Canonical Allele Identifier: CA378314946

Gene: FGFR2

Linked Data

• dbSNP Id: rs2133838768
• MyVariant Identifiers: chr10:g.123247602C>T (hg19) ; chr10:g.121488088C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121488088C>T , CM000672.2:g.121488088C>T	GRCh38
NC_000010.10:g.123247602C>T , CM000672.1:g.123247602C>T	GRCh37
NC_000010.9:g.123237592C>T	NCBI36
NG_012449.1:g.115371G>A
NG_012449.2:g.115371G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000457416.7:c.1892G>A MANE Plus Clinical	ENSP00000410294.2:p.Arg631Lys
ENST00000351936.11:c.1883G>A	ENSP00000309878.10:p.Arg628Lys
ENST00000638709.2:c.713G>A	ENSP00000491912.2:p.Arg238Lys
ENST00000682296.1:n.1231G>A
ENST00000682550.1:c.1538G>A	ENSP00000507633.1:p.Arg513Lys
ENST00000682772.1:c.713G>A	ENSP00000506848.1:p.Arg238Lys
ENST00000682904.1:n.709G>A
ENST00000683029.1:n.301G>A
ENST00000683211.1:c.1883G>A	ENSP00000508257.1:p.Arg628Lys
ENST00000683250.1:c.*591G>A	ENSP00000506847.1:n.*591G>A
ENST00000683418.1:n.4230G>A
ENST00000684153.1:c.1538G>A	ENSP00000506937.1:p.Arg513Lys
ENST00000684516.1:n.2902G>A
ENST00000358487.10:c.1889G>A MANE Select	ENSP00000351276.6:p.Arg630Lys
ENST00000336553.10:c.1616G>A	ENSP00000337665.6:p.Arg539Lys
ENST00000346997.6:c.1883G>A	ENSP00000263451.5:p.Arg628Lys
ENST00000351936.10:c.1889G>A	ENSP00000309878.9:p.Arg630Lys
ENST00000356226.8:c.1538G>A	ENSP00000348559.4:p.Arg513Lys
ENST00000357555.9:c.1622G>A	ENSP00000350166.5:p.Arg541Lys
ENST00000358487.9:c.1889G>A	ENSP00000351276.5:p.Arg630Lys
ENST00000360144.7:c.1625G>A	ENSP00000353262.3:p.Arg542Lys
ENST00000369056.5:c.1892G>A	ENSP00000358052.1:p.Arg631Lys
ENST00000369058.7:c.1892G>A	ENSP00000358054.3:p.Arg631Lys
ENST00000369059.5:c.1547G>A	ENSP00000358055.1:p.Arg516Lys
ENST00000369060.8:c.1541G>A	ENSP00000358056.4:p.Arg514Lys
ENST00000369061.8:c.1553G>A	ENSP00000358057.4:p.Arg518Lys
ENST00000429361.5:c.665G>A	ENSP00000404219.1:p.Arg222Lys
ENST00000457416.6:c.1892G>A	ENSP00000410294.2:p.Arg631Lys
ENST00000478859.5:c.1205G>A	ENSP00000474011.1:p.Arg402Lys
ENST00000604236.5:c.*936G>A	ENSP00000474109.1:n.*936G>A
ENST00000613048.4:c.1622G>A	ENSP00000484154.1:p.Arg541Lys
NM_000141.4:c.1889G>A	NP_000132.3:p.Arg630Lys
NM_001144913.1:c.1892G>A	NP_001138385.1:p.Arg631Lys
NM_001144914.1:c.1553G>A	NP_001138386.1:p.Arg518Lys
NM_001144915.1:c.1622G>A	NP_001138387.1:p.Arg541Lys
NM_001144916.1:c.1544G>A	NP_001138388.1:p.Arg515Lys
NM_001144917.1:c.1541G>A	NP_001138389.1:p.Arg514Lys
NM_001144918.1:c.1538G>A	NP_001138390.1:p.Arg513Lys
NM_001144919.1:c.1625G>A	NP_001138391.1:p.Arg542Lys
NM_022970.3:c.1892G>A	NP_075259.4:p.Arg631Lys
NM_023029.2:c.1622G>A	NP_075418.1:p.Arg541Lys
NR_073009.1:n.2339G>A
XM_006717708.2:c.1943G>A	XP_006717771.1:p.Arg648Lys
XM_006717709.2:c.1940G>A	XP_006717772.1:p.Arg647Lys
XM_006717710.2:c.1949G>A	XP_006717773.1:p.Arg650Lys
XM_006717711.2:c.1682G>A	XP_006717774.1:p.Arg561Lys
XM_006717712.2:c.1604G>A	XP_006717775.1:p.Arg535Lys
XM_006717713.2:c.1946G>A	XP_006717776.1:p.Arg649Lys
XM_011539510.1:c.1205G>A	XP_011537812.1:p.Arg402Lys
NM_001320654.1:c.1205G>A	NP_001307583.1:p.Arg402Lys
NM_001320658.1:c.1883G>A	NP_001307587.1:p.Arg628Lys
XM_006717708.3:c.1943G>A	XP_006717771.1:p.Arg648Lys
XM_006717710.4:c.1949G>A	XP_006717773.1:p.Arg650Lys
XM_017015920.2:c.1943G>A	XP_016871409.1:p.Arg648Lys
XM_017015921.2:c.1940G>A	XP_016871410.1:p.Arg647Lys
XM_017015924.2:c.1601G>A	XP_016871413.1:p.Arg534Lys
XM_017015925.2:c.1595G>A	XP_016871414.1:p.Arg532Lys
XM_024447887.1:c.1679G>A	XP_024303655.1:p.Arg560Lys
XM_024447888.1:c.1676G>A	XP_024303656.1:p.Arg559Lys
XM_024447889.1:c.1673G>A	XP_024303657.1:p.Arg558Lys
XM_024447890.1:c.1682G>A	XP_024303658.1:p.Arg561Lys
XM_024447891.1:c.1604G>A	XP_024303659.1:p.Arg535Lys
XM_024447892.1:c.719G>A	XP_024303660.1:p.Arg240Lys
NM_000141.5:c.1889G>A MANE Select	NP_000132.3:p.Arg630Lys
NM_001144917.2:c.1541G>A	NP_001138389.1:p.Arg514Lys
NM_001144918.2:c.1538G>A	NP_001138390.1:p.Arg513Lys
NM_001144919.2:c.1625G>A	NP_001138391.1:p.Arg542Lys
NM_001320658.2:c.1883G>A	NP_001307587.1:p.Arg628Lys
NR_073009.2:n.2325G>A
NM_001144915.2:c.1622G>A	NP_001138387.1:p.Arg541Lys
NM_001144916.2:c.1544G>A	NP_001138388.1:p.Arg515Lys
NM_001320654.2:c.1205G>A	NP_001307583.1:p.Arg402Lys