Canonical Allele Identifier: CA378327009
Gene: FGFR2 HGNC NCBI

Linked Data

dbSNP Id: rs1355130739

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121515154T>A , CM000672.2:g.121515154T>A GRCh38
NC_000010.10:g.123274668T>A , CM000672.1:g.123274668T>A GRCh37
NC_000010.9:g.123264658T>A NCBI36
NG_012449.1:g.88305A>T
NG_012449.2:g.88305A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000457416.7:c.1253A>T MANE Plus Clinical ENSP00000410294.2:p.Lys418Met
ENST00000351936.11:c.1250A>T ENSP00000309878.10:p.Lys417Met
ENST00000638709.2:c.80A>T ENSP00000491912.2:p.Lys27Met
ENST00000682296.1:n.598A>T
ENST00000682550.1:c.905A>T ENSP00000507633.1:p.Lys302Met
ENST00000682772.1:c.80A>T ENSP00000506848.1:p.Lys27Met
ENST00000683211.1:c.1250A>T ENSP00000508257.1:p.Lys417Met
ENST00000683250.1:c.404-11213A>T ENSP00000506847.1:n.404-11213A>T
ENST00000683418.1:n.3597A>T
ENST00000684153.1:c.905A>T ENSP00000506937.1:p.Lys302Met
ENST00000358487.10:c.1250A>T MANE Select ENSP00000351276.6:p.Lys417Met
ENST00000336553.10:c.983A>T ENSP00000337665.6:p.Lys328Met
ENST00000346997.6:c.1250A>T ENSP00000263451.5:p.Lys417Met
ENST00000351936.10:c.1256A>T ENSP00000309878.9:p.Lys419Met
ENST00000356226.8:c.905A>T ENSP00000348559.4:p.Lys302Met
ENST00000357555.9:c.983A>T ENSP00000350166.5:p.Lys328Met
ENST00000358487.9:c.1250A>T ENSP00000351276.5:p.Lys417Met
ENST00000360144.7:c.986A>T ENSP00000353262.3:p.Lys329Met
ENST00000369056.5:c.1253A>T ENSP00000358052.1:p.Lys418Met
ENST00000369058.7:c.1253A>T ENSP00000358054.3:p.Lys418Met
ENST00000369059.5:c.908A>T ENSP00000358055.1:p.Lys303Met
ENST00000369060.8:c.939+4825A>T ENSP00000358056.4:n.939+4825A>T
ENST00000369061.8:c.914A>T ENSP00000358057.4:p.Lys305Met
ENST00000429361.5:c.26A>T ENSP00000404219.1:p.Lys9Met
ENST00000457416.6:c.1253A>T ENSP00000410294.2:p.Lys418Met
ENST00000478859.5:c.566A>T ENSP00000474011.1:p.Lys189Met
ENST00000604236.5:c.*297A>T ENSP00000474109.1:n.*297A>T
ENST00000613048.4:c.983A>T ENSP00000484154.1:p.Lys328Met
NM_000141.4:c.1250A>T NP_000132.3:p.Lys417Met
NM_001144913.1:c.1253A>T NP_001138385.1:p.Lys418Met
NM_001144914.1:c.914A>T NP_001138386.1:p.Lys305Met
NM_001144915.1:c.983A>T NP_001138387.1:p.Lys328Met
NM_001144916.1:c.905A>T NP_001138388.1:p.Lys302Met
NM_001144917.1:c.939+4825A>T NP_001138389.1:n.939+4825A>T
NM_001144918.1:c.905A>T NP_001138390.1:p.Lys302Met
NM_001144919.1:c.986A>T NP_001138391.1:p.Lys329Met
NM_022970.3:c.1253A>T NP_075259.4:p.Lys418Met
NM_023029.2:c.983A>T NP_075418.1:p.Lys328Met
NR_073009.1:n.1700A>T
XM_006717708.2:c.1310A>T XP_006717771.1:p.Lys437Met
XM_006717709.2:c.1307A>T XP_006717772.1:p.Lys436Met
XM_006717710.2:c.1310A>T XP_006717773.1:p.Lys437Met
XM_006717711.2:c.1043A>T XP_006717774.1:p.Lys348Met
XM_006717712.2:c.965A>T XP_006717775.1:p.Lys322Met
XM_006717713.2:c.1307A>T XP_006717776.1:p.Lys436Met
XM_011539510.1:c.566A>T XP_011537812.1:p.Lys189Met
NM_001320654.1:c.566A>T NP_001307583.1:p.Lys189Met
NM_001320658.1:c.1250A>T NP_001307587.1:p.Lys417Met
XM_006717708.3:c.1310A>T XP_006717771.1:p.Lys437Met
XM_006717710.4:c.1310A>T XP_006717773.1:p.Lys437Met
XM_017015920.2:c.1310A>T XP_016871409.1:p.Lys437Met
XM_017015921.2:c.1307A>T XP_016871410.1:p.Lys436Met
XM_017015924.2:c.962A>T XP_016871413.1:p.Lys321Met
XM_017015925.2:c.962A>T XP_016871414.1:p.Lys321Met
XM_024447887.1:c.1040A>T XP_024303655.1:p.Lys347Met
XM_024447888.1:c.1043A>T XP_024303656.1:p.Lys348Met
XM_024447889.1:c.1040A>T XP_024303657.1:p.Lys347Met
XM_024447890.1:c.1043A>T XP_024303658.1:p.Lys348Met
XM_024447891.1:c.965A>T XP_024303659.1:p.Lys322Met
XM_024447892.1:c.80A>T XP_024303660.1:p.Lys27Met
NM_000141.5:c.1250A>T MANE Select NP_000132.3:p.Lys417Met
NM_001144917.2:c.939+4825A>T NP_001138389.1:n.939+4825A>T
NM_001144918.2:c.905A>T NP_001138390.1:p.Lys302Met
NM_001144919.2:c.986A>T NP_001138391.1:p.Lys329Met
NM_001320658.2:c.1250A>T NP_001307587.1:p.Lys417Met
NR_073009.2:n.1686A>T
NM_001144915.2:c.983A>T NP_001138387.1:p.Lys328Met
NM_001144916.2:c.905A>T NP_001138388.1:p.Lys302Met
NM_001320654.2:c.566A>T NP_001307583.1:p.Lys189Met