Canonical Allele Identifier: CA1941016790
Community Standard Title: NM_000141.5(FGFR2):c.1694A= (p.Glu565=)
Gene: FGFR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121496701T= , CM000672.2:g.121496701T= GRCh38
NC_000010.10:g.123256215T= , CM000672.1:g.123256215T= GRCh37
NC_000010.9:g.123246205T= NCBI36
NG_012449.1:g.106758A=
NG_012449.2:g.106758A=

Transcript Alleles

HGVS Amino-acid Change
NM_000141.5:c.1694A= MANE Select NP_000132.3:p.Glu565=
ENST00000358487.10:c.1694A= MANE Select ENSP00000351276.6:p.Glu565=
ENST00000457416.7:c.1697A= MANE Plus Clinical ENSP00000410294.2:p.Glu566=
NM_000141.4:c.1694A= NP_000132.3:p.Glu565=
NM_001144913.1:c.1697A= NP_001138385.1:p.Glu566=
NM_001144914.1:c.1358A= NP_001138386.1:p.Glu453=
NM_001144915.1:c.1427A= NP_001138387.1:p.Glu476=
NM_001144915.2:c.1427A= NP_001138387.1:p.Glu476=
NM_001144916.1:c.1349A= NP_001138388.1:p.Glu450=
NM_001144916.2:c.1349A= NP_001138388.1:p.Glu450=
NM_001144917.1:c.1346A= NP_001138389.1:p.Glu449=
NM_001144917.2:c.1346A= NP_001138389.1:p.Glu449=
NM_001144918.1:c.1343A= NP_001138390.1:p.Glu448=
NM_001144918.2:c.1343A= NP_001138390.1:p.Glu448=
NM_001144919.1:c.1430A= NP_001138391.1:p.Glu477=
NM_001144919.2:c.1430A= NP_001138391.1:p.Glu477=
NM_001320654.1:c.1010A= NP_001307583.1:p.Glu337=
NM_001320654.2:c.1010A= NP_001307583.1:p.Glu337=
NM_001320658.1:c.1688A= NP_001307587.1:p.Glu563=
NM_001320658.2:c.1688A= NP_001307587.1:p.Glu563=
NM_022970.3:c.1697A= NP_075259.4:p.Glu566=
NM_023029.2:c.1427A= NP_075418.1:p.Glu476=
NR_073009.1:n.2144A=
NR_073009.2:n.2130A=
ENST00000336553.10:c.1421A= ENSP00000337665.6:p.Glu474=
ENST00000346997.6:c.1688A= ENSP00000263451.5:p.Glu563=
ENST00000351936.10:c.1694A= ENSP00000309878.9:p.Glu565=
ENST00000351936.11:c.1688A= ENSP00000309878.10:p.Glu563=
ENST00000356226.8:c.1343A= ENSP00000348559.4:p.Glu448=
ENST00000357555.9:c.1427A= ENSP00000350166.5:p.Glu476=
ENST00000358487.9:c.1694A= ENSP00000351276.5:p.Glu565=
ENST00000360144.7:c.1430A= ENSP00000353262.3:p.Glu477=
ENST00000369056.5:c.1697A= ENSP00000358052.1:p.Glu566=
ENST00000369058.7:c.1697A= ENSP00000358054.3:p.Glu566=
ENST00000369059.5:c.1352A= ENSP00000358055.1:p.Glu451=
ENST00000369060.8:c.1346A= ENSP00000358056.4:p.Glu449=
ENST00000369061.8:c.1358A= ENSP00000358057.4:p.Glu453=
ENST00000429361.5:c.470A= ENSP00000404219.1:p.Glu157=
ENST00000457416.6:c.1697A= ENSP00000410294.2:p.Glu566=
ENST00000478859.5:c.1010A= ENSP00000474011.1:p.Glu337=
ENST00000604236.5:c.*741A= ENSP00000474109.1:n.*741A=
ENST00000613048.4:c.1427A= ENSP00000484154.1:p.Glu476=
ENST00000638709.2:c.518A= ENSP00000491912.2:p.Glu173=
ENST00000682296.1:n.1036A=
ENST00000682550.1:c.1343A= ENSP00000507633.1:p.Glu448=
ENST00000682772.1:c.518A= ENSP00000506848.1:p.Glu173=
ENST00000682904.1:n.514A=
ENST00000683029.1:n.106A=
ENST00000683211.1:c.1688A= ENSP00000508257.1:p.Glu563=
ENST00000683250.1:c.*396A= ENSP00000506847.1:n.*396A=
ENST00000683418.1:n.4035A=
ENST00000684153.1:c.1343A= ENSP00000506937.1:p.Glu448=
ENST00000684516.1:n.2707A=
XM_006717708.2:c.1748A= XP_006717771.1:p.Glu583=
XM_006717708.3:c.1748A= XP_006717771.1:p.Glu583=
XM_006717709.2:c.1745A= XP_006717772.1:p.Glu582=
XM_006717710.2:c.1754A= XP_006717773.1:p.Glu585=
XM_006717710.4:c.1754A= XP_006717773.1:p.Glu585=
XM_006717711.2:c.1487A= XP_006717774.1:p.Glu496=
XM_006717712.2:c.1409A= XP_006717775.1:p.Glu470=
XM_006717713.2:c.1751A= XP_006717776.1:p.Glu584=
XM_011539510.1:c.1010A= XP_011537812.1:p.Glu337=
XM_017015920.2:c.1748A= XP_016871409.1:p.Glu583=
XM_017015921.2:c.1745A= XP_016871410.1:p.Glu582=
XM_017015924.2:c.1406A= XP_016871413.1:p.Glu469=
XM_017015925.2:c.1400A= XP_016871414.1:p.Glu467=
XM_024447887.1:c.1484A= XP_024303655.1:p.Glu495=
XM_024447888.1:c.1481A= XP_024303656.1:p.Glu494=
XM_024447889.1:c.1478A= XP_024303657.1:p.Glu493=
XM_024447890.1:c.1487A= XP_024303658.1:p.Glu496=
XM_024447891.1:c.1409A= XP_024303659.1:p.Glu470=
XM_024447892.1:c.524A= XP_024303660.1:p.Glu175=