Canonical Allele Identifier: CA2695212876
Gene: FGFR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121517392_121517397dup , CM000672.2:g.121517392_121517397dup GRCh38
NC_000010.10:g.123276906_123276911dup , CM000672.1:g.123276906_123276911dup GRCh37
NC_000010.9:g.123266896_123266901dup NCBI36
NG_012449.1:g.86063_86068dup
NG_012449.2:g.86063_86068dup

Transcript Alleles

HGVS Amino-acid change
ENST00000457416.7:c.1087+1286_1087+1291dup MANE Plus Clinical ENSP00000410294.2:n.1087+1286_1087+1291du...
ENST00000351936.11:c.1007_1012dup ENSP00000309878.10:p.Ala337_Gly338insAspA...
ENST00000638709.2:c.-164_-159dup ENSP00000491912.2:n.-164_-159dup
ENST00000682296.1:n.355_360dup
ENST00000682400.1:n.662_667dup
ENST00000682550.1:c.662_667dup ENSP00000507633.1:p.Ala222_Gly223insAspAl...
ENST00000682772.1:c.-164_-159dup ENSP00000506848.1:n.-164_-159dup
ENST00000683211.1:c.1007_1012dup ENSP00000508257.1:p.Ala337_Gly338insAspAl...
ENST00000683250.1:c.404-13455_404-13450dup ENSP00000506847.1:n.404-13455_404-13450du...
ENST00000683418.1:n.3354_3359dup
ENST00000683678.1:n.1007_1012dup
ENST00000684153.1:c.662_667dup ENSP00000506937.1:p.Ala222_Gly223insAspAl...
ENST00000358487.10:c.1007_1012dup MANE Select ENSP00000351276.6:p.Ala337_Gly338insAspAl...
ENST00000336553.10:c.740_745dup ENSP00000337665.6:p.Ala248_Gly249insAspAl...
ENST00000346997.6:c.1007_1012dup ENSP00000263451.5:p.Ala337_Gly338insAspAl...
ENST00000351936.10:c.1013_1018dup ENSP00000309878.9:p.Ala339_Gly340insAspAl...
ENST00000356226.8:c.662_667dup ENSP00000348559.4:p.Ala222_Gly223insAspAl...
ENST00000357555.9:c.740_745dup ENSP00000350166.5:p.Ala248_Gly249insAspAl...
ENST00000358487.9:c.1007_1012dup ENSP00000351276.5:p.Ala337_Gly338insAspAl...
ENST00000360144.7:c.820+1286_820+1291dup ENSP00000353262.3:n.820+1286_820+1291dup
ENST00000369056.5:c.1087+1286_1087+1291dup ENSP00000358052.1:n.1087+1286_1087+1291du...
ENST00000369058.7:c.1087+1286_1087+1291dup ENSP00000358054.3:n.1087+1286_1087+1291du...
ENST00000369059.5:c.742+1286_742+1291dup ENSP00000358055.1:n.742+1286_742+1291dup
ENST00000369060.8:c.939+2583_939+2588dup ENSP00000358056.4:n.939+2583_939+2588dup
ENST00000369061.8:c.749-2077_749-2072dup ENSP00000358057.4:n.749-2077_749-2072dup
ENST00000457416.6:c.1087+1286_1087+1291dup ENSP00000410294.2:n.1087+1286_1087+1291du...
ENST00000463870.5:n.216_221dup
ENST00000478859.5:c.323_328dup ENSP00000474011.1:p.Ala109_Gly110insAspAl...
ENST00000490349.5:n.1416_1421dup
ENST00000604236.5:c.*54_*59dup ENSP00000474109.1:n.*54_*59dup
ENST00000613048.4:c.740_745dup ENSP00000484154.1:p.Ala248_Gly249insAspAl...
