Canonical Allele Identifier: CA1941060672

Gene: FGFR2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121594065_121594069delinsGCAAA , CM000672.2:g.121594065_121594069delinsGCAAA	GRCh38
NC_000010.10:g.123353579_123353583delinsGCAAA , CM000672.1:g.123353579_123353583delinsGCAAA	GRCh37
NC_000010.9:g.123343569_123343573delinsGCAAA	NCBI36
NG_012449.1:g.9390_9394delinsTTTGC
NG_012449.2:g.9390_9394delinsTTTGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000457416.7:c.-150-102_-150-98delinsTTTGC MANE Plus Clinical	ENSP00000410294.2:n.-150-102_-150-98delinsTTTGC
ENST00000351936.11:c.-150-102_-150-98delinsTTTGC	ENSP00000309878.10:n.-150-102_-150-98delinsTTTGC
ENST00000682550.1:c.-150-102_-150-98delinsTTTGC	ENSP00000507633.1:n.-150-102_-150-98delinsTTTGC
ENST00000683035.1:c.-252_-248delinsTTTGC	ENSP00000507074.1:n.-252_-248delinsTTTGC
ENST00000683211.1:c.-252_-248delinsTTTGC	ENSP00000508257.1:n.-252_-248delinsTTTGC
ENST00000683250.1:c.-151+43_-151+47delinsTTTGC	ENSP00000506847.1:n.-151+43_-151+47delinsTTTGC
ENST00000684153.1:c.-150-102_-150-98delinsTTTGC	ENSP00000506937.1:n.-150-102_-150-98delinsTTTGC
ENST00000358487.10:c.-150-102_-150-98delinsTTTGC MANE Select	ENSP00000351276.6:n.-150-102_-150-98delinsTTTGC
ENST00000636922.1:c.-150-102_-150-98delinsTTTGC	ENSP00000490905.1:n.-150-102_-150-98delinsTTTGC
ENST00000336553.10:c.-150-102_-150-98delinsTTTGC	ENSP00000337665.6:n.-150-102_-150-98delinsTTTGC
ENST00000356226.8:c.-150-102_-150-98delinsTTTGC	ENSP00000348559.4:n.-150-102_-150-98delinsTTTGC
ENST00000357555.9:c.-150-102_-150-98delinsTTTGC	ENSP00000350166.5:n.-150-102_-150-98delinsTTTGC
ENST00000358487.9:c.-150-102_-150-98delinsTTTGC	ENSP00000351276.5:n.-150-102_-150-98delinsTTTGC
ENST00000359354.6:c.-150-102_-150-98delinsTTTGC	ENSP00000352309.2:n.-150-102_-150-98delinsTTTGC
ENST00000360144.7:c.-150-102_-150-98delinsTTTGC	ENSP00000353262.3:n.-150-102_-150-98delinsTTTGC
ENST00000369058.7:c.-150-102_-150-98delinsTTTGC	ENSP00000358054.3:n.-150-102_-150-98delinsTTTGC
ENST00000369059.5:c.-150-102_-150-98delinsTTTGC	ENSP00000358055.1:n.-150-102_-150-98delinsTTTGC
ENST00000369060.8:c.-150-102_-150-98delinsTTTGC	ENSP00000358056.4:n.-150-102_-150-98delinsTTTGC
ENST00000457416.6:c.-150-102_-150-98delinsTTTGC	ENSP00000410294.2:n.-150-102_-150-98delinsTTTGC
ENST00000490349.5:n.112-102_112-98delinsTTTGC
ENST00000491111.1:n.42+43_42+47delinsTTTGC
ENST00000604236.5:c.-150-102_-150-98delinsTTTGC	ENSP00000474109.1:n.-150-102_-150-98delinsTTTGC
