Canonical Allele Identifier: CA16602610
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 376153
ClinVar RCV Id: RCV000417597
dbSNP Id: rs1057519795

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121488002T>C , CM000672.2:g.121488002T>C GRCh38
NC_000010.10:g.123247516T>C , CM000672.1:g.123247516T>C GRCh37
NC_000010.9:g.123237506T>C NCBI36
NG_012449.1:g.115457A>G
NG_012449.2:g.115457A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000457416.7:c.1978A>G MANE Plus Clinical ENSP00000410294.2:p.Lys660Glu
ENST00000351936.11:c.1969A>G ENSP00000309878.10:p.Lys657Glu
ENST00000638709.2:c.799A>G ENSP00000491912.2:p.Lys267Glu
ENST00000682296.1:n.1317A>G
ENST00000682550.1:c.1624A>G ENSP00000507633.1:p.Lys542Glu
ENST00000682772.1:c.799A>G ENSP00000506848.1:p.Lys267Glu
ENST00000682904.1:n.795A>G
ENST00000683029.1:n.387A>G
ENST00000683211.1:c.1969A>G ENSP00000508257.1:p.Lys657Glu
ENST00000683250.1:c.*677A>G ENSP00000506847.1:n.*677A>G
ENST00000683418.1:n.4316A>G
ENST00000684153.1:c.1624A>G ENSP00000506937.1:p.Lys542Glu
ENST00000684516.1:n.2988A>G
ENST00000358487.10:c.1975A>G MANE Select ENSP00000351276.6:p.Lys659Glu
ENST00000336553.10:c.1702A>G ENSP00000337665.6:p.Lys568Glu
ENST00000346997.6:c.1969A>G ENSP00000263451.5:p.Lys657Glu
ENST00000351936.10:c.1975A>G ENSP00000309878.9:p.Lys659Glu
ENST00000356226.8:c.1624A>G ENSP00000348559.4:p.Lys542Glu
ENST00000357555.9:c.1708A>G ENSP00000350166.5:p.Lys570Glu
ENST00000358487.9:c.1975A>G ENSP00000351276.5:p.Lys659Glu
ENST00000360144.7:c.1711A>G ENSP00000353262.3:p.Lys571Glu
ENST00000369056.5:c.1978A>G ENSP00000358052.1:p.Lys660Glu
ENST00000369058.7:c.1978A>G ENSP00000358054.3:p.Lys660Glu
ENST00000369059.5:c.1633A>G ENSP00000358055.1:p.Lys545Glu
ENST00000369060.8:c.1627A>G ENSP00000358056.4:p.Lys543Glu
ENST00000369061.8:c.1639A>G ENSP00000358057.4:p.Lys547Glu
ENST00000429361.5:c.751A>G ENSP00000404219.1:p.Lys251Glu
ENST00000457416.6:c.1978A>G ENSP00000410294.2:p.Lys660Glu
ENST00000478859.5:c.1291A>G ENSP00000474011.1:p.Lys431Glu
ENST00000604236.5:c.*1022A>G ENSP00000474109.1:n.*1022A>G
ENST00000613048.4:c.1708A>G ENSP00000484154.1:p.Lys570Glu
NM_000141.4:c.1975A>G NP_000132.3:p.Lys659Glu
NM_001144913.1:c.1978A>G NP_001138385.1:p.Lys660Glu
NM_001144914.1:c.1639A>G NP_001138386.1:p.Lys547Glu
NM_001144915.1:c.1708A>G NP_001138387.1:p.Lys570Glu
NM_001144916.1:c.1630A>G NP_001138388.1:p.Lys544Glu
NM_001144917.1:c.1627A>G NP_001138389.1:p.Lys543Glu
NM_001144918.1:c.1624A>G NP_001138390.1:p.Lys542Glu
NM_001144919.1:c.1711A>G NP_001138391.1:p.Lys571Glu
NM_022970.3:c.1978A>G NP_075259.4:p.Lys660Glu
NM_023029.2:c.1708A>G NP_075418.1:p.Lys570Glu
NR_073009.1:n.2425A>G
XM_006717708.2:c.2029A>G XP_006717771.1:p.Lys677Glu
XM_006717709.2:c.2026A>G XP_006717772.1:p.Lys676Glu
XM_006717710.2:c.2035A>G XP_006717773.1:p.Lys679Glu
XM_006717711.2:c.1768A>G XP_006717774.1:p.Lys590Glu
XM_006717712.2:c.1690A>G XP_006717775.1:p.Lys564Glu
XM_006717713.2:c.2032A>G XP_006717776.1:p.Lys678Glu
XM_011539510.1:c.1291A>G XP_011537812.1:p.Lys431Glu
NM_001320654.1:c.1291A>G NP_001307583.1:p.Lys431Glu
NM_001320658.1:c.1969A>G NP_001307587.1:p.Lys657Glu
XM_006717708.3:c.2029A>G XP_006717771.1:p.Lys677Glu
XM_006717710.4:c.2035A>G XP_006717773.1:p.Lys679Glu
XM_017015920.2:c.2029A>G XP_016871409.1:p.Lys677Glu
XM_017015921.2:c.2026A>G XP_016871410.1:p.Lys676Glu
XM_017015924.2:c.1687A>G XP_016871413.1:p.Lys563Glu
XM_017015925.2:c.1681A>G XP_016871414.1:p.Lys561Glu
XM_024447887.1:c.1765A>G XP_024303655.1:p.Lys589Glu
XM_024447888.1:c.1762A>G XP_024303656.1:p.Lys588Glu
XM_024447889.1:c.1759A>G XP_024303657.1:p.Lys587Glu
XM_024447890.1:c.1768A>G XP_024303658.1:p.Lys590Glu
XM_024447891.1:c.1690A>G XP_024303659.1:p.Lys564Glu
XM_024447892.1:c.805A>G XP_024303660.1:p.Lys269Glu
NM_000141.5:c.1975A>G MANE Select NP_000132.3:p.Lys659Glu
NM_001144917.2:c.1627A>G NP_001138389.1:p.Lys543Glu
NM_001144918.2:c.1624A>G NP_001138390.1:p.Lys542Glu
NM_001144919.2:c.1711A>G NP_001138391.1:p.Lys571Glu
NM_001320658.2:c.1969A>G NP_001307587.1:p.Lys657Glu
NR_073009.2:n.2411A>G
NM_001144915.2:c.1708A>G NP_001138387.1:p.Lys570Glu
NM_001144916.2:c.1630A>G NP_001138388.1:p.Lys544Glu
NM_001320654.2:c.1291A>G NP_001307583.1:p.Lys431Glu