.6:n.1864-140_1864-139del
ENST00000336553.10:c.1591-140_1591-139del ENSP00000337665.6:n.1591-140_1591-139del
ENST00000346997.6:c.1858-140_1858-139del ENSP00000263451.5:n.1858-140_1858-139del
ENST00000351936.10:c.1864-140_1864-139del ENSP00000309878.9:n.1864-140_1864-139del
ENST00000356226.8:c.1513-140_1513-139del ENSP00000348559.4:n.1513-140_1513-139del
ENST00000357555.9:c.1597-140_1597-139del ENSP00000350166.5:n.1597-140_1597-139del
ENST00000358487.9:c.1864-140_1864-139del ENSP00000351276.5:n.1864-140_1864-139del
ENST00000360144.7:c.1600-140_1600-139del ENSP00000353262.3:n.1600-140_1600-139del
ENST00000369056.5:c.1867-140_1867-139del ENSP00000358052.1:n.1867-140_1867-139del
ENST00000369058.7:c.1867-140_1867-139del ENSP00000358054.3:n.1867-140_1867-139del
ENST00000369059.5:c.1522-140_1522-139del ENSP00000358055.1:n.1522-140_1522-139del
ENST00000369060.8:c.1516-140_1516-139del ENSP00000358056.4:n.1516-140_1516-139del
ENST00000369061.8:c.1528-140_1528-139del ENSP00000358057.4:n.1528-140_1528-139del
ENST00000429361.5:c.640-140_640-139del ENSP00000404219.1:n.640-140_640-139del
ENST00000457416.6:c.1867-140_1867-139del ENSP00000410294.2:n.1867-140_1867-139del
ENST00000478859.5:c.1180-140_1180-139del ENSP00000474011.1:n.1180-140_1180-139del
ENST00000604236.5:c.*911-140_*911-139del ENSP00000474109.1:n.*911-140_*911-139del
ENST00000613048.4:c.1597-140_1597-139del ENSP00000484154.1:n.1597-140_1597-139del
NM_000141.4:c.1864-140_1864-139del NP_000132.3:n.1864-140_1864-139del
NM_001144913.1:c.1867-140_1867-139del NP_001138385.1:n.1867-140_1867-139del
NM_001144914.1:c.1528-140_1528-139del NP_001138386.1:n.1528-140_1528-139del
NM_001144915.1:c.1597-140_1597-139del NP_001138387.1:n.1597-140_1597-139del
NM_001144916.1:c.1519-140_1519-139del NP_001138388.1:n.1519-140_1519-139del
NM_001144917.1:c.1516-140_1516-139del NP_001138389.1:n.1516-140_1516-139del
NM_001144918.1:c.1513-140_1513-139del NP_001138390.1:n.1513-140_1513-139del
NM_001144919.1:c.1600-140_1600-139del NP_001138391.1:n.1600-140_1600-139del
NM_022970.3:c.1867-140_1867-139del NP_075259.4:n.1867-140_1867-139del
NM_023029.2:c.1597-140_1597-139del NP_075418.1:n.1597-140_1597-139del
NR_073009.1:n.2314-140_2314-139del
XM_006717708.2:c.1918-140_1918-139del XP_006717771.1:n.1918-140_1918-139del
XM_006717709.2:c.1915-140_1915-139del XP_006717772.1:n.1915-140_1915-139del
XM_006717710.2:c.1924-140_1924-139del XP_006717773.1:n.1924-140_1924-139del
XM_006717711.2:c.1657-140_1657-139del XP_006717774.1:n.1657-140_1657-139del
XM_006717712.2:c.1579-140_1579-139del XP_006717775.1:n.1579-140_1579-139del
XM_006717713.2:c.1921-140_1921-139del XP_006717776.1:n.1921-140_1921-139del
XM_011539510.1:c.1180-140_1180-139del XP_011537812.1:n.1180-140_1180-139del
NM_001320654.1:c.1180-140_1180-139del NP_001307583.1:n.1180-140_1180-139del
NM_001320658.1:c.1858-140_1858-139del NP_001307587.1:n.1858-140_1858-139del
XM_006717708.3:c.1918-140_1918-139del XP_006717771.1:n.1918-140_1918-139del
XM_006717710.4:c.1924-140_1924-139del XP_006717773.1:n.1924-140_1924-139del
XM_017015920.2:c.1918-140_1918-139del XP_016871409.1:n.1918-140_1918-139del
XM_017015921.2:c.1915-140_1915-139del XP_016871410.1:n.1915-140_1915-139del
XM_017015924.2:c.1576-140_1576-139del XP_016871413.1:n.1576-140_1576-139del
XM_017015925.2:c.1570-140_1570-139del XP_016871414.1:n.1570-140_1570-139del
XM_024447887.1:c.1654-140_1654-139del XP_024303655.1:n.1654-140_1654-139del
XM_024447888.1:c.1651-140_1651-139del XP_024303656.1:n.1651-140_1651-139del
XM_024447889.1:c.1648-140_1648-139del XP_024303657.1:n.1648-140_1648-139del
XM_024447890.1:c.1657-140_1657-139del XP_024303658.1:n.1657-140_1657-139del
XM_024447891.1:c.1579-140_1579-139del XP_024303659.1:n.1579-140_1579-139del
XM_024447892.1:c.694-140_694-139del XP_024303660.1:n.694-140_694-139del
NM_000141.5:c.1864-140_1864-139del MANE Select NP_000132.3:n.1864-140_1864-139del
NM_001144917.2:c.1516-140_1516-139del NP_001138389.1:n.1516-140_1516-139del
NM_001144918.2:c.1513-140_1513-139del NP_001138390.1:n.1513-140_1513-139del
NM_001144919.2:c.1600-140_1600-139del NP_001138391.1:n.1600-140_1600-139del
NM_001320658.2:c.1858-140_1858-139del NP_001307587.1:n.1858-140_1858-139del
NR_073009.2:n.2300-140_2300-139del
NM_001144915.2:c.1597-140_1597-139del NP_001138387.1:n.1597-140_1597-139del
NM_001144916.2:c.1519-140_1519-139del NP_001138388.1:n.1519-140_1519-139del
NM_001320654.2:c.1180-140_1180-139del NP_001307583.1:n.1180-140_1180-139del
Search 100 bp 5'
Search 100 bp 3'