Canonical Allele Identifier: CA378314609

Gene: FGFR2

Linked Data

• MyVariant Identifiers: chr10:g.123247558A>T (hg19) ; chr10:g.121488044A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121488044A>T , CM000672.2:g.121488044A>T	GRCh38
NC_000010.10:g.123247558A>T , CM000672.1:g.123247558A>T	GRCh37
NC_000010.9:g.123237548A>T	NCBI36
NG_012449.1:g.115415T>A
NG_012449.2:g.115415T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000457416.7:c.1936T>A MANE Plus Clinical	ENSP00000410294.2:p.Phe646Ile
ENST00000351936.11:c.1927T>A	ENSP00000309878.10:p.Phe643Ile
ENST00000638709.2:c.757T>A	ENSP00000491912.2:p.Phe253Ile
ENST00000682296.1:n.1275T>A
ENST00000682550.1:c.1582T>A	ENSP00000507633.1:p.Phe528Ile
ENST00000682772.1:c.757T>A	ENSP00000506848.1:p.Phe253Ile
ENST00000682904.1:n.753T>A
ENST00000683029.1:n.345T>A
ENST00000683211.1:c.1927T>A	ENSP00000508257.1:p.Phe643Ile
ENST00000683250.1:c.*635T>A	ENSP00000506847.1:n.*635T>A
ENST00000683418.1:n.4274T>A
ENST00000684153.1:c.1582T>A	ENSP00000506937.1:p.Phe528Ile
ENST00000684516.1:n.2946T>A
ENST00000358487.10:c.1933T>A MANE Select	ENSP00000351276.6:p.Phe645Ile
ENST00000336553.10:c.1660T>A	ENSP00000337665.6:p.Phe554Ile
ENST00000346997.6:c.1927T>A	ENSP00000263451.5:p.Phe643Ile
ENST00000351936.10:c.1933T>A	ENSP00000309878.9:p.Phe645Ile
ENST00000356226.8:c.1582T>A	ENSP00000348559.4:p.Phe528Ile
ENST00000357555.9:c.1666T>A	ENSP00000350166.5:p.Phe556Ile
ENST00000358487.9:c.1933T>A	ENSP00000351276.5:p.Phe645Ile
ENST00000360144.7:c.1669T>A	ENSP00000353262.3:p.Phe557Ile
ENST00000369056.5:c.1936T>A	ENSP00000358052.1:p.Phe646Ile
ENST00000369058.7:c.1936T>A	ENSP00000358054.3:p.Phe646Ile
ENST00000369059.5:c.1591T>A	ENSP00000358055.1:p.Phe531Ile
ENST00000369060.8:c.1585T>A	ENSP00000358056.4:p.Phe529Ile
ENST00000369061.8:c.1597T>A	ENSP00000358057.4:p.Phe533Ile
ENST00000429361.5:c.709T>A	ENSP00000404219.1:p.Phe237Ile
ENST00000457416.6:c.1936T>A	ENSP00000410294.2:p.Phe646Ile
ENST00000478859.5:c.1249T>A	ENSP00000474011.1:p.Phe417Ile
ENST00000604236.5:c.*980T>A	ENSP00000474109.1:n.*980T>A
ENST00000613048.4:c.1666T>A	ENSP00000484154.1:p.Phe556Ile
NM_000141.4:c.1933T>A	NP_000132.3:p.Phe645Ile
NM_001144913.1:c.1936T>A	NP_001138385.1:p.Phe646Ile
NM_001144914.1:c.1597T>A	NP_001138386.1:p.Phe533Ile
NM_001144915.1:c.1666T>A	NP_001138387.1:p.Phe556Ile
NM_001144916.1:c.1588T>A	NP_001138388.1:p.Phe530Ile
NM_001144917.1:c.1585T>A	NP_001138389.1:p.Phe529Ile
NM_001144918.1:c.1582T>A	NP_001138390.1:p.Phe528Ile
NM_001144919.1:c.1669T>A	NP_001138391.1:p.Phe557Ile
NM_022970.3:c.1936T>A	NP_075259.4:p.Phe646Ile
NM_023029.2:c.1666T>A	NP_075418.1:p.Phe556Ile
NR_073009.1:n.2383T>A
XM_006717708.2:c.1987T>A	XP_006717771.1:p.Phe663Ile
XM_006717709.2:c.1984T>A	XP_006717772.1:p.Phe662Ile
XM_006717710.2:c.1993T>A	XP_006717773.1:p.Phe665Ile
XM_006717711.2:c.1726T>A	XP_006717774.1:p.Phe576Ile
XM_006717712.2:c.1648T>A	XP_006717775.1:p.Phe550Ile
XM_006717713.2:c.1990T>A	XP_006717776.1:p.Phe664Ile
XM_011539510.1:c.1249T>A	XP_011537812.1:p.Phe417Ile
NM_001320654.1:c.1249T>A	NP_001307583.1:p.Phe417Ile
NM_001320658.1:c.1927T>A	NP_001307587.1:p.Phe643Ile
XM_006717708.3:c.1987T>A	XP_006717771.1:p.Phe663Ile
XM_006717710.4:c.1993T>A	XP_006717773.1:p.Phe665Ile
XM_017015920.2:c.1987T>A	XP_016871409.1:p.Phe663Ile
XM_017015921.2:c.1984T>A	XP_016871410.1:p.Phe662Ile
XM_017015924.2:c.1645T>A	XP_016871413.1:p.Phe549Ile
XM_017015925.2:c.1639T>A	XP_016871414.1:p.Phe547Ile
XM_024447887.1:c.1723T>A	XP_024303655.1:p.Phe575Ile
XM_024447888.1:c.1720T>A	XP_024303656.1:p.Phe574Ile
XM_024447889.1:c.1717T>A	XP_024303657.1:p.Phe573Ile
XM_024447890.1:c.1726T>A	XP_024303658.1:p.Phe576Ile
XM_024447891.1:c.1648T>A	XP_024303659.1:p.Phe550Ile
XM_024447892.1:c.763T>A	XP_024303660.1:p.Phe255Ile
NM_000141.5:c.1933T>A MANE Select	NP_000132.3:p.Phe645Ile
NM_001144917.2:c.1585T>A	NP_001138389.1:p.Phe529Ile
NM_001144918.2:c.1582T>A	NP_001138390.1:p.Phe528Ile
NM_001144919.2:c.1669T>A	NP_001138391.1:p.Phe557Ile
NM_001320658.2:c.1927T>A	NP_001307587.1:p.Phe643Ile
NR_073009.2:n.2369T>A
NM_001144915.2:c.1666T>A	NP_001138387.1:p.Phe556Ile
NM_001144916.2:c.1588T>A	NP_001138388.1:p.Phe530Ile
NM_001320654.2:c.1249T>A	NP_001307583.1:p.Phe417Ile