Canonical Allele Identifier: CA471647413

Gene: FGFR2

Linked Data

• MyVariant Identifiers: chr10:g.123247613A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121488099A>G , CM000672.2:g.121488099A>G	GRCh38
NC_000010.10:g.123247613A>G , CM000672.1:g.123247613A>G	GRCh37
NC_000010.9:g.123237603A>G	NCBI36
NG_012449.1:g.115360T>C
NG_012449.2:g.115360T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000457416.7:c.1881T>C MANE Plus Clinical	ENSP00000410294.2:p.Asp627=
ENST00000351936.11:c.1872T>C	ENSP00000309878.10:p.Asp624=
ENST00000638709.2:c.702T>C	ENSP00000491912.2:p.Asp234=
ENST00000682296.1:n.1220T>C
ENST00000682550.1:c.1527T>C	ENSP00000507633.1:p.Asp509=
ENST00000682772.1:c.702T>C	ENSP00000506848.1:p.Asp234=
ENST00000682904.1:n.698T>C
ENST00000683029.1:n.290T>C
ENST00000683211.1:c.1872T>C	ENSP00000508257.1:p.Asp624=
ENST00000683250.1:c.*580T>C	ENSP00000506847.1:n.*580T>C
ENST00000683418.1:n.4219T>C
ENST00000684153.1:c.1527T>C	ENSP00000506937.1:p.Asp509=
ENST00000684516.1:n.2891T>C
ENST00000358487.10:c.1878T>C MANE Select	ENSP00000351276.6:p.Asp626=
ENST00000336553.10:c.1605T>C	ENSP00000337665.6:p.Asp535=
ENST00000346997.6:c.1872T>C	ENSP00000263451.5:p.Asp624=
ENST00000351936.10:c.1878T>C	ENSP00000309878.9:p.Asp626=
ENST00000356226.8:c.1527T>C	ENSP00000348559.4:p.Asp509=
ENST00000357555.9:c.1611T>C	ENSP00000350166.5:p.Asp537=
ENST00000358487.9:c.1878T>C	ENSP00000351276.5:p.Asp626=
ENST00000360144.7:c.1614T>C	ENSP00000353262.3:p.Asp538=
ENST00000369056.5:c.1881T>C	ENSP00000358052.1:p.Asp627=
ENST00000369058.7:c.1881T>C	ENSP00000358054.3:p.Asp627=
ENST00000369059.5:c.1536T>C	ENSP00000358055.1:p.Asp512=
ENST00000369060.8:c.1530T>C	ENSP00000358056.4:p.Asp510=
ENST00000369061.8:c.1542T>C	ENSP00000358057.4:p.Asp514=
ENST00000429361.5:c.654T>C	ENSP00000404219.1:p.Asp218=
ENST00000457416.6:c.1881T>C	ENSP00000410294.2:p.Asp627=
ENST00000478859.5:c.1194T>C	ENSP00000474011.1:p.Asp398=
ENST00000604236.5:c.*925T>C	ENSP00000474109.1:n.*925T>C
ENST00000613048.4:c.1611T>C	ENSP00000484154.1:p.Asp537=
NM_000141.4:c.1878T>C	NP_000132.3:p.Asp626=
NM_001144913.1:c.1881T>C	NP_001138385.1:p.Asp627=
NM_001144914.1:c.1542T>C	NP_001138386.1:p.Asp514=
NM_001144915.1:c.1611T>C	NP_001138387.1:p.Asp537=
NM_001144916.1:c.1533T>C	NP_001138388.1:p.Asp511=
NM_001144917.1:c.1530T>C	NP_001138389.1:p.Asp510=
NM_001144918.1:c.1527T>C	NP_001138390.1:p.Asp509=
NM_001144919.1:c.1614T>C	NP_001138391.1:p.Asp538=
NM_022970.3:c.1881T>C	NP_075259.4:p.Asp627=
NM_023029.2:c.1611T>C	NP_075418.1:p.Asp537=
NR_073009.1:n.2328T>C
XM_006717708.2:c.1932T>C	XP_006717771.1:p.Asp644=
XM_006717709.2:c.1929T>C	XP_006717772.1:p.Asp643=
XM_006717710.2:c.1938T>C	XP_006717773.1:p.Asp646=
XM_006717711.2:c.1671T>C	XP_006717774.1:p.Asp557=
XM_006717712.2:c.1593T>C	XP_006717775.1:p.Asp531=
XM_006717713.2:c.1935T>C	XP_006717776.1:p.Asp645=
XM_011539510.1:c.1194T>C	XP_011537812.1:p.Asp398=
NM_001320654.1:c.1194T>C	NP_001307583.1:p.Asp398=
NM_001320658.1:c.1872T>C	NP_001307587.1:p.Asp624=
XM_006717708.3:c.1932T>C	XP_006717771.1:p.Asp644=
XM_006717710.4:c.1938T>C	XP_006717773.1:p.Asp646=
XM_017015920.2:c.1932T>C	XP_016871409.1:p.Asp644=
XM_017015921.2:c.1929T>C	XP_016871410.1:p.Asp643=
XM_017015924.2:c.1590T>C	XP_016871413.1:p.Asp530=
XM_017015925.2:c.1584T>C	XP_016871414.1:p.Asp528=
XM_024447887.1:c.1668T>C	XP_024303655.1:p.Asp556=
XM_024447888.1:c.1665T>C	XP_024303656.1:p.Asp555=
XM_024447889.1:c.1662T>C	XP_024303657.1:p.Asp554=
XM_024447890.1:c.1671T>C	XP_024303658.1:p.Asp557=
XM_024447891.1:c.1593T>C	XP_024303659.1:p.Asp531=
XM_024447892.1:c.708T>C	XP_024303660.1:p.Asp236=
NM_000141.5:c.1878T>C MANE Select	NP_000132.3:p.Asp626=
NM_001144917.2:c.1530T>C	NP_001138389.1:p.Asp510=
NM_001144918.2:c.1527T>C	NP_001138390.1:p.Asp509=
NM_001144919.2:c.1614T>C	NP_001138391.1:p.Asp538=
NM_001320658.2:c.1872T>C	NP_001307587.1:p.Asp624=
NR_073009.2:n.2314T>C
NM_001144915.2:c.1611T>C	NP_001138387.1:p.Asp537=
NM_001144916.2:c.1533T>C	NP_001138388.1:p.Asp511=
NM_001320654.2:c.1194T>C	NP_001307583.1:p.Asp398=