Canonical Allele Identifier: CA1941012793

Gene: FGFR2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121488155_121488156delinsAC , CM000672.2:g.121488155_121488156delinsAC	GRCh38
NC_000010.10:g.123247669_123247670delinsAC , CM000672.1:g.123247669_123247670delinsAC	GRCh37
NC_000010.9:g.123237659_123237660delinsAC	NCBI36
NG_012449.1:g.115303_115304delinsGT
NG_012449.2:g.115303_115304delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000457416.7:c.1867-43_1867-42delinsGT MANE Plus Clinical	ENSP00000410294.2:n.1867-43_1867-42delinsGT
ENST00000351936.11:c.1858-43_1858-42delinsGT	ENSP00000309878.10:n.1858-43_1858-42delinsGT
ENST00000638709.2:c.688-43_688-42delinsGT	ENSP00000491912.2:n.688-43_688-42delinsGT
ENST00000682296.1:n.1206-43_1206-42delinsGT
ENST00000682550.1:c.1513-43_1513-42delinsGT	ENSP00000507633.1:n.1513-43_1513-42delinsGT
ENST00000682772.1:c.688-43_688-42delinsGT	ENSP00000506848.1:n.688-43_688-42delinsGT
ENST00000682904.1:n.684-43_684-42delinsGT
ENST00000683029.1:n.276-43_276-42delinsGT
ENST00000683211.1:c.1858-43_1858-42delinsGT	ENSP00000508257.1:n.1858-43_1858-42delinsGT
ENST00000683250.1:c.*566-43_*566-42delinsGT	ENSP00000506847.1:n.*566-43_*566-42delinsGT
ENST00000683418.1:n.4205-43_4205-42delinsGT
ENST00000684153.1:c.1513-43_1513-42delinsGT	ENSP00000506937.1:n.1513-43_1513-42delinsGT
ENST00000684516.1:n.2877-43_2877-42delinsGT
ENST00000358487.10:c.1864-43_1864-42delinsGT MANE Select	ENSP00000351276.6:n.1864-43_1864-42delinsGT
ENST00000336553.10:c.1591-43_1591-42delinsGT	ENSP00000337665.6:n.1591-43_1591-42delinsGT
ENST00000346997.6:c.1858-43_1858-42delinsGT	ENSP00000263451.5:n.1858-43_1858-42delinsGT
ENST00000351936.10:c.1864-43_1864-42delinsGT	ENSP00000309878.9:n.1864-43_1864-42delinsGT
ENST00000356226.8:c.1513-43_1513-42delinsGT	ENSP00000348559.4:n.1513-43_1513-42delinsGT
ENST00000357555.9:c.1597-43_1597-42delinsGT	ENSP00000350166.5:n.1597-43_1597-42delinsGT
ENST00000358487.9:c.1864-43_1864-42delinsGT	ENSP00000351276.5:n.1864-43_1864-42delinsGT
ENST00000360144.7:c.1600-43_1600-42delinsGT	ENSP00000353262.3:n.1600-43_1600-42delinsGT
ENST00000369056.5:c.1867-43_1867-42delinsGT	ENSP00000358052.1:n.1867-43_1867-42delinsGT
ENST00000369058.7:c.1867-43_1867-42delinsGT	ENSP00000358054.3:n.1867-43_1867-42delinsGT
ENST00000369059.5:c.1522-43_1522-42delinsGT	ENSP00000358055.1:n.1522-43_1522-42delinsGT
ENST00000369060.8:c.1516-43_1516-42delinsGT	ENSP00000358056.4:n.1516-43_1516-42delinsGT
ENST00000369061.8:c.1528-43_1528-42delinsGT	ENSP00000358057.4:n.1528-43_1528-42delinsGT
ENST00000429361.5:c.640-43_640-42delinsGT	ENSP00000404219.1:n.640-43_640-42delinsGT
ENST00000457416.6:c.1867-43_1867-42delinsGT	ENSP00000410294.2:n.1867-43_1867-42delinsGT
ENST00000478859.5:c.1180-43_1180-42delinsGT	ENSP00000474011.1:n.1180-43_1180-42delinsGT
ENST00000604236.5:c.*911-43_*911-42delinsGT	ENSP00000474109.1:n.*911-43_*911-42delinsGT
ENST00000613048.4:c.1597-43_1597-42delinsGT	ENSP00000484154.1:n.1597-43_1597-42delinsGT
NM_000141.4:c.1864-43_1864-42delinsGT	NP_000132.3:n.1864-43_1864-42delinsGT
NM_001144913.1:c.1867-43_1867-42delinsGT	NP_001138385.1:n.1867-43_1867-42delinsGT
