Canonical Allele Identifier: CA378314082

Gene: FGFR2

Linked Data

• dbSNP Id: rs2133834644
• MyVariant Identifiers: chr10:g.123247512G>C (hg19) ; chr10:g.121487998G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121487998G>C , CM000672.2:g.121487998G>C	GRCh38
NC_000010.10:g.123247512G>C , CM000672.1:g.123247512G>C	GRCh37
NC_000010.9:g.123237502G>C	NCBI36
NG_012449.1:g.115461C>G
NG_012449.2:g.115461C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000457416.7:c.1982C>G MANE Plus Clinical	ENSP00000410294.2:p.Thr661Ser
ENST00000351936.11:c.1973C>G	ENSP00000309878.10:p.Thr658Ser
ENST00000638709.2:c.803C>G	ENSP00000491912.2:p.Thr268Ser
ENST00000682296.1:n.1321C>G
ENST00000682550.1:c.1628C>G	ENSP00000507633.1:p.Thr543Ser
ENST00000682772.1:c.803C>G	ENSP00000506848.1:p.Thr268Ser
ENST00000682904.1:n.799C>G
ENST00000683029.1:n.391C>G
ENST00000683211.1:c.1973C>G	ENSP00000508257.1:p.Thr658Ser
ENST00000683250.1:c.*681C>G	ENSP00000506847.1:n.*681C>G
ENST00000683418.1:n.4320C>G
ENST00000684153.1:c.1628C>G	ENSP00000506937.1:p.Thr543Ser
ENST00000684516.1:n.2992C>G
ENST00000358487.10:c.1979C>G MANE Select	ENSP00000351276.6:p.Thr660Ser
ENST00000336553.10:c.1706C>G	ENSP00000337665.6:p.Thr569Ser
ENST00000346997.6:c.1973C>G	ENSP00000263451.5:p.Thr658Ser
ENST00000351936.10:c.1979C>G	ENSP00000309878.9:p.Thr660Ser
ENST00000356226.8:c.1628C>G	ENSP00000348559.4:p.Thr543Ser
ENST00000357555.9:c.1712C>G	ENSP00000350166.5:p.Thr571Ser
ENST00000358487.9:c.1979C>G	ENSP00000351276.5:p.Thr660Ser
ENST00000360144.7:c.1715C>G	ENSP00000353262.3:p.Thr572Ser
ENST00000369056.5:c.1982C>G	ENSP00000358052.1:p.Thr661Ser
ENST00000369058.7:c.1982C>G	ENSP00000358054.3:p.Thr661Ser
ENST00000369059.5:c.1637C>G	ENSP00000358055.1:p.Thr546Ser
ENST00000369060.8:c.1631C>G	ENSP00000358056.4:p.Thr544Ser
ENST00000369061.8:c.1643C>G	ENSP00000358057.4:p.Thr548Ser
ENST00000429361.5:c.755C>G	ENSP00000404219.1:p.Thr252Ser
ENST00000457416.6:c.1982C>G	ENSP00000410294.2:p.Thr661Ser
ENST00000478859.5:c.1295C>G	ENSP00000474011.1:p.Thr432Ser
ENST00000604236.5:c.*1026C>G	ENSP00000474109.1:n.*1026C>G
ENST00000613048.4:c.1712C>G	ENSP00000484154.1:p.Thr571Ser
NM_000141.4:c.1979C>G	NP_000132.3:p.Thr660Ser
NM_001144913.1:c.1982C>G	NP_001138385.1:p.Thr661Ser
NM_001144914.1:c.1643C>G	NP_001138386.1:p.Thr548Ser
NM_001144915.1:c.1712C>G	NP_001138387.1:p.Thr571Ser
NM_001144916.1:c.1634C>G	NP_001138388.1:p.Thr545Ser
NM_001144917.1:c.1631C>G	NP_001138389.1:p.Thr544Ser
NM_001144918.1:c.1628C>G	NP_001138390.1:p.Thr543Ser
NM_001144919.1:c.1715C>G	NP_001138391.1:p.Thr572Ser
NM_022970.3:c.1982C>G	NP_075259.4:p.Thr661Ser
NM_023029.2:c.1712C>G	NP_075418.1:p.Thr571Ser
NR_073009.1:n.2429C>G
XM_006717708.2:c.2033C>G	XP_006717771.1:p.Thr678Ser
XM_006717709.2:c.2030C>G	XP_006717772.1:p.Thr677Ser
XM_006717710.2:c.2039C>G	XP_006717773.1:p.Thr680Ser
XM_006717711.2:c.1772C>G	XP_006717774.1:p.Thr591Ser
XM_006717712.2:c.1694C>G	XP_006717775.1:p.Thr565Ser
XM_006717713.2:c.2036C>G	XP_006717776.1:p.Thr679Ser
XM_011539510.1:c.1295C>G	XP_011537812.1:p.Thr432Ser
NM_001320654.1:c.1295C>G	NP_001307583.1:p.Thr432Ser
NM_001320658.1:c.1973C>G	NP_001307587.1:p.Thr658Ser
XM_006717708.3:c.2033C>G	XP_006717771.1:p.Thr678Ser
XM_006717710.4:c.2039C>G	XP_006717773.1:p.Thr680Ser
XM_017015920.2:c.2033C>G	XP_016871409.1:p.Thr678Ser
XM_017015921.2:c.2030C>G	XP_016871410.1:p.Thr677Ser
XM_017015924.2:c.1691C>G	XP_016871413.1:p.Thr564Ser
XM_017015925.2:c.1685C>G	XP_016871414.1:p.Thr562Ser
XM_024447887.1:c.1769C>G	XP_024303655.1:p.Thr590Ser
XM_024447888.1:c.1766C>G	XP_024303656.1:p.Thr589Ser
XM_024447889.1:c.1763C>G	XP_024303657.1:p.Thr588Ser
XM_024447890.1:c.1772C>G	XP_024303658.1:p.Thr591Ser
XM_024447891.1:c.1694C>G	XP_024303659.1:p.Thr565Ser
XM_024447892.1:c.809C>G	XP_024303660.1:p.Thr270Ser
NM_000141.5:c.1979C>G MANE Select	NP_000132.3:p.Thr660Ser
NM_001144917.2:c.1631C>G	NP_001138389.1:p.Thr544Ser
NM_001144918.2:c.1628C>G	NP_001138390.1:p.Thr543Ser
NM_001144919.2:c.1715C>G	NP_001138391.1:p.Thr572Ser
NM_001320658.2:c.1973C>G	NP_001307587.1:p.Thr658Ser
NR_073009.2:n.2415C>G
NM_001144915.2:c.1712C>G	NP_001138387.1:p.Thr571Ser
NM_001144916.2:c.1634C>G	NP_001138388.1:p.Thr545Ser
NM_001320654.2:c.1295C>G	NP_001307583.1:p.Thr432Ser