Canonical Allele Identifier: CA378358498
Community Standard Title: NM_000141.5(FGFR2):c.2428C>G (p.Pro810Ala)
Gene: FGFR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121479895G>C , CM000672.2:g.121479895G>C GRCh38
NC_000010.10:g.123239409G>C , CM000672.1:g.123239409G>C GRCh37
NC_000010.9:g.123229399G>C NCBI36
NG_012449.1:g.123564C>G
NG_012449.2:g.123564C>G

Transcript Alleles

HGVS Amino-acid Change
NM_000141.5:c.2428C>G MANE Select NP_000132.3:p.Pro810Ala
ENST00000358487.10:c.2428C>G MANE Select ENSP00000351276.6:p.Pro810Ala
ENST00000457416.7:c.2431C>G MANE Plus Clinical ENSP00000410294.2:p.Pro811Ala
NM_000141.4:c.2428C>G NP_000132.3:p.Pro810Ala
NM_001144914.1:c.2092C>G NP_001138386.1:p.Pro698Ala
NM_001144915.1:c.2035-225C>G NP_001138387.1:n.2035-225C>G
NM_001144915.2:c.2035-225C>G NP_001138387.1:n.2035-225C>G
NM_001144916.1:c.2083C>G NP_001138388.1:p.Pro695Ala
NM_001144916.2:c.2083C>G NP_001138388.1:p.Pro695Ala
NM_001144917.1:c.2080C>G NP_001138389.1:p.Pro694Ala
NM_001144917.2:c.2080C>G NP_001138389.1:p.Pro694Ala
NM_001144918.1:c.2077C>G NP_001138390.1:p.Pro693Ala
NM_001144918.2:c.2077C>G NP_001138390.1:p.Pro693Ala
NM_001320654.1:c.1744C>G NP_001307583.1:p.Pro582Ala
NM_001320654.2:c.1744C>G NP_001307583.1:p.Pro582Ala
NM_001320658.1:c.2422C>G NP_001307587.1:p.Pro808Ala
NM_001320658.2:c.2422C>G NP_001307587.1:p.Pro808Ala
NM_022970.3:c.2431C>G NP_075259.4:p.Pro811Ala
NM_023029.2:c.2161C>G NP_075418.1:p.Pro721Ala
NR_073009.1:n.2878C>G
NR_073009.2:n.2864C>G
ENST00000346997.6:c.2422C>G ENSP00000263451.5:p.Pro808Ala
ENST00000351936.10:c.2428C>G ENSP00000309878.9:p.Pro810Ala
ENST00000351936.11:c.2422C>G ENSP00000309878.10:p.Pro808Ala
ENST00000356226.8:c.2077C>G ENSP00000348559.4:p.Pro693Ala
ENST00000357555.9:c.2035-225C>G ENSP00000350166.5:n.2035-225C>G
ENST00000358487.9:c.2428C>G ENSP00000351276.5:p.Pro810Ala
ENST00000369059.5:c.2086C>G ENSP00000358055.1:p.Pro696Ala
ENST00000369060.8:c.2080C>G ENSP00000358056.4:p.Pro694Ala
ENST00000369061.8:c.2092C>G ENSP00000358057.4:p.Pro698Ala
ENST00000429361.5:c.1098C>G ENSP00000404219.1:p.Phe366Leu
ENST00000457416.6:c.2431C>G ENSP00000410294.2:p.Pro811Ala
ENST00000467584.1:n.387C>G
ENST00000478859.5:c.1744C>G ENSP00000474011.1:p.Pro582Ala
ENST00000604236.5:c.*1475C>G ENSP00000474109.1:n.*1475C>G
ENST00000613048.4:c.2161C>G ENSP00000484154.1:p.Pro721Ala
ENST00000638709.1:c.415C>G
ENST00000638709.2:c.1252C>G ENSP00000491912.2:p.Pro418Ala
ENST00000682296.1:n.1770C>G
ENST00000682550.1:c.2077C>G ENSP00000507633.1:p.Pro693Ala
ENST00000682772.1:c.1252C>G ENSP00000506848.1:p.Pro418Ala
ENST00000682904.1:n.1248C>G
ENST00000683029.1:n.2431C>G
ENST00000683211.1:c.2422C>G ENSP00000508257.1:p.Pro808Ala
ENST00000683250.1:c.*2721C>G ENSP00000506847.1:n.*2721C>G
ENST00000683418.1:n.4769C>G
ENST00000684153.1:c.*156C>G ENSP00000506937.1:n.*156C>G
ENST00000684516.1:n.3441C>G
XM_006717708.2:c.2482C>G XP_006717771.1:p.Pro828Ala
XM_006717708.3:c.2482C>G XP_006717771.1:p.Pro828Ala
XM_006717709.2:c.2479C>G XP_006717772.1:p.Pro827Ala
XM_006717710.2:c.*156C>G XP_006717773.1:n.*156C>G
XM_006717710.4:c.*156C>G XP_006717773.1:n.*156C>G
XM_006717711.2:c.2221C>G XP_006717774.1:p.Pro741Ala
XM_006717712.2:c.2143C>G XP_006717775.1:p.Pro715Ala
XM_006717713.2:c.*156C>G XP_006717776.1:n.*156C>G
XM_011539510.1:c.1744C>G XP_011537812.1:p.Pro582Ala
XM_017015920.2:c.*156C>G XP_016871409.1:n.*156C>G
XM_017015921.2:c.*156C>G XP_016871410.1:n.*156C>G
XM_017015924.2:c.2140C>G XP_016871413.1:p.Pro714Ala
XM_017015925.2:c.*156C>G XP_016871414.1:n.*156C>G
XM_024447887.1:c.2218C>G XP_024303655.1:p.Pro740Ala
XM_024447888.1:c.2215C>G XP_024303656.1:p.Pro739Ala
XM_024447889.1:c.2212C>G XP_024303657.1:p.Pro738Ala
XM_024447890.1:c.2221C>G XP_024303658.1:p.Pro741Ala
XM_024447891.1:c.2143C>G XP_024303659.1:p.Pro715Ala
XM_024447892.1:c.1258C>G XP_024303660.1:p.Pro420Ala