Canonical Allele Identifier: CA471647435

Gene: FGFR2

Linked Data

• dbSNP Id: rs2133839671
• MyVariant Identifiers: chr10:g.123247622A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121488108A>T , CM000672.2:g.121488108A>T	GRCh38
NC_000010.10:g.123247622A>T , CM000672.1:g.123247622A>T	GRCh37
NC_000010.9:g.123237612A>T	NCBI36
NG_012449.1:g.115351T>A
NG_012449.2:g.115351T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000457416.7:c.1872T>A MANE Plus Clinical	ENSP00000410294.2:p.Ile624=
ENST00000351936.11:c.1863T>A	ENSP00000309878.10:p.Ile621=
ENST00000638709.2:c.693T>A	ENSP00000491912.2:p.Ile231=
ENST00000682296.1:n.1211T>A
ENST00000682550.1:c.1518T>A	ENSP00000507633.1:p.Ile506=
ENST00000682772.1:c.693T>A	ENSP00000506848.1:p.Ile231=
ENST00000682904.1:n.689T>A
ENST00000683029.1:n.281T>A
ENST00000683211.1:c.1863T>A	ENSP00000508257.1:p.Ile621=
ENST00000683250.1:c.*571T>A	ENSP00000506847.1:n.*571T>A
ENST00000683418.1:n.4210T>A
ENST00000684153.1:c.1518T>A	ENSP00000506937.1:p.Ile506=
ENST00000684516.1:n.2882T>A
ENST00000358487.10:c.1869T>A MANE Select	ENSP00000351276.6:p.Ile623=
ENST00000336553.10:c.1596T>A	ENSP00000337665.6:p.Ile532=
ENST00000346997.6:c.1863T>A	ENSP00000263451.5:p.Ile621=
ENST00000351936.10:c.1869T>A	ENSP00000309878.9:p.Ile623=
ENST00000356226.8:c.1518T>A	ENSP00000348559.4:p.Ile506=
ENST00000357555.9:c.1602T>A	ENSP00000350166.5:p.Ile534=
ENST00000358487.9:c.1869T>A	ENSP00000351276.5:p.Ile623=
ENST00000360144.7:c.1605T>A	ENSP00000353262.3:p.Ile535=
ENST00000369056.5:c.1872T>A	ENSP00000358052.1:p.Ile624=
ENST00000369058.7:c.1872T>A	ENSP00000358054.3:p.Ile624=
ENST00000369059.5:c.1527T>A	ENSP00000358055.1:p.Ile509=
ENST00000369060.8:c.1521T>A	ENSP00000358056.4:p.Ile507=
ENST00000369061.8:c.1533T>A	ENSP00000358057.4:p.Ile511=
ENST00000429361.5:c.645T>A	ENSP00000404219.1:p.Ile215=
ENST00000457416.6:c.1872T>A	ENSP00000410294.2:p.Ile624=
ENST00000478859.5:c.1185T>A	ENSP00000474011.1:p.Ile395=
ENST00000604236.5:c.*916T>A	ENSP00000474109.1:n.*916T>A
ENST00000613048.4:c.1602T>A	ENSP00000484154.1:p.Ile534=
NM_000141.4:c.1869T>A	NP_000132.3:p.Ile623=
NM_001144913.1:c.1872T>A	NP_001138385.1:p.Ile624=
NM_001144914.1:c.1533T>A	NP_001138386.1:p.Ile511=
NM_001144915.1:c.1602T>A	NP_001138387.1:p.Ile534=
NM_001144916.1:c.1524T>A	NP_001138388.1:p.Ile508=
NM_001144917.1:c.1521T>A	NP_001138389.1:p.Ile507=
NM_001144918.1:c.1518T>A	NP_001138390.1:p.Ile506=
NM_001144919.1:c.1605T>A	NP_001138391.1:p.Ile535=
NM_022970.3:c.1872T>A	NP_075259.4:p.Ile624=
NM_023029.2:c.1602T>A	NP_075418.1:p.Ile534=
NR_073009.1:n.2319T>A
XM_006717708.2:c.1923T>A	XP_006717771.1:p.Ile641=
XM_006717709.2:c.1920T>A	XP_006717772.1:p.Ile640=
XM_006717710.2:c.1929T>A	XP_006717773.1:p.Ile643=
XM_006717711.2:c.1662T>A	XP_006717774.1:p.Ile554=
XM_006717712.2:c.1584T>A	XP_006717775.1:p.Ile528=
XM_006717713.2:c.1926T>A	XP_006717776.1:p.Ile642=
XM_011539510.1:c.1185T>A	XP_011537812.1:p.Ile395=
NM_001320654.1:c.1185T>A	NP_001307583.1:p.Ile395=
NM_001320658.1:c.1863T>A	NP_001307587.1:p.Ile621=
XM_006717708.3:c.1923T>A	XP_006717771.1:p.Ile641=
XM_006717710.4:c.1929T>A	XP_006717773.1:p.Ile643=
XM_017015920.2:c.1923T>A	XP_016871409.1:p.Ile641=
XM_017015921.2:c.1920T>A	XP_016871410.1:p.Ile640=
XM_017015924.2:c.1581T>A	XP_016871413.1:p.Ile527=
XM_017015925.2:c.1575T>A	XP_016871414.1:p.Ile525=
XM_024447887.1:c.1659T>A	XP_024303655.1:p.Ile553=
XM_024447888.1:c.1656T>A	XP_024303656.1:p.Ile552=
XM_024447889.1:c.1653T>A	XP_024303657.1:p.Ile551=
XM_024447890.1:c.1662T>A	XP_024303658.1:p.Ile554=
XM_024447891.1:c.1584T>A	XP_024303659.1:p.Ile528=
XM_024447892.1:c.699T>A	XP_024303660.1:p.Ile233=
NM_000141.5:c.1869T>A MANE Select	NP_000132.3:p.Ile623=
NM_001144917.2:c.1521T>A	NP_001138389.1:p.Ile507=
NM_001144918.2:c.1518T>A	NP_001138390.1:p.Ile506=
NM_001144919.2:c.1605T>A	NP_001138391.1:p.Ile535=
NM_001320658.2:c.1863T>A	NP_001307587.1:p.Ile621=
NR_073009.2:n.2305T>A
NM_001144915.2:c.1602T>A	NP_001138387.1:p.Ile534=
NM_001144916.2:c.1524T>A	NP_001138388.1:p.Ile508=
NM_001320654.2:c.1185T>A	NP_001307583.1:p.Ile395=