Canonical Allele Identifier: CA378328101
Gene: FGFR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121517393G>C , CM000672.2:g.121517393G>C GRCh38
NC_000010.10:g.123276907G>C , CM000672.1:g.123276907G>C GRCh37
NC_000010.9:g.123266897G>C NCBI36
NG_012449.1:g.86066C>G
NG_012449.2:g.86066C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000358487.10:c.1010C>G MANE Select ENSP00000351276.6:p.Ala337Gly
ENST00000336553.10:c.743C>G ENSP00000337665.6:p.Ala248Gly
ENST00000346997.6:c.1010C>G ENSP00000263451.5:p.Ala337Gly
ENST00000351936.10:c.1016C>G ENSP00000309878.9:p.Ala339Gly
ENST00000356226.8:c.665C>G ENSP00000348559.4:p.Ala222Gly
ENST00000357555.9:c.743C>G ENSP00000350166.5:p.Ala248Gly
ENST00000358487.9:c.1010C>G ENSP00000351276.5:p.Ala337Gly
ENST00000360144.7:c.820+1289C>G ENSP00000353262.3:p.=
ENST00000369056.5:c.1087+1289C>G ENSP00000358052.1:p.=
ENST00000369058.7:c.1087+1289C>G ENSP00000358054.3:p.=
ENST00000369059.5:c.742+1289C>G ENSP00000358055.1:p.=
ENST00000369060.8:c.939+2586C>G ENSP00000358056.4:p.=
ENST00000369061.8:c.749-2074C>G ENSP00000358057.4:p.=
ENST00000457416.6:c.1087+1289C>G ENSP00000410294.2:p.=
ENST00000463870.5:n.219C>G
ENST00000478859.5:c.326C>G ENSP00000474011.1:p.Ala109Gly
ENST00000490349.5:n.1419C>G
ENST00000604236.5:c.*57C>G ENSP00000474109.1:p.=
ENST00000613048.4:c.743C>G ENSP00000484154.1:p.Ala248Gly
NM_000141.4:c.1010C>G NP_000132.3:p.Ala337Gly
NM_001144913.1:c.1087+1289C>G NP_001138385.1:p.=
NM_001144914.1:c.749-2074C>G NP_001138386.1:p.=
NM_001144915.1:c.743C>G NP_001138387.1:p.Ala248Gly
NM_001144916.1:c.665C>G NP_001138388.1:p.Ala222Gly
NM_001144917.1:c.939+2586C>G NP_001138389.1:p.=
NM_001144918.1:c.665C>G NP_001138390.1:p.Ala222Gly
NM_001144919.1:c.820+1289C>G NP_001138391.1:p.=
NM_022970.3:c.1087+1289C>G NP_075259.4:p.=
NM_023029.2:c.743C>G NP_075418.1:p.Ala248Gly
NR_073009.1:n.1460C>G
XM_006717708.2:c.1144+1289C>G XP_006717771.1:p.=
XM_006717709.2:c.1067C>G XP_006717772.1:p.Ala356Gly
XM_006717710.2:c.1144+1289C>G XP_006717773.1:p.=
XM_006717711.2:c.877+1289C>G XP_006717774.1:p.=
XM_006717712.2:c.799+1289C>G XP_006717775.1:p.=
XM_006717713.2:c.1067C>G XP_006717776.1:p.Ala356Gly
XM_011539510.1:c.326C>G XP_011537812.1:p.Ala109Gly
NM_001320654.1:c.326C>G NP_001307583.1:p.Ala109Gly
NM_001320658.1:c.1010C>G NP_001307587.1:p.Ala337Gly
XM_006717708.3:c.1144+1289C>G XP_006717771.1:p.=
XM_006717710.4:c.1144+1289C>G XP_006717773.1:p.=
XM_017015920.2:c.1144+1289C>G XP_016871409.1:p.=
XM_017015921.2:c.1067C>G XP_016871410.1:p.Ala356Gly
XM_017015924.2:c.722C>G XP_016871413.1:p.Ala241Gly
XM_017015925.2:c.722C>G XP_016871414.1:p.Ala241Gly
XM_024447887.1:c.800C>G XP_024303655.1:p.Ala267Gly
XM_024447888.1:c.877+1289C>G XP_024303656.1:p.=
XM_024447889.1:c.800C>G XP_024303657.1:p.Ala267Gly
XM_024447890.1:c.877+1289C>G XP_024303658.1:p.=
XM_024447891.1:c.799+1289C>G XP_024303659.1:p.=
XM_024447892.1:c.-161C>G XP_024303660.1:p.=
NM_000141.5:c.1010C>G MANE Select NP_000132.3:p.Ala337Gly
NM_001144917.2:c.939+2586C>G NP_001138389.1:p.=
NM_001144918.2:c.665C>G NP_001138390.1:p.Ala222Gly
NM_001144919.2:c.820+1289C>G NP_001138391.1:p.=
NM_001320658.2:c.1010C>G NP_001307587.1:p.Ala337Gly
NR_073009.2:n.1446C>G
NM_001144915.2:c.743C>G NP_001138387.1:p.Ala248Gly
NM_001144916.2:c.665C>G NP_001138388.1:p.Ala222Gly
NM_001320654.2:c.326C>G NP_001307583.1:p.Ala109Gly