Canonical Allele Identifier: CA1941060818
Gene: FGFR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121594354_121594355delinsTC , CM000672.2:g.121594354_121594355delinsTC GRCh38
NC_000010.10:g.123353868_123353869delinsTC , CM000672.1:g.123353868_123353869delinsTC GRCh37
NC_000010.9:g.123343858_123343859delinsTC NCBI36
NG_012449.1:g.9104_9105delinsGA
NG_012449.2:g.9104_9105delinsGA

Transcript Alleles

HGVS Amino-acid change
ENST00000457416.7:c.-150-388_-150-387delinsGA MANE Plus Clinical ENSP00000410294.2:n.-150-388_-150-387deli...
ENST00000351936.11:c.-151+200_-151+201delinsGA ENSP00000309878.10:n.-151+200_-151+201del...
ENST00000682550.1:c.-150-388_-150-387delinsGA ENSP00000507633.1:n.-150-388_-150-387deli...
ENST00000683035.1:c.-538_-537delinsGA ENSP00000507074.1:n.-538_-537delinsGA
ENST00000683211.1:c.-538_-537delinsGA ENSP00000508257.1:n.-538_-537delinsGA
ENST00000683250.1:c.-394_-393delinsGA ENSP00000506847.1:n.-394_-393delinsGA
ENST00000684153.1:c.-150-388_-150-387delinsGA ENSP00000506937.1:n.-150-388_-150-387deli...
ENST00000358487.10:c.-150-388_-150-387delinsGA MANE Select ENSP00000351276.6:n.-150-388_-150-387deli...
ENST00000636922.1:c.-150-388_-150-387delinsGA ENSP00000490905.1:n.-150-388_-150-387deli...
ENST00000336553.10:c.-150-388_-150-387delinsGA ENSP00000337665.6:n.-150-388_-150-387deli...
ENST00000356226.8:c.-150-388_-150-387delinsGA ENSP00000348559.4:n.-150-388_-150-387deli...
ENST00000357555.9:c.-150-388_-150-387delinsGA ENSP00000350166.5:n.-150-388_-150-387deli...
ENST00000358487.9:c.-150-388_-150-387delinsGA ENSP00000351276.5:n.-150-388_-150-387deli...
ENST00000359354.6:c.-150-388_-150-387delinsGA ENSP00000352309.2:n.-150-388_-150-387deli...
ENST00000360144.7:c.-150-388_-150-387delinsGA ENSP00000353262.3:n.-150-388_-150-387deli...
ENST00000369058.7:c.-150-388_-150-387delinsGA ENSP00000358054.3:n.-150-388_-150-387deli...
ENST00000369059.5:c.-150-388_-150-387delinsGA ENSP00000358055.1:n.-150-388_-150-387deli...
ENST00000369060.8:c.-150-388_-150-387delinsGA ENSP00000358056.4:n.-150-388_-150-387deli...
ENST00000457416.6:c.-150-388_-150-387delinsGA ENSP00000410294.2:n.-150-388_-150-387deli...
ENST00000490349.5:n.112-388_112-387delinsGA
ENST00000604236.5:c.-150-388_-150-387delinsGA ENSP00000474109.1:n.-150-388_-150-387deli...
ENST00000613048.4:c.-150-388_-150-387delinsGA ENSP00000484154.1:n.-150-388_-150-387deli...
NM_000141.4:c.-150-388_-150-387delinsGA NP_000132.3:n.-150-388_-150-387delinsGA
NM_001144915.1:c.-150-388_-150-387delinsGA NP_001138387.1:n.-150-388_-150-387delinsG...
NM_001144917.1:c.-150-388_-150-387delinsGA NP_001138389.1:n.-150-388_-150-387delinsG...
NM_001144918.1:c.-150-388_-150-387delinsGA NP_001138390.1:n.-150-388_-150-387delinsG...
NM_001144919.1:c.-150-388_-150-387delinsGA NP_001138391.1:n.-150-388_-150-387delinsG...
NM_022970.3:c.-150-388_-150-387delinsGA NP_075259.4:n.-150-388_-150-387delinsGA
NR_073009.1:n.498-388_498-387delinsGA
XM_006717708.2:c.-93-388_-93-387delinsGA XP_006717771.1:n.-93-388_-93-387delinsGA
XM_006717709.2:c.-93-388_-93-387delinsGA XP_006717772.1:n.-93-388_-93-387delinsGA
XM_006717710.2:c.-93-388_-93-387delinsGA XP_006717773.1:n.-93-388_-93-387delinsGA
XM_006717713.2:c.-93-388_-93-387delinsGA XP_006717776.1:n.-93-388_-93-387delinsGA
NM_001320658.1:c.-150-388_-150-387delinsGA NP_001307587.1:n.-150-388_-150-387delinsG...
XM_006717708.3:c.-93-388_-93-387delinsGA XP_006717771.1:n.-93-388_-93-387delinsGA
XM_006717710.4:c.-93-388_-93-387delinsGA XP_006717773.1:n.-93-388_-93-387delinsGA
XM_017015920.2:c.-93-388_-93-387delinsGA XP_016871409.1:n.-93-388_-93-387delinsGA
XM_017015921.2:c.-93-388_-93-387delinsGA XP_016871410.1:n.-93-388_-93-387delinsGA
XM_017015924.2:c.-93-388_-93-387delinsGA XP_016871413.1:n.-93-388_-93-387delinsGA
XM_017015925.2:c.-93-388_-93-387delinsGA XP_016871414.1:n.-93-388_-93-387delinsGA
XM_024447887.1:c.-93-388_-93-387delinsGA XP_024303655.1:n.-93-388_-93-387delinsGA
XM_024447888.1:c.-93-388_-93-387delinsGA XP_024303656.1:n.-93-388_-93-387delinsGA
XM_024447889.1:c.-93-388_-93-387delinsGA XP_024303657.1:n.-93-388_-93-387delinsGA
XM_024447890.1:c.-93-388_-93-387delinsGA XP_024303658.1:n.-93-388_-93-387delinsGA
XM_024447891.1:c.-93-388_-93-387delinsGA XP_024303659.1:n.-93-388_-93-387delinsGA
NM_000141.5:c.-150-388_-150-387delinsGA MANE Select NP_000132.3:n.-150-388_-150-387delinsGA
NM_001144917.2:c.-150-388_-150-387delinsGA NP_001138389.1:n.-150-388_-150-387delinsG...
NM_001144918.2:c.-150-388_-150-387delinsGA NP_001138390.1:n.-150-388_-150-387delinsG...
NM_001144919.2:c.-150-388_-150-387delinsGA NP_001138391.1:n.-150-388_-150-387delinsG...
NM_001320658.2:c.-150-388_-150-387delinsGA NP_001307587.1:n.-150-388_-150-387delinsG...
NR_073009.2:n.484-388_484-387delinsGA
NM_001144915.2:c.-150-388_-150-387delinsGA NP_001138387.1:n.-150-388_-150-387delinsG...