Canonical Allele Identifier: CA378358663
Gene: FGFR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121479955A>G , CM000672.2:g.121479955A>G GRCh38
NC_000010.10:g.123239469A>G , CM000672.1:g.123239469A>G GRCh37
NC_000010.9:g.123229459A>G NCBI36
NG_012449.1:g.123504T>C
NG_012449.2:g.123504T>C

Transcript Alleles

HGVS Amino-acid Change
NM_000141.5:c.2368T>C MANE Select NP_000132.3:p.Cys790Arg
ENST00000358487.10:c.2368T>C MANE Select ENSP00000351276.6:p.Cys790Arg
ENST00000457416.7:c.2371T>C MANE Plus Clinical ENSP00000410294.2:p.Cys791Arg
NM_000141.4:c.2368T>C NP_000132.3:p.Cys790Arg
NM_001144914.1:c.2032T>C NP_001138386.1:p.Cys678Arg
NM_001144915.1:c.2035-285T>C NP_001138387.1:n.2035-285T>C
NM_001144915.2:c.2035-285T>C NP_001138387.1:n.2035-285T>C
NM_001144916.1:c.2023T>C NP_001138388.1:p.Cys675Arg
NM_001144916.2:c.2023T>C NP_001138388.1:p.Cys675Arg
NM_001144917.1:c.2020T>C NP_001138389.1:p.Cys674Arg
NM_001144917.2:c.2020T>C NP_001138389.1:p.Cys674Arg
NM_001144918.1:c.2017T>C NP_001138390.1:p.Cys673Arg
NM_001144918.2:c.2017T>C NP_001138390.1:p.Cys673Arg
NM_001320654.1:c.1684T>C NP_001307583.1:p.Cys562Arg
NM_001320654.2:c.1684T>C NP_001307583.1:p.Cys562Arg
NM_001320658.1:c.2362T>C NP_001307587.1:p.Cys788Arg
NM_001320658.2:c.2362T>C NP_001307587.1:p.Cys788Arg
NM_022970.3:c.2371T>C NP_075259.4:p.Cys791Arg
NM_023029.2:c.2101T>C NP_075418.1:p.Cys701Arg
NR_073009.1:n.2818T>C
NR_073009.2:n.2804T>C
ENST00000346997.6:c.2362T>C ENSP00000263451.5:p.Cys788Arg
ENST00000351936.10:c.2368T>C ENSP00000309878.9:p.Cys790Arg
ENST00000351936.11:c.2362T>C ENSP00000309878.10:p.Cys788Arg
ENST00000356226.8:c.2017T>C ENSP00000348559.4:p.Cys673Arg
ENST00000357555.9:c.2035-285T>C ENSP00000350166.5:n.2035-285T>C
ENST00000358487.9:c.2368T>C ENSP00000351276.5:p.Cys790Arg
ENST00000369059.5:c.2026T>C ENSP00000358055.1:p.Cys676Arg
ENST00000369060.8:c.2020T>C ENSP00000358056.4:p.Cys674Arg
ENST00000369061.8:c.2032T>C ENSP00000358057.4:p.Cys678Arg
ENST00000429361.5:c.1038T>C ENSP00000404219.1:p.Leu346=
ENST00000457416.6:c.2371T>C ENSP00000410294.2:p.Cys791Arg
ENST00000467584.1:n.327T>C
ENST00000478859.5:c.1684T>C ENSP00000474011.1:p.Cys562Arg
ENST00000604236.5:c.*1415T>C ENSP00000474109.1:n.*1415T>C
ENST00000613048.4:c.2101T>C ENSP00000484154.1:p.Cys701Arg
ENST00000638709.1:c.355T>C
ENST00000638709.2:c.1192T>C ENSP00000491912.2:p.Cys398Arg
ENST00000682296.1:n.1710T>C
ENST00000682550.1:c.2017T>C ENSP00000507633.1:p.Cys673Arg
ENST00000682772.1:c.1192T>C ENSP00000506848.1:p.Cys398Arg
ENST00000682904.1:n.1188T>C
ENST00000683029.1:n.2371T>C
ENST00000683211.1:c.2362T>C ENSP00000508257.1:p.Cys788Arg
ENST00000683250.1:c.*2661T>C ENSP00000506847.1:n.*2661T>C
ENST00000683418.1:n.4709T>C
ENST00000684153.1:c.*96T>C ENSP00000506937.1:n.*96T>C
ENST00000684516.1:n.3381T>C
XM_006717708.2:c.2422T>C XP_006717771.1:p.Cys808Arg
XM_006717708.3:c.2422T>C XP_006717771.1:p.Cys808Arg
XM_006717709.2:c.2419T>C XP_006717772.1:p.Cys807Arg
XM_006717710.2:c.*96T>C XP_006717773.1:n.*96T>C
XM_006717710.4:c.*96T>C XP_006717773.1:n.*96T>C
XM_006717711.2:c.2161T>C XP_006717774.1:p.Cys721Arg
XM_006717712.2:c.2083T>C XP_006717775.1:p.Cys695Arg
XM_006717713.2:c.*96T>C XP_006717776.1:n.*96T>C
XM_011539510.1:c.1684T>C XP_011537812.1:p.Cys562Arg
XM_017015920.2:c.*96T>C XP_016871409.1:n.*96T>C
XM_017015921.2:c.*96T>C XP_016871410.1:n.*96T>C
XM_017015924.2:c.2080T>C XP_016871413.1:p.Cys694Arg
XM_017015925.2:c.*96T>C XP_016871414.1:n.*96T>C
XM_024447887.1:c.2158T>C XP_024303655.1:p.Cys720Arg
XM_024447888.1:c.2155T>C XP_024303656.1:p.Cys719Arg
XM_024447889.1:c.2152T>C XP_024303657.1:p.Cys718Arg
XM_024447890.1:c.2161T>C XP_024303658.1:p.Cys721Arg
XM_024447891.1:c.2083T>C XP_024303659.1:p.Cys695Arg
XM_024447892.1:c.1198T>C XP_024303660.1:p.Cys400Arg