Canonical Allele Identifier: CA1941023739
Gene: FGFR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121515289G= , CM000672.2:g.121515289G= GRCh38
NC_000010.10:g.123274803G= , CM000672.1:g.123274803G= GRCh37
NC_000010.9:g.123264793G= NCBI36
NG_012449.1:g.88170C=
NG_012449.2:g.88170C=

Transcript Alleles

HGVS Amino-acid Change
NM_000141.5:c.1115C= MANE Select NP_000132.3:p.Ser372=
ENST00000358487.10:c.1115C= MANE Select ENSP00000351276.6:p.Ser372=
ENST00000457416.7:c.1118C= MANE Plus Clinical ENSP00000410294.2:p.Ser373=
NM_000141.4:c.1115C= NP_000132.3:p.Ser372=
NM_001144913.1:c.1118C= NP_001138385.1:p.Ser373=
NM_001144914.1:c.779C= NP_001138386.1:p.Ser260=
NM_001144915.1:c.848C= NP_001138387.1:p.Ser283=
NM_001144915.2:c.848C= NP_001138387.1:p.Ser283=
NM_001144916.1:c.770C= NP_001138388.1:p.Ser257=
NM_001144916.2:c.770C= NP_001138388.1:p.Ser257=
NM_001144917.1:c.939+4690C= NP_001138389.1:n.939+4690C=
NM_001144917.2:c.939+4690C= NP_001138389.1:n.939+4690C=
NM_001144918.1:c.770C= NP_001138390.1:p.Ser257=
NM_001144918.2:c.770C= NP_001138390.1:p.Ser257=
NM_001144919.1:c.851C= NP_001138391.1:p.Ser284=
NM_001144919.2:c.851C= NP_001138391.1:p.Ser284=
NM_001320654.1:c.431C= NP_001307583.1:p.Ser144=
NM_001320654.2:c.431C= NP_001307583.1:p.Ser144=
NM_001320658.1:c.1115C= NP_001307587.1:p.Ser372=
NM_001320658.2:c.1115C= NP_001307587.1:p.Ser372=
NM_022970.3:c.1118C= NP_075259.4:p.Ser373=
NM_023029.2:c.848C= NP_075418.1:p.Ser283=
NR_073009.1:n.1565C=
NR_073009.2:n.1551C=
ENST00000336553.10:c.848C= ENSP00000337665.6:p.Ser283=
ENST00000346997.6:c.1115C= ENSP00000263451.5:p.Ser372=
ENST00000351936.10:c.1121C= ENSP00000309878.9:p.Ser374=
ENST00000351936.11:c.1115C= ENSP00000309878.10:p.Ser372=
ENST00000356226.8:c.770C= ENSP00000348559.4:p.Ser257=
ENST00000357555.9:c.848C= ENSP00000350166.5:p.Ser283=
ENST00000358487.9:c.1115C= ENSP00000351276.5:p.Ser372=
ENST00000360144.7:c.851C= ENSP00000353262.3:p.Ser284=
ENST00000369056.5:c.1118C= ENSP00000358052.1:p.Ser373=
ENST00000369058.7:c.1118C= ENSP00000358054.3:p.Ser373=
ENST00000369059.5:c.773C= ENSP00000358055.1:p.Ser258=
ENST00000369060.8:c.939+4690C= ENSP00000358056.4:n.939+4690C=
ENST00000369061.8:c.779C= ENSP00000358057.4:p.Ser260=
ENST00000457416.6:c.1118C= ENSP00000410294.2:p.Ser373=
ENST00000463870.5:n.324C=
ENST00000478859.5:c.431C= ENSP00000474011.1:p.Ser144=
ENST00000604236.5:c.*162C= ENSP00000474109.1:n.*162C=
ENST00000613048.4:c.848C= ENSP00000484154.1:p.Ser283=
ENST00000638709.2:c.-56C= ENSP00000491912.2:n.-56C=
ENST00000682296.1:n.463C=
ENST00000682550.1:c.770C= ENSP00000507633.1:p.Ser257=
ENST00000682772.1:c.-56C= ENSP00000506848.1:n.-56C=
ENST00000683211.1:c.1115C= ENSP00000508257.1:p.Ser372=
ENST00000683250.1:c.404-11348C= ENSP00000506847.1:n.404-11348C=
ENST00000683418.1:n.3462C=
ENST00000684153.1:c.770C= ENSP00000506937.1:p.Ser257=
XM_006717708.2:c.1175C= XP_006717771.1:p.Ser392=
XM_006717708.3:c.1175C= XP_006717771.1:p.Ser392=
XM_006717709.2:c.1172C= XP_006717772.1:p.Ser391=
XM_006717710.2:c.1175C= XP_006717773.1:p.Ser392=
XM_006717710.4:c.1175C= XP_006717773.1:p.Ser392=
XM_006717711.2:c.908C= XP_006717774.1:p.Ser303=
XM_006717712.2:c.830C= XP_006717775.1:p.Ser277=
XM_006717713.2:c.1172C= XP_006717776.1:p.Ser391=
XM_011539510.1:c.431C= XP_011537812.1:p.Ser144=
XM_017015920.2:c.1175C= XP_016871409.1:p.Ser392=
XM_017015921.2:c.1172C= XP_016871410.1:p.Ser391=
XM_017015924.2:c.827C= XP_016871413.1:p.Ser276=
XM_017015925.2:c.827C= XP_016871414.1:p.Ser276=
XM_024447887.1:c.905C= XP_024303655.1:p.Ser302=
XM_024447888.1:c.908C= XP_024303656.1:p.Ser303=
XM_024447889.1:c.905C= XP_024303657.1:p.Ser302=
XM_024447890.1:c.908C= XP_024303658.1:p.Ser303=
XM_024447891.1:c.830C= XP_024303659.1:p.Ser277=
XM_024447892.1:c.-56C= XP_024303660.1:n.-56C=