Canonical Allele Identifier: CA2789751619

Gene: FGFR2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121488166_121488167insAAAA , CM000672.2:g.121488166_121488167insAAAA	GRCh38
NC_000010.10:g.123247680_123247681insAAAA , CM000672.1:g.123247680_123247681insAAAA	GRCh37
NC_000010.9:g.123237670_123237671insAAAA	NCBI36
NG_012449.1:g.115294_115295insTTTT
NG_012449.2:g.115294_115295insTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000457416.7:c.1867-52_1867-51insTTTT MANE Plus Clinical	ENSP00000410294.2:n.1867-52_1867-51insTTTT
ENST00000351936.11:c.1858-52_1858-51insTTTT	ENSP00000309878.10:n.1858-52_1858-51insTTTT
ENST00000638709.2:c.688-52_688-51insTTTT	ENSP00000491912.2:n.688-52_688-51insTTTT
ENST00000682296.1:n.1206-52_1206-51insTTTT
ENST00000682550.1:c.1513-52_1513-51insTTTT	ENSP00000507633.1:n.1513-52_1513-51insTTTT
ENST00000682772.1:c.688-52_688-51insTTTT	ENSP00000506848.1:n.688-52_688-51insTTTT
ENST00000682904.1:n.684-52_684-51insTTTT
ENST00000683029.1:n.276-52_276-51insTTTT
ENST00000683211.1:c.1858-52_1858-51insTTTT	ENSP00000508257.1:n.1858-52_1858-51insTTTT
ENST00000683250.1:c.*566-52_*566-51insTTTT	ENSP00000506847.1:n.*566-52_*566-51insTTTT
ENST00000683418.1:n.4205-52_4205-51insTTTT
ENST00000684153.1:c.1513-52_1513-51insTTTT	ENSP00000506937.1:n.1513-52_1513-51insTTTT
ENST00000684516.1:n.2877-52_2877-51insTTTT
ENST00000358487.10:c.1864-52_1864-51insTTTT MANE Select	ENSP00000351276.6:n.1864-52_1864-51insTTTT
ENST00000336553.10:c.1591-52_1591-51insTTTT	ENSP00000337665.6:n.1591-52_1591-51insTTTT
ENST00000346997.6:c.1858-52_1858-51insTTTT	ENSP00000263451.5:n.1858-52_1858-51insTTTT
ENST00000351936.10:c.1864-52_1864-51insTTTT	ENSP00000309878.9:n.1864-52_1864-51insTTTT
ENST00000356226.8:c.1513-52_1513-51insTTTT	ENSP00000348559.4:n.1513-52_1513-51insTTTT
ENST00000357555.9:c.1597-52_1597-51insTTTT	ENSP00000350166.5:n.1597-52_1597-51insTTTT
ENST00000358487.9:c.1864-52_1864-51insTTTT	ENSP00000351276.5:n.1864-52_1864-51insTTTT
ENST00000360144.7:c.1600-52_1600-51insTTTT	ENSP00000353262.3:n.1600-52_1600-51insTTTT
ENST00000369056.5:c.1867-52_1867-51insTTTT	ENSP00000358052.1:n.1867-52_1867-51insTTTT
ENST00000369058.7:c.1867-52_1867-51insTTTT	ENSP00000358054.3:n.1867-52_1867-51insTTTT
ENST00000369059.5:c.1522-52_1522-51insTTTT	ENSP00000358055.1:n.1522-52_1522-51insTTTT
ENST00000369060.8:c.1516-52_1516-51insTTTT	ENSP00000358056.4:n.1516-52_1516-51insTTTT
ENST00000369061.8:c.1528-52_1528-51insTTTT	ENSP00000358057.4:n.1528-52_1528-51insTTTT
ENST00000429361.5:c.640-52_640-51insTTTT	ENSP00000404219.1:n.640-52_640-51insTTTT
ENST00000457416.6:c.1867-52_1867-51insTTTT	ENSP00000410294.2:n.1867-52_1867-51insTTTT
ENST00000478859.5:c.1180-52_1180-51insTTTT	ENSP00000474011.1:n.1180-52_1180-51insTTTT
ENST00000604236.5:c.*911-52_*911-51insTTTT	ENSP00000474109.1:n.*911-52_*911-51insTTTT
ENST00000613048.4:c.1597-52_1597-51insTTTT	ENSP00000484154.1:n.1597-52_1597-51insTTTT
NM_000141.4:c.1864-52_1864-51insTTTT	NP_000132.3:n.1864-52_1864-51insTTTT
NM_001144913.1:c.1867-52_1867-51insTTTT	NP_001138385.1:n.1867-52_1867-51insTTTT
