Canonical Allele Identifier: CA2695212874
Gene: FGFR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121517363_121517410del , CM000672.2:g.121517363_121517410del GRCh38
NC_000010.10:g.123276877_123276924del , CM000672.1:g.123276877_123276924del GRCh37
NC_000010.9:g.123266867_123266914del NCBI36
NG_012449.1:g.86050_86097del
NG_012449.2:g.86050_86097del

Transcript Alleles

HGVS Amino-acid change
ENST00000457416.7:c.1087+1273_1087+1320del MANE Plus Clinical ENSP00000410294.2:n.1087+1273_1087+1320de...
ENST00000351936.11:c.994_1041del ENSP00000309878.10:p.Val332_Ser347del
ENST00000638709.2:c.-177_-130del ENSP00000491912.2:n.-177_-130del
ENST00000682296.1:n.342_389del
ENST00000682400.1:n.649_696del
ENST00000682550.1:c.649_696del ENSP00000507633.1:p.Val217_Ser232del
ENST00000682772.1:c.-177_-130del ENSP00000506848.1:n.-177_-130del
ENST00000683211.1:c.994_1041del ENSP00000508257.1:p.Val332_Ser347del
ENST00000683250.1:c.404-13468_404-13421del ENSP00000506847.1:n.404-13468_404-13421de...
ENST00000683418.1:n.3341_3388del
ENST00000683678.1:n.994_1041del
ENST00000684153.1:c.649_696del ENSP00000506937.1:p.Val217_Ser232del
ENST00000358487.10:c.994_1041del MANE Select ENSP00000351276.6:p.Val332_Ser347del
ENST00000336553.10:c.727_774del ENSP00000337665.6:p.Val243_Ser258del
ENST00000346997.6:c.994_1041del ENSP00000263451.5:p.Val332_Ser347del
ENST00000351936.10:c.1000_1047del ENSP00000309878.9:p.Val334_Ser349del
ENST00000356226.8:c.649_696del ENSP00000348559.4:p.Val217_Ser232del
ENST00000357555.9:c.727_774del ENSP00000350166.5:p.Val243_Ser258del
ENST00000358487.9:c.994_1041del ENSP00000351276.5:p.Val332_Ser347del
ENST00000360144.7:c.820+1273_820+1320del ENSP00000353262.3:n.820+1273_820+1320del
ENST00000369056.5:c.1087+1273_1087+1320del ENSP00000358052.1:n.1087+1273_1087+1320de...
ENST00000369058.7:c.1087+1273_1087+1320del ENSP00000358054.3:n.1087+1273_1087+1320de...
ENST00000369059.5:c.742+1273_742+1320del ENSP00000358055.1:n.742+1273_742+1320del
ENST00000369060.8:c.939+2570_939+2617del ENSP00000358056.4:n.939+2570_939+2617del
ENST00000369061.8:c.749-2090_749-2043del ENSP00000358057.4:n.749-2090_749-2043del
ENST00000457416.6:c.1087+1273_1087+1320del ENSP00000410294.2:n.1087+1273_1087+1320de...
ENST00000463870.5:n.203_250del
ENST00000478859.5:c.310_357del ENSP00000474011.1:p.Val104_Ser119del
ENST00000490349.5:n.1403_1450del
ENST00000604236.5:c.*41_*88del ENSP00000474109.1:n.*41_*88del
ENST00000613048.4:c.727_774del ENSP00000484154.1:p.Val243_Ser258del
NM_000141.4:c.994_1041del NP_000132.3:p.Val332_Ser347del
NM_001144913.1:c.1087+1273_1087+1320del NP_001138385.1:n.1087+1273_1087+1320del
NM_001144914.1:c.749-2090_749-2043del NP_001138386.1:n.749-2090_749-2043del
NM_001144915.1:c.727_774del NP_001138387.1:p.Val243_Ser258del
NM_001144916.1:c.649_696del NP_001138388.1:p.Val217_Ser232del
NM_001144917.1:c.939+2570_939+2617del NP_001138389.1:n.939+2570_939+2617del
NM_001144918.1:c.649_696del NP_001138390.1:p.Val217_Ser232del
NM_001144919.1:c.820+1273_820+1320del NP_001138391.1:n.820+1273_820+1320del
NM_022970.3:c.1087+1273_1087+1320del NP_075259.4:n.1087+1273_1087+1320del
NM_023029.2:c.727_774del NP_075418.1:p.Val243_Ser258del
NR_073009.1:n.1444_1491del
XM_006717708.2:c.1144+1273_1144+1320del XP_006717771.1:n.1144+1273_1144+1320del
XM_006717709.2:c.1051_1098del XP_006717772.1:p.Val351_Ser366del
XM_006717710.2:c.1144+1273_1144+1320del XP_006717773.1:n.1144+1273_1144+1320del
XM_006717711.2:c.877+1273_877+1320del XP_006717774.1:n.877+1273_877+1320del
XM_006717712.2:c.799+1273_799+1320del XP_006717775.1:n.799+1273_799+1320del
XM_006717713.2:c.1051_1098del XP_006717776.1:p.Val351_Ser366del
XM_011539510.1:c.310_357del XP_011537812.1:p.Val104_Ser119del
NM_001320654.1:c.310_357del NP_001307583.1:p.Val104_Ser119del
NM_001320658.1:c.994_1041del NP_001307587.1:p.Val332_Ser347del
XM_006717708.3:c.1144+1273_1144+1320del XP_006717771.1:n.1144+1273_1144+1320del
XM_006717710.4:c.1144+1273_1144+1320del XP_006717773.1:n.1144+1273_1144+1320del
XM_017015920.2:c.1144+1273_1144+1320del XP_016871409.1:n.1144+1273_1144+1320del
XM_017015921.2:c.1051_1098del XP_016871410.1:p.Val351_Ser366del
XM_017015924.2:c.706_753del XP_016871413.1:p.Val236_Ser251del
XM_017015925.2:c.706_753del XP_016871414.1:p.Val236_Ser251del
XM_024447887.1:c.784_831del XP_024303655.1:p.Val262_Ser277del
XM_024447888.1:c.877+1273_877+1320del XP_024303656.1:n.877+1273_877+1320del
XM_024447889.1:c.784_831del XP_024303657.1:p.Val262_Ser277del
XM_024447890.1:c.877+1273_877+1320del XP_024303658.1:n.877+1273_877+1320del
XM_024447891.1:c.799+1273_799+1320del XP_024303659.1:n.799+1273_799+1320del
XM_024447892.1:c.-177_-130del XP_024303660.1:n.-177_-130del
NM_000141.5:c.994_1041del MANE Select NP_000132.3:p.Val332_Ser347del
NM_001144917.2:c.939+2570_939+2617del NP_001138389.1:n.939+2570_939+2617del
NM_001144918.2:c.649_696del NP_001138390.1:p.Val217_Ser232del
NM_001144919.2:c.820+1273_820+1320del NP_001138391.1:n.820+1273_820+1320del
NM_001320658.2:c.994_1041del NP_001307587.1:p.Val332_Ser347del
NR_073009.2:n.1430_1477del
NM_001144915.2:c.727_774del NP_001138387.1:p.Val243_Ser258del
NM_001144916.2:c.649_696del NP_001138388.1:p.Val217_Ser232del
NM_001320654.2:c.310_357del NP_001307583.1:p.Val104_Ser119del