Canonical Allele Identifier: CA471647420

Gene: FGFR2

Linked Data

• MyVariant Identifiers: chr10:g.123247616T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121488102T>C , CM000672.2:g.121488102T>C	GRCh38
NC_000010.10:g.123247616T>C , CM000672.1:g.123247616T>C	GRCh37
NC_000010.9:g.123237606T>C	NCBI36
NG_012449.1:g.115357A>G
NG_012449.2:g.115357A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000457416.7:c.1878A>G MANE Plus Clinical	ENSP00000410294.2:p.Arg626=
ENST00000351936.11:c.1869A>G	ENSP00000309878.10:p.Arg623=
ENST00000638709.2:c.699A>G	ENSP00000491912.2:p.Arg233=
ENST00000682296.1:n.1217A>G
ENST00000682550.1:c.1524A>G	ENSP00000507633.1:p.Arg508=
ENST00000682772.1:c.699A>G	ENSP00000506848.1:p.Arg233=
ENST00000682904.1:n.695A>G
ENST00000683029.1:n.287A>G
ENST00000683211.1:c.1869A>G	ENSP00000508257.1:p.Arg623=
ENST00000683250.1:c.*577A>G	ENSP00000506847.1:n.*577A>G
ENST00000683418.1:n.4216A>G
ENST00000684153.1:c.1524A>G	ENSP00000506937.1:p.Arg508=
ENST00000684516.1:n.2888A>G
ENST00000358487.10:c.1875A>G MANE Select	ENSP00000351276.6:p.Arg625=
ENST00000336553.10:c.1602A>G	ENSP00000337665.6:p.Arg534=
ENST00000346997.6:c.1869A>G	ENSP00000263451.5:p.Arg623=
ENST00000351936.10:c.1875A>G	ENSP00000309878.9:p.Arg625=
ENST00000356226.8:c.1524A>G	ENSP00000348559.4:p.Arg508=
ENST00000357555.9:c.1608A>G	ENSP00000350166.5:p.Arg536=
ENST00000358487.9:c.1875A>G	ENSP00000351276.5:p.Arg625=
ENST00000360144.7:c.1611A>G	ENSP00000353262.3:p.Arg537=
ENST00000369056.5:c.1878A>G	ENSP00000358052.1:p.Arg626=
ENST00000369058.7:c.1878A>G	ENSP00000358054.3:p.Arg626=
ENST00000369059.5:c.1533A>G	ENSP00000358055.1:p.Arg511=
ENST00000369060.8:c.1527A>G	ENSP00000358056.4:p.Arg509=
ENST00000369061.8:c.1539A>G	ENSP00000358057.4:p.Arg513=
ENST00000429361.5:c.651A>G	ENSP00000404219.1:p.Arg217=
ENST00000457416.6:c.1878A>G	ENSP00000410294.2:p.Arg626=
ENST00000478859.5:c.1191A>G	ENSP00000474011.1:p.Arg397=
ENST00000604236.5:c.*922A>G	ENSP00000474109.1:n.*922A>G
ENST00000613048.4:c.1608A>G	ENSP00000484154.1:p.Arg536=
NM_000141.4:c.1875A>G	NP_000132.3:p.Arg625=
NM_001144913.1:c.1878A>G	NP_001138385.1:p.Arg626=
NM_001144914.1:c.1539A>G	NP_001138386.1:p.Arg513=
NM_001144915.1:c.1608A>G	NP_001138387.1:p.Arg536=
NM_001144916.1:c.1530A>G	NP_001138388.1:p.Arg510=
NM_001144917.1:c.1527A>G	NP_001138389.1:p.Arg509=
NM_001144918.1:c.1524A>G	NP_001138390.1:p.Arg508=
NM_001144919.1:c.1611A>G	NP_001138391.1:p.Arg537=
NM_022970.3:c.1878A>G	NP_075259.4:p.Arg626=
NM_023029.2:c.1608A>G	NP_075418.1:p.Arg536=
NR_073009.1:n.2325A>G
XM_006717708.2:c.1929A>G	XP_006717771.1:p.Arg643=
XM_006717709.2:c.1926A>G	XP_006717772.1:p.Arg642=
XM_006717710.2:c.1935A>G	XP_006717773.1:p.Arg645=
XM_006717711.2:c.1668A>G	XP_006717774.1:p.Arg556=
XM_006717712.2:c.1590A>G	XP_006717775.1:p.Arg530=
XM_006717713.2:c.1932A>G	XP_006717776.1:p.Arg644=
XM_011539510.1:c.1191A>G	XP_011537812.1:p.Arg397=
NM_001320654.1:c.1191A>G	NP_001307583.1:p.Arg397=
NM_001320658.1:c.1869A>G	NP_001307587.1:p.Arg623=
XM_006717708.3:c.1929A>G	XP_006717771.1:p.Arg643=
XM_006717710.4:c.1935A>G	XP_006717773.1:p.Arg645=
XM_017015920.2:c.1929A>G	XP_016871409.1:p.Arg643=
XM_017015921.2:c.1926A>G	XP_016871410.1:p.Arg642=
XM_017015924.2:c.1587A>G	XP_016871413.1:p.Arg529=
XM_017015925.2:c.1581A>G	XP_016871414.1:p.Arg527=
XM_024447887.1:c.1665A>G	XP_024303655.1:p.Arg555=
XM_024447888.1:c.1662A>G	XP_024303656.1:p.Arg554=
XM_024447889.1:c.1659A>G	XP_024303657.1:p.Arg553=
XM_024447890.1:c.1668A>G	XP_024303658.1:p.Arg556=
XM_024447891.1:c.1590A>G	XP_024303659.1:p.Arg530=
XM_024447892.1:c.705A>G	XP_024303660.1:p.Arg235=
NM_000141.5:c.1875A>G MANE Select	NP_000132.3:p.Arg625=
NM_001144917.2:c.1527A>G	NP_001138389.1:p.Arg509=
NM_001144918.2:c.1524A>G	NP_001138390.1:p.Arg508=
NM_001144919.2:c.1611A>G	NP_001138391.1:p.Arg537=
NM_001320658.2:c.1869A>G	NP_001307587.1:p.Arg623=
NR_073009.2:n.2311A>G
NM_001144915.2:c.1608A>G	NP_001138387.1:p.Arg536=
NM_001144916.2:c.1530A>G	NP_001138388.1:p.Arg510=
NM_001320654.2:c.1191A>G	NP_001307583.1:p.Arg397=