NM_001144914.1:c.1528-52_1528-51insTTTT	NP_001138386.1:n.1528-52_1528-51insTTTT
NM_001144915.1:c.1597-52_1597-51insTTTT	NP_001138387.1:n.1597-52_1597-51insTTTT
NM_001144916.1:c.1519-52_1519-51insTTTT	NP_001138388.1:n.1519-52_1519-51insTTTT
NM_001144917.1:c.1516-52_1516-51insTTTT	NP_001138389.1:n.1516-52_1516-51insTTTT
NM_001144918.1:c.1513-52_1513-51insTTTT	NP_001138390.1:n.1513-52_1513-51insTTTT
NM_001144919.1:c.1600-52_1600-51insTTTT	NP_001138391.1:n.1600-52_1600-51insTTTT
NM_022970.3:c.1867-52_1867-51insTTTT	NP_075259.4:n.1867-52_1867-51insTTTT
NM_023029.2:c.1597-52_1597-51insTTTT	NP_075418.1:n.1597-52_1597-51insTTTT
NR_073009.1:n.2314-52_2314-51insTTTT
XM_006717708.2:c.1918-52_1918-51insTTTT	XP_006717771.1:n.1918-52_1918-51insTTTT
XM_006717709.2:c.1915-52_1915-51insTTTT	XP_006717772.1:n.1915-52_1915-51insTTTT
XM_006717710.2:c.1924-52_1924-51insTTTT	XP_006717773.1:n.1924-52_1924-51insTTTT
XM_006717711.2:c.1657-52_1657-51insTTTT	XP_006717774.1:n.1657-52_1657-51insTTTT
XM_006717712.2:c.1579-52_1579-51insTTTT	XP_006717775.1:n.1579-52_1579-51insTTTT
XM_006717713.2:c.1921-52_1921-51insTTTT	XP_006717776.1:n.1921-52_1921-51insTTTT
XM_011539510.1:c.1180-52_1180-51insTTTT	XP_011537812.1:n.1180-52_1180-51insTTTT
NM_001320654.1:c.1180-52_1180-51insTTTT	NP_001307583.1:n.1180-52_1180-51insTTTT
NM_001320658.1:c.1858-52_1858-51insTTTT	NP_001307587.1:n.1858-52_1858-51insTTTT
XM_006717708.3:c.1918-52_1918-51insTTTT	XP_006717771.1:n.1918-52_1918-51insTTTT
XM_006717710.4:c.1924-52_1924-51insTTTT	XP_006717773.1:n.1924-52_1924-51insTTTT
XM_017015920.2:c.1918-52_1918-51insTTTT	XP_016871409.1:n.1918-52_1918-51insTTTT
XM_017015921.2:c.1915-52_1915-51insTTTT	XP_016871410.1:n.1915-52_1915-51insTTTT
XM_017015924.2:c.1576-52_1576-51insTTTT	XP_016871413.1:n.1576-52_1576-51insTTTT
XM_017015925.2:c.1570-52_1570-51insTTTT	XP_016871414.1:n.1570-52_1570-51insTTTT
XM_024447887.1:c.1654-52_1654-51insTTTT	XP_024303655.1:n.1654-52_1654-51insTTTT
XM_024447888.1:c.1651-52_1651-51insTTTT	XP_024303656.1:n.1651-52_1651-51insTTTT
XM_024447889.1:c.1648-52_1648-51insTTTT	XP_024303657.1:n.1648-52_1648-51insTTTT
XM_024447890.1:c.1657-52_1657-51insTTTT	XP_024303658.1:n.1657-52_1657-51insTTTT
XM_024447891.1:c.1579-52_1579-51insTTTT	XP_024303659.1:n.1579-52_1579-51insTTTT
XM_024447892.1:c.694-52_694-51insTTTT	XP_024303660.1:n.694-52_694-51insTTTT
NM_000141.5:c.1864-52_1864-51insTTTT MANE Select	NP_000132.3:n.1864-52_1864-51insTTTT
NM_001144917.2:c.1516-52_1516-51insTTTT	NP_001138389.1:n.1516-52_1516-51insTTTT
NM_001144918.2:c.1513-52_1513-51insTTTT	NP_001138390.1:n.1513-52_1513-51insTTTT
NM_001144919.2:c.1600-52_1600-51insTTTT	NP_001138391.1:n.1600-52_1600-51insTTTT
NM_001320658.2:c.1858-52_1858-51insTTTT	NP_001307587.1:n.1858-52_1858-51insTTTT
NR_073009.2:n.2300-52_2300-51insTTTT
NM_001144915.2:c.1597-52_1597-51insTTTT	NP_001138387.1:n.1597-52_1597-51insTTTT
NM_001144916.2:c.1519-52_1519-51insTTTT	NP_001138388.1:n.1519-52_1519-51insTTTT
NM_001320654.2:c.1180-52_1180-51insTTTT	NP_001307583.1:n.1180-52_1180-51insTTTT