Canonical Allele Identifier: CA471647428

Gene: FGFR2

Linked Data

• MyVariant Identifiers: chr10:g.123247619A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121488105A>G , CM000672.2:g.121488105A>G	GRCh38
NC_000010.10:g.123247619A>G , CM000672.1:g.123247619A>G	GRCh37
NC_000010.9:g.123237609A>G	NCBI36
NG_012449.1:g.115354T>C
NG_012449.2:g.115354T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000457416.7:c.1875T>C MANE Plus Clinical	ENSP00000410294.2:p.His625=
ENST00000351936.11:c.1866T>C	ENSP00000309878.10:p.His622=
ENST00000638709.2:c.696T>C	ENSP00000491912.2:p.His232=
ENST00000682296.1:n.1214T>C
ENST00000682550.1:c.1521T>C	ENSP00000507633.1:p.His507=
ENST00000682772.1:c.696T>C	ENSP00000506848.1:p.His232=
ENST00000682904.1:n.692T>C
ENST00000683029.1:n.284T>C
ENST00000683211.1:c.1866T>C	ENSP00000508257.1:p.His622=
ENST00000683250.1:c.*574T>C	ENSP00000506847.1:n.*574T>C
ENST00000683418.1:n.4213T>C
ENST00000684153.1:c.1521T>C	ENSP00000506937.1:p.His507=
ENST00000684516.1:n.2885T>C
ENST00000358487.10:c.1872T>C MANE Select	ENSP00000351276.6:p.His624=
ENST00000336553.10:c.1599T>C	ENSP00000337665.6:p.His533=
ENST00000346997.6:c.1866T>C	ENSP00000263451.5:p.His622=
ENST00000351936.10:c.1872T>C	ENSP00000309878.9:p.His624=
ENST00000356226.8:c.1521T>C	ENSP00000348559.4:p.His507=
ENST00000357555.9:c.1605T>C	ENSP00000350166.5:p.His535=
ENST00000358487.9:c.1872T>C	ENSP00000351276.5:p.His624=
ENST00000360144.7:c.1608T>C	ENSP00000353262.3:p.His536=
ENST00000369056.5:c.1875T>C	ENSP00000358052.1:p.His625=
ENST00000369058.7:c.1875T>C	ENSP00000358054.3:p.His625=
ENST00000369059.5:c.1530T>C	ENSP00000358055.1:p.His510=
ENST00000369060.8:c.1524T>C	ENSP00000358056.4:p.His508=
ENST00000369061.8:c.1536T>C	ENSP00000358057.4:p.His512=
ENST00000429361.5:c.648T>C	ENSP00000404219.1:p.His216=
ENST00000457416.6:c.1875T>C	ENSP00000410294.2:p.His625=
ENST00000478859.5:c.1188T>C	ENSP00000474011.1:p.His396=
ENST00000604236.5:c.*919T>C	ENSP00000474109.1:n.*919T>C
ENST00000613048.4:c.1605T>C	ENSP00000484154.1:p.His535=
NM_000141.4:c.1872T>C	NP_000132.3:p.His624=
NM_001144913.1:c.1875T>C	NP_001138385.1:p.His625=
NM_001144914.1:c.1536T>C	NP_001138386.1:p.His512=
NM_001144915.1:c.1605T>C	NP_001138387.1:p.His535=
NM_001144916.1:c.1527T>C	NP_001138388.1:p.His509=
NM_001144917.1:c.1524T>C	NP_001138389.1:p.His508=
NM_001144918.1:c.1521T>C	NP_001138390.1:p.His507=
NM_001144919.1:c.1608T>C	NP_001138391.1:p.His536=
NM_022970.3:c.1875T>C	NP_075259.4:p.His625=
NM_023029.2:c.1605T>C	NP_075418.1:p.His535=
NR_073009.1:n.2322T>C
XM_006717708.2:c.1926T>C	XP_006717771.1:p.His642=
XM_006717709.2:c.1923T>C	XP_006717772.1:p.His641=
XM_006717710.2:c.1932T>C	XP_006717773.1:p.His644=
XM_006717711.2:c.1665T>C	XP_006717774.1:p.His555=
XM_006717712.2:c.1587T>C	XP_006717775.1:p.His529=
XM_006717713.2:c.1929T>C	XP_006717776.1:p.His643=
XM_011539510.1:c.1188T>C	XP_011537812.1:p.His396=
NM_001320654.1:c.1188T>C	NP_001307583.1:p.His396=
NM_001320658.1:c.1866T>C	NP_001307587.1:p.His622=
XM_006717708.3:c.1926T>C	XP_006717771.1:p.His642=
XM_006717710.4:c.1932T>C	XP_006717773.1:p.His644=
XM_017015920.2:c.1926T>C	XP_016871409.1:p.His642=
XM_017015921.2:c.1923T>C	XP_016871410.1:p.His641=
XM_017015924.2:c.1584T>C	XP_016871413.1:p.His528=
XM_017015925.2:c.1578T>C	XP_016871414.1:p.His526=
XM_024447887.1:c.1662T>C	XP_024303655.1:p.His554=
XM_024447888.1:c.1659T>C	XP_024303656.1:p.His553=
XM_024447889.1:c.1656T>C	XP_024303657.1:p.His552=
XM_024447890.1:c.1665T>C	XP_024303658.1:p.His555=
XM_024447891.1:c.1587T>C	XP_024303659.1:p.His529=
XM_024447892.1:c.702T>C	XP_024303660.1:p.His234=
NM_000141.5:c.1872T>C MANE Select	NP_000132.3:p.His624=
NM_001144917.2:c.1524T>C	NP_001138389.1:p.His508=
NM_001144918.2:c.1521T>C	NP_001138390.1:p.His507=
NM_001144919.2:c.1608T>C	NP_001138391.1:p.His536=
NM_001320658.2:c.1866T>C	NP_001307587.1:p.His622=
NR_073009.2:n.2308T>C
NM_001144915.2:c.1605T>C	NP_001138387.1:p.His535=
NM_001144916.2:c.1527T>C	NP_001138388.1:p.His509=
NM_001320654.2:c.1188T>C	NP_001307583.1:p.His396=