Canonical Allele Identifier: CA378320383

Gene: FGFR2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121496660G>A , CM000672.2:g.121496660G>A	GRCh38
NC_000010.10:g.123256174G>A , CM000672.1:g.123256174G>A	GRCh37
NC_000010.9:g.123246164G>A	NCBI36
NG_012449.1:g.106799C>T
NG_012449.2:g.106799C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000457416.7:c.1738C>T MANE Plus Clinical	ENSP00000410294.2:p.Arg580Trp
ENST00000351936.11:c.1729C>T	ENSP00000309878.10:p.Arg577Trp
ENST00000638709.2:c.559C>T	ENSP00000491912.2:p.Arg187Trp
ENST00000682296.1:n.1077C>T
ENST00000682550.1:c.1384C>T	ENSP00000507633.1:p.Arg462Trp
ENST00000682772.1:c.559C>T	ENSP00000506848.1:p.Arg187Trp
ENST00000682904.1:n.555C>T
ENST00000683029.1:n.147C>T
ENST00000683211.1:c.1729C>T	ENSP00000508257.1:p.Arg577Trp
ENST00000683250.1:c.*437C>T	ENSP00000506847.1:n.*437C>T
ENST00000683418.1:n.4076C>T
ENST00000684153.1:c.1384C>T	ENSP00000506937.1:p.Arg462Trp
ENST00000684516.1:n.2748C>T
ENST00000358487.10:c.1735C>T MANE Select	ENSP00000351276.6:p.Arg579Trp
ENST00000336553.10:c.1462C>T	ENSP00000337665.6:p.Arg488Trp
ENST00000346997.6:c.1729C>T	ENSP00000263451.5:p.Arg577Trp
ENST00000351936.10:c.1735C>T	ENSP00000309878.9:p.Arg579Trp
ENST00000356226.8:c.1384C>T	ENSP00000348559.4:p.Arg462Trp
ENST00000357555.9:c.1468C>T	ENSP00000350166.5:p.Arg490Trp
ENST00000358487.9:c.1735C>T	ENSP00000351276.5:p.Arg579Trp
ENST00000360144.7:c.1471C>T	ENSP00000353262.3:p.Arg491Trp
ENST00000369056.5:c.1738C>T	ENSP00000358052.1:p.Arg580Trp
ENST00000369058.7:c.1738C>T	ENSP00000358054.3:p.Arg580Trp
ENST00000369059.5:c.1393C>T	ENSP00000358055.1:p.Arg465Trp
ENST00000369060.8:c.1387C>T	ENSP00000358056.4:p.Arg463Trp
ENST00000369061.8:c.1399C>T	ENSP00000358057.4:p.Arg467Trp
ENST00000429361.5:c.511C>T	ENSP00000404219.1:p.Arg171Trp
ENST00000457416.6:c.1738C>T	ENSP00000410294.2:p.Arg580Trp
ENST00000478859.5:c.1051C>T	ENSP00000474011.1:p.Arg351Trp
ENST00000604236.5:c.*782C>T	ENSP00000474109.1:n.*782C>T
ENST00000613048.4:c.1468C>T	ENSP00000484154.1:p.Arg490Trp
NM_000141.4:c.1735C>T	NP_000132.3:p.Arg579Trp
NM_001144913.1:c.1738C>T	NP_001138385.1:p.Arg580Trp
NM_001144914.1:c.1399C>T	NP_001138386.1:p.Arg467Trp
NM_001144915.1:c.1468C>T	NP_001138387.1:p.Arg490Trp
NM_001144916.1:c.1390C>T	NP_001138388.1:p.Arg464Trp
NM_001144917.1:c.1387C>T	NP_001138389.1:p.Arg463Trp
NM_001144918.1:c.1384C>T	NP_001138390.1:p.Arg462Trp
NM_001144919.1:c.1471C>T	NP_001138391.1:p.Arg491Trp
NM_022970.3:c.1738C>T	NP_075259.4:p.Arg580Trp
NM_023029.2:c.1468C>T	NP_075418.1:p.Arg490Trp
NR_073009.1:n.2185C>T
XM_006717708.2:c.1789C>T	XP_006717771.1:p.Arg597Trp
XM_006717709.2:c.1786C>T	XP_006717772.1:p.Arg596Trp
XM_006717710.2:c.1795C>T	XP_006717773.1:p.Arg599Trp
XM_006717711.2:c.1528C>T	XP_006717774.1:p.Arg510Trp
XM_006717712.2:c.1450C>T	XP_006717775.1:p.Arg484Trp
XM_006717713.2:c.1792C>T	XP_006717776.1:p.Arg598Trp
XM_011539510.1:c.1051C>T	XP_011537812.1:p.Arg351Trp
NM_001320654.1:c.1051C>T	NP_001307583.1:p.Arg351Trp
NM_001320658.1:c.1729C>T	NP_001307587.1:p.Arg577Trp
XM_006717708.3:c.1789C>T	XP_006717771.1:p.Arg597Trp
XM_006717710.4:c.1795C>T	XP_006717773.1:p.Arg599Trp
XM_017015920.2:c.1789C>T	XP_016871409.1:p.Arg597Trp
XM_017015921.2:c.1786C>T	XP_016871410.1:p.Arg596Trp
XM_017015924.2:c.1447C>T	XP_016871413.1:p.Arg483Trp
XM_017015925.2:c.1441C>T	XP_016871414.1:p.Arg481Trp
XM_024447887.1:c.1525C>T	XP_024303655.1:p.Arg509Trp
XM_024447888.1:c.1522C>T	XP_024303656.1:p.Arg508Trp
XM_024447889.1:c.1519C>T	XP_024303657.1:p.Arg507Trp
XM_024447890.1:c.1528C>T	XP_024303658.1:p.Arg510Trp
XM_024447891.1:c.1450C>T	XP_024303659.1:p.Arg484Trp
XM_024447892.1:c.565C>T	XP_024303660.1:p.Arg189Trp
NM_000141.5:c.1735C>T MANE Select	NP_000132.3:p.Arg579Trp
NM_001144917.2:c.1387C>T	NP_001138389.1:p.Arg463Trp
NM_001144918.2:c.1384C>T	NP_001138390.1:p.Arg462Trp
NM_001144919.2:c.1471C>T	NP_001138391.1:p.Arg491Trp
NM_001320658.2:c.1729C>T	NP_001307587.1:p.Arg577Trp
NR_073009.2:n.2171C>T
NM_001144915.2:c.1468C>T	NP_001138387.1:p.Arg490Trp
NM_001144916.2:c.1390C>T	NP_001138388.1:p.Arg464Trp
NM_001320654.2:c.1051C>T	NP_001307583.1:p.Arg351Trp