NM_000141.4:c.1007_1012dup NP_000132.3:p.Ala337_Gly338insAspAla
NM_001144913.1:c.1087+1286_1087+1291dup NP_001138385.1:n.1087+1286_1087+1291dup
NM_001144914.1:c.749-2077_749-2072dup NP_001138386.1:n.749-2077_749-2072dup
NM_001144915.1:c.740_745dup NP_001138387.1:p.Ala248_Gly249insAspAla
NM_001144916.1:c.662_667dup NP_001138388.1:p.Ala222_Gly223insAspAla
NM_001144917.1:c.939+2583_939+2588dup NP_001138389.1:n.939+2583_939+2588dup
NM_001144918.1:c.662_667dup NP_001138390.1:p.Ala222_Gly223insAspAla
NM_001144919.1:c.820+1286_820+1291dup NP_001138391.1:n.820+1286_820+1291dup
NM_022970.3:c.1087+1286_1087+1291dup NP_075259.4:n.1087+1286_1087+1291dup
NM_023029.2:c.740_745dup NP_075418.1:p.Ala248_Gly249insAspAla
NR_073009.1:n.1457_1462dup
XM_006717708.2:c.1144+1286_1144+1291dup XP_006717771.1:n.1144+1286_1144+1291dup
XM_006717709.2:c.1064_1069dup XP_006717772.1:p.Ala356_Gly357insAspAla
XM_006717710.2:c.1144+1286_1144+1291dup XP_006717773.1:n.1144+1286_1144+1291dup
XM_006717711.2:c.877+1286_877+1291dup XP_006717774.1:n.877+1286_877+1291dup
XM_006717712.2:c.799+1286_799+1291dup XP_006717775.1:n.799+1286_799+1291dup
XM_006717713.2:c.1064_1069dup XP_006717776.1:p.Ala356_Gly357insAspAla
XM_011539510.1:c.323_328dup XP_011537812.1:p.Ala109_Gly110insAspAla
NM_001320654.1:c.323_328dup NP_001307583.1:p.Ala109_Gly110insAspAla
NM_001320658.1:c.1007_1012dup NP_001307587.1:p.Ala337_Gly338insAspAla
XM_006717708.3:c.1144+1286_1144+1291dup XP_006717771.1:n.1144+1286_1144+1291dup
XM_006717710.4:c.1144+1286_1144+1291dup XP_006717773.1:n.1144+1286_1144+1291dup
XM_017015920.2:c.1144+1286_1144+1291dup XP_016871409.1:n.1144+1286_1144+1291dup
XM_017015921.2:c.1064_1069dup XP_016871410.1:p.Ala356_Gly357insAspAla
XM_017015924.2:c.719_724dup XP_016871413.1:p.Ala241_Gly242insAspAla
XM_017015925.2:c.719_724dup XP_016871414.1:p.Ala241_Gly242insAspAla
XM_024447887.1:c.797_802dup XP_024303655.1:p.Ala267_Gly268insAspAla
XM_024447888.1:c.877+1286_877+1291dup XP_024303656.1:n.877+1286_877+1291dup
XM_024447889.1:c.797_802dup XP_024303657.1:p.Ala267_Gly268insAspAla
XM_024447890.1:c.877+1286_877+1291dup XP_024303658.1:n.877+1286_877+1291dup
XM_024447891.1:c.799+1286_799+1291dup XP_024303659.1:n.799+1286_799+1291dup
XM_024447892.1:c.-164_-159dup XP_024303660.1:n.-164_-159dup
NM_000141.5:c.1007_1012dup MANE Select NP_000132.3:p.Ala337_Gly338insAspAla
NM_001144917.2:c.939+2583_939+2588dup NP_001138389.1:n.939+2583_939+2588dup
NM_001144918.2:c.662_667dup NP_001138390.1:p.Ala222_Gly223insAspAla
NM_001144919.2:c.820+1286_820+1291dup NP_001138391.1:n.820+1286_820+1291dup
NM_001320658.2:c.1007_1012dup NP_001307587.1:p.Ala337_Gly338insAspAla
NR_073009.2:n.1443_1448dup
NM_001144915.2:c.740_745dup NP_001138387.1:p.Ala248_Gly249insAspAla
NM_001144916.2:c.662_667dup NP_001138388.1:p.Ala222_Gly223insAspAla
NM_001320654.2:c.323_328dup NP_001307583.1:p.Ala109_Gly110insAspAla