Canonical Allele Identifier: CA128693

Gene: FGFR2

Linked Data

• ClinVar Variation Id: 29855
• ClinVar RCV Id: RCV000022734 ; RCV000493423
• dbSNP Id: rs387906677
• COSMIC: COSM36907
• MyVariant Identifiers: chr10:g.123274746A>C (hg19) ; chr10:g.121515232A>C (hg38)
• PubMed: PMID:22387015

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121515232A>C , CM000672.2:g.121515232A>C	GRCh38
NC_000010.10:g.123274746A>C , CM000672.1:g.123274746A>C	GRCh37
NC_000010.9:g.123264736A>C	NCBI36
NG_012449.1:g.88227T>G
NG_012449.2:g.88227T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000457416.7:c.1175T>G MANE Plus Clinical	ENSP00000410294.2:p.Met392Arg
ENST00000351936.11:c.1172T>G	ENSP00000309878.10:p.Met391Arg
ENST00000638709.2:c.2T>G	ENSP00000491912.2:p.Met1Arg
ENST00000682296.1:n.520T>G
ENST00000682550.1:c.827T>G	ENSP00000507633.1:p.Met276Arg
ENST00000682772.1:c.2T>G	ENSP00000506848.1:p.Met1Arg
ENST00000683211.1:c.1172T>G	ENSP00000508257.1:p.Met391Arg
ENST00000683250.1:c.404-11291T>G	ENSP00000506847.1:n.404-11291T>G
ENST00000683418.1:n.3519T>G
ENST00000684153.1:c.827T>G	ENSP00000506937.1:p.Met276Arg
ENST00000358487.10:c.1172T>G MANE Select	ENSP00000351276.6:p.Met391Arg
ENST00000336553.10:c.905T>G	ENSP00000337665.6:p.Met302Arg
ENST00000346997.6:c.1172T>G	ENSP00000263451.5:p.Met391Arg
ENST00000351936.10:c.1178T>G	ENSP00000309878.9:p.Met393Arg
ENST00000356226.8:c.827T>G	ENSP00000348559.4:p.Met276Arg
ENST00000357555.9:c.905T>G	ENSP00000350166.5:p.Met302Arg
ENST00000358487.9:c.1172T>G	ENSP00000351276.5:p.Met391Arg
ENST00000360144.7:c.908T>G	ENSP00000353262.3:p.Met303Arg
ENST00000369056.5:c.1175T>G	ENSP00000358052.1:p.Met392Arg
ENST00000369058.7:c.1175T>G	ENSP00000358054.3:p.Met392Arg
ENST00000369059.5:c.830T>G	ENSP00000358055.1:p.Met277Arg
ENST00000369060.8:c.939+4747T>G	ENSP00000358056.4:n.939+4747T>G
ENST00000369061.8:c.836T>G	ENSP00000358057.4:p.Met279Arg
ENST00000457416.6:c.1175T>G	ENSP00000410294.2:p.Met392Arg
ENST00000463870.5:n.381T>G
ENST00000478859.5:c.488T>G	ENSP00000474011.1:p.Met163Arg
ENST00000604236.5:c.*219T>G	ENSP00000474109.1:n.*219T>G
ENST00000613048.4:c.905T>G	ENSP00000484154.1:p.Met302Arg
NM_000141.4:c.1172T>G	NP_000132.3:p.Met391Arg
NM_001144913.1:c.1175T>G	NP_001138385.1:p.Met392Arg
NM_001144914.1:c.836T>G	NP_001138386.1:p.Met279Arg
NM_001144915.1:c.905T>G	NP_001138387.1:p.Met302Arg
NM_001144916.1:c.827T>G	NP_001138388.1:p.Met276Arg
NM_001144917.1:c.939+4747T>G	NP_001138389.1:n.939+4747T>G
NM_001144918.1:c.827T>G	NP_001138390.1:p.Met276Arg
NM_001144919.1:c.908T>G	NP_001138391.1:p.Met303Arg
NM_022970.3:c.1175T>G	NP_075259.4:p.Met392Arg
NM_023029.2:c.905T>G	NP_075418.1:p.Met302Arg
NR_073009.1:n.1622T>G
XM_006717708.2:c.1232T>G	XP_006717771.1:p.Met411Arg
XM_006717709.2:c.1229T>G	XP_006717772.1:p.Met410Arg
XM_006717710.2:c.1232T>G	XP_006717773.1:p.Met411Arg
XM_006717711.2:c.965T>G	XP_006717774.1:p.Met322Arg
XM_006717712.2:c.887T>G	XP_006717775.1:p.Met296Arg
XM_006717713.2:c.1229T>G	XP_006717776.1:p.Met410Arg
XM_011539510.1:c.488T>G	XP_011537812.1:p.Met163Arg
NM_001320654.1:c.488T>G	NP_001307583.1:p.Met163Arg
NM_001320658.1:c.1172T>G	NP_001307587.1:p.Met391Arg
XM_006717708.3:c.1232T>G	XP_006717771.1:p.Met411Arg
XM_006717710.4:c.1232T>G	XP_006717773.1:p.Met411Arg
XM_017015920.2:c.1232T>G	XP_016871409.1:p.Met411Arg
XM_017015921.2:c.1229T>G	XP_016871410.1:p.Met410Arg
XM_017015924.2:c.884T>G	XP_016871413.1:p.Met295Arg
XM_017015925.2:c.884T>G	XP_016871414.1:p.Met295Arg
XM_024447887.1:c.962T>G	XP_024303655.1:p.Met321Arg
XM_024447888.1:c.965T>G	XP_024303656.1:p.Met322Arg
XM_024447889.1:c.962T>G	XP_024303657.1:p.Met321Arg
XM_024447890.1:c.965T>G	XP_024303658.1:p.Met322Arg
XM_024447891.1:c.887T>G	XP_024303659.1:p.Met296Arg
XM_024447892.1:c.2T>G	XP_024303660.1:p.Met1Arg
NM_000141.5:c.1172T>G MANE Select	NP_000132.3:p.Met391Arg
NM_001144917.2:c.939+4747T>G	NP_001138389.1:n.939+4747T>G
NM_001144918.2:c.827T>G	NP_001138390.1:p.Met276Arg
NM_001144919.2:c.908T>G	NP_001138391.1:p.Met303Arg
NM_001320658.2:c.1172T>G	NP_001307587.1:p.Met391Arg
NR_073009.2:n.1608T>G
NM_001144915.2:c.905T>G	NP_001138387.1:p.Met302Arg
NM_001144916.2:c.827T>G	NP_001138388.1:p.Met276Arg
NM_001320654.2:c.488T>G	NP_001307583.1:p.Met163Arg