NM_001144914.1:c.1528-43_1528-42delinsGT	NP_001138386.1:n.1528-43_1528-42delinsGT
NM_001144915.1:c.1597-43_1597-42delinsGT	NP_001138387.1:n.1597-43_1597-42delinsGT
NM_001144916.1:c.1519-43_1519-42delinsGT	NP_001138388.1:n.1519-43_1519-42delinsGT
NM_001144917.1:c.1516-43_1516-42delinsGT	NP_001138389.1:n.1516-43_1516-42delinsGT
NM_001144918.1:c.1513-43_1513-42delinsGT	NP_001138390.1:n.1513-43_1513-42delinsGT
NM_001144919.1:c.1600-43_1600-42delinsGT	NP_001138391.1:n.1600-43_1600-42delinsGT
NM_022970.3:c.1867-43_1867-42delinsGT	NP_075259.4:n.1867-43_1867-42delinsGT
NM_023029.2:c.1597-43_1597-42delinsGT	NP_075418.1:n.1597-43_1597-42delinsGT
NR_073009.1:n.2314-43_2314-42delinsGT
XM_006717708.2:c.1918-43_1918-42delinsGT	XP_006717771.1:n.1918-43_1918-42delinsGT
XM_006717709.2:c.1915-43_1915-42delinsGT	XP_006717772.1:n.1915-43_1915-42delinsGT
XM_006717710.2:c.1924-43_1924-42delinsGT	XP_006717773.1:n.1924-43_1924-42delinsGT
XM_006717711.2:c.1657-43_1657-42delinsGT	XP_006717774.1:n.1657-43_1657-42delinsGT
XM_006717712.2:c.1579-43_1579-42delinsGT	XP_006717775.1:n.1579-43_1579-42delinsGT
XM_006717713.2:c.1921-43_1921-42delinsGT	XP_006717776.1:n.1921-43_1921-42delinsGT
XM_011539510.1:c.1180-43_1180-42delinsGT	XP_011537812.1:n.1180-43_1180-42delinsGT
NM_001320654.1:c.1180-43_1180-42delinsGT	NP_001307583.1:n.1180-43_1180-42delinsGT
NM_001320658.1:c.1858-43_1858-42delinsGT	NP_001307587.1:n.1858-43_1858-42delinsGT
XM_006717708.3:c.1918-43_1918-42delinsGT	XP_006717771.1:n.1918-43_1918-42delinsGT
XM_006717710.4:c.1924-43_1924-42delinsGT	XP_006717773.1:n.1924-43_1924-42delinsGT
XM_017015920.2:c.1918-43_1918-42delinsGT	XP_016871409.1:n.1918-43_1918-42delinsGT
XM_017015921.2:c.1915-43_1915-42delinsGT	XP_016871410.1:n.1915-43_1915-42delinsGT
XM_017015924.2:c.1576-43_1576-42delinsGT	XP_016871413.1:n.1576-43_1576-42delinsGT
XM_017015925.2:c.1570-43_1570-42delinsGT	XP_016871414.1:n.1570-43_1570-42delinsGT
XM_024447887.1:c.1654-43_1654-42delinsGT	XP_024303655.1:n.1654-43_1654-42delinsGT
XM_024447888.1:c.1651-43_1651-42delinsGT	XP_024303656.1:n.1651-43_1651-42delinsGT
XM_024447889.1:c.1648-43_1648-42delinsGT	XP_024303657.1:n.1648-43_1648-42delinsGT
XM_024447890.1:c.1657-43_1657-42delinsGT	XP_024303658.1:n.1657-43_1657-42delinsGT
XM_024447891.1:c.1579-43_1579-42delinsGT	XP_024303659.1:n.1579-43_1579-42delinsGT
XM_024447892.1:c.694-43_694-42delinsGT	XP_024303660.1:n.694-43_694-42delinsGT
NM_000141.5:c.1864-43_1864-42delinsGT MANE Select	NP_000132.3:n.1864-43_1864-42delinsGT
NM_001144917.2:c.1516-43_1516-42delinsGT	NP_001138389.1:n.1516-43_1516-42delinsGT
NM_001144918.2:c.1513-43_1513-42delinsGT	NP_001138390.1:n.1513-43_1513-42delinsGT
NM_001144919.2:c.1600-43_1600-42delinsGT	NP_001138391.1:n.1600-43_1600-42delinsGT
NM_001320658.2:c.1858-43_1858-42delinsGT	NP_001307587.1:n.1858-43_1858-42delinsGT
NR_073009.2:n.2300-43_2300-42delinsGT
NM_001144915.2:c.1597-43_1597-42delinsGT	NP_001138387.1:n.1597-43_1597-42delinsGT
NM_001144916.2:c.1519-43_1519-42delinsGT	NP_001138388.1:n.1519-43_1519-42delinsGT
NM_001320654.2:c.1180-43_1180-42delinsGT	NP_001307583.1:n.1180-43_1180-42delinsGT