Canonical Allele Identifier: CA1941017714
Gene: FGFR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121498556C= , CM000672.2:g.121498556C= GRCh38
NC_000010.10:g.123258070C= , CM000672.1:g.123258070C= GRCh37
NC_000010.9:g.123248060C= NCBI36
NG_012449.1:g.104903G=
NG_012449.2:g.104903G=

Transcript Alleles

HGVS Amino-acid Change
NM_000141.5:c.1611G= MANE Select NP_000132.3:p.Met537=
ENST00000358487.10:c.1611G= MANE Select ENSP00000351276.6:p.Met537=
ENST00000457416.7:c.1614G= MANE Plus Clinical ENSP00000410294.2:p.Met538=
NM_000141.4:c.1611G= NP_000132.3:p.Met537=
NM_001144913.1:c.1614G= NP_001138385.1:p.Met538=
NM_001144914.1:c.1275G= NP_001138386.1:p.Met425=
NM_001144915.1:c.1344G= NP_001138387.1:p.Met448=
NM_001144915.2:c.1344G= NP_001138387.1:p.Met448=
NM_001144916.1:c.1266G= NP_001138388.1:p.Met422=
NM_001144916.2:c.1266G= NP_001138388.1:p.Met422=
NM_001144917.1:c.1263G= NP_001138389.1:p.Met421=
NM_001144917.2:c.1263G= NP_001138389.1:p.Met421=
NM_001144918.1:c.1260G= NP_001138390.1:p.Met420=
NM_001144918.2:c.1260G= NP_001138390.1:p.Met420=
NM_001144919.1:c.1347G= NP_001138391.1:p.Met449=
NM_001144919.2:c.1347G= NP_001138391.1:p.Met449=
NM_001320654.1:c.927G= NP_001307583.1:p.Met309=
NM_001320654.2:c.927G= NP_001307583.1:p.Met309=
NM_001320658.1:c.1605G= NP_001307587.1:p.Met535=
NM_001320658.2:c.1605G= NP_001307587.1:p.Met535=
NM_022970.3:c.1614G= NP_075259.4:p.Met538=
NM_023029.2:c.1344G= NP_075418.1:p.Met448=
NR_073009.1:n.2061G=
NR_073009.2:n.2047G=
ENST00000336553.10:c.1338G= ENSP00000337665.6:p.Met446=
ENST00000346997.6:c.1605G= ENSP00000263451.5:p.Met535=
ENST00000351936.10:c.1611G= ENSP00000309878.9:p.Met537=
ENST00000351936.11:c.1605G= ENSP00000309878.10:p.Met535=
ENST00000356226.8:c.1260G= ENSP00000348559.4:p.Met420=
ENST00000357555.9:c.1344G= ENSP00000350166.5:p.Met448=
ENST00000358487.9:c.1611G= ENSP00000351276.5:p.Met537=
ENST00000360144.7:c.1347G= ENSP00000353262.3:p.Met449=
ENST00000369056.5:c.1614G= ENSP00000358052.1:p.Met538=
ENST00000369058.7:c.1614G= ENSP00000358054.3:p.Met538=
ENST00000369059.5:c.1269G= ENSP00000358055.1:p.Met423=
ENST00000369060.8:c.1263G= ENSP00000358056.4:p.Met421=
ENST00000369061.8:c.1275G= ENSP00000358057.4:p.Met425=
ENST00000429361.5:c.387G= ENSP00000404219.1:p.Met129=
ENST00000457416.6:c.1614G= ENSP00000410294.2:p.Met538=
ENST00000478859.5:c.927G= ENSP00000474011.1:p.Met309=
ENST00000604236.5:c.*658G= ENSP00000474109.1:n.*658G=
ENST00000613048.4:c.1344G= ENSP00000484154.1:p.Met448=
ENST00000638709.2:c.435G= ENSP00000491912.2:p.Met145=
ENST00000682296.1:n.953G=
ENST00000682550.1:c.1260G= ENSP00000507633.1:p.Met420=
ENST00000682772.1:c.435G= ENSP00000506848.1:p.Met145=
ENST00000682904.1:n.431G=
ENST00000683211.1:c.1605G= ENSP00000508257.1:p.Met535=
ENST00000683250.1:c.*313G= ENSP00000506847.1:n.*313G=
ENST00000683418.1:n.3952G=
ENST00000684153.1:c.1260G= ENSP00000506937.1:p.Met420=
ENST00000684516.1:n.2624G=
XM_006717708.2:c.1665G= XP_006717771.1:p.Met555=
XM_006717708.3:c.1665G= XP_006717771.1:p.Met555=
XM_006717709.2:c.1662G= XP_006717772.1:p.Met554=
XM_006717710.2:c.1671G= XP_006717773.1:p.Met557=
XM_006717710.4:c.1671G= XP_006717773.1:p.Met557=
XM_006717711.2:c.1404G= XP_006717774.1:p.Met468=
XM_006717712.2:c.1326G= XP_006717775.1:p.Met442=
XM_006717713.2:c.1668G= XP_006717776.1:p.Met556=
XM_011539510.1:c.927G= XP_011537812.1:p.Met309=
XM_017015920.2:c.1665G= XP_016871409.1:p.Met555=
XM_017015921.2:c.1662G= XP_016871410.1:p.Met554=
XM_017015924.2:c.1323G= XP_016871413.1:p.Met441=
XM_017015925.2:c.1317G= XP_016871414.1:p.Met439=
XM_024447887.1:c.1401G= XP_024303655.1:p.Met467=
XM_024447888.1:c.1398G= XP_024303656.1:p.Met466=
XM_024447889.1:c.1395G= XP_024303657.1:p.Met465=
XM_024447890.1:c.1404G= XP_024303658.1:p.Met468=
XM_024447891.1:c.1326G= XP_024303659.1:p.Met442=
XM_024447892.1:c.441G= XP_024303660.1:p.Met147=