ENST00000613048.4:c.-150-102_-150-98delinsTTTGC	ENSP00000484154.1:n.-150-102_-150-98delinsTTTGC
NM_000141.4:c.-150-102_-150-98delinsTTTGC	NP_000132.3:n.-150-102_-150-98delinsTTTGC
NM_001144915.1:c.-150-102_-150-98delinsTTTGC	NP_001138387.1:n.-150-102_-150-98delinsTTTGC
NM_001144916.1:c.-252_-248delinsTTTGC	NP_001138388.1:n.-252_-248delinsTTTGC
NM_001144917.1:c.-150-102_-150-98delinsTTTGC	NP_001138389.1:n.-150-102_-150-98delinsTTTGC
NM_001144918.1:c.-150-102_-150-98delinsTTTGC	NP_001138390.1:n.-150-102_-150-98delinsTTTGC
NM_001144919.1:c.-150-102_-150-98delinsTTTGC	NP_001138391.1:n.-150-102_-150-98delinsTTTGC
NM_022970.3:c.-150-102_-150-98delinsTTTGC	NP_075259.4:n.-150-102_-150-98delinsTTTGC
NR_073009.1:n.498-102_498-98delinsTTTGC
XM_006717708.2:c.-93-102_-93-98delinsTTTGC	XP_006717771.1:n.-93-102_-93-98delinsTTTGC
XM_006717709.2:c.-93-102_-93-98delinsTTTGC	XP_006717772.1:n.-93-102_-93-98delinsTTTGC
XM_006717710.2:c.-93-102_-93-98delinsTTTGC	XP_006717773.1:n.-93-102_-93-98delinsTTTGC
XM_006717713.2:c.-93-102_-93-98delinsTTTGC	XP_006717776.1:n.-93-102_-93-98delinsTTTGC
NM_001320658.1:c.-150-102_-150-98delinsTTTGC	NP_001307587.1:n.-150-102_-150-98delinsTTTGC
XM_006717708.3:c.-93-102_-93-98delinsTTTGC	XP_006717771.1:n.-93-102_-93-98delinsTTTGC
XM_006717710.4:c.-93-102_-93-98delinsTTTGC	XP_006717773.1:n.-93-102_-93-98delinsTTTGC
XM_017015920.2:c.-93-102_-93-98delinsTTTGC	XP_016871409.1:n.-93-102_-93-98delinsTTTGC
XM_017015921.2:c.-93-102_-93-98delinsTTTGC	XP_016871410.1:n.-93-102_-93-98delinsTTTGC
XM_017015924.2:c.-93-102_-93-98delinsTTTGC	XP_016871413.1:n.-93-102_-93-98delinsTTTGC
XM_017015925.2:c.-93-102_-93-98delinsTTTGC	XP_016871414.1:n.-93-102_-93-98delinsTTTGC
XM_024447887.1:c.-93-102_-93-98delinsTTTGC	XP_024303655.1:n.-93-102_-93-98delinsTTTGC
XM_024447888.1:c.-93-102_-93-98delinsTTTGC	XP_024303656.1:n.-93-102_-93-98delinsTTTGC
XM_024447889.1:c.-93-102_-93-98delinsTTTGC	XP_024303657.1:n.-93-102_-93-98delinsTTTGC
XM_024447890.1:c.-93-102_-93-98delinsTTTGC	XP_024303658.1:n.-93-102_-93-98delinsTTTGC
XM_024447891.1:c.-93-102_-93-98delinsTTTGC	XP_024303659.1:n.-93-102_-93-98delinsTTTGC
NM_000141.5:c.-150-102_-150-98delinsTTTGC MANE Select	NP_000132.3:n.-150-102_-150-98delinsTTTGC
NM_001144917.2:c.-150-102_-150-98delinsTTTGC	NP_001138389.1:n.-150-102_-150-98delinsTTTGC
NM_001144918.2:c.-150-102_-150-98delinsTTTGC	NP_001138390.1:n.-150-102_-150-98delinsTTTGC
NM_001144919.2:c.-150-102_-150-98delinsTTTGC	NP_001138391.1:n.-150-102_-150-98delinsTTTGC
NM_001320658.2:c.-150-102_-150-98delinsTTTGC	NP_001307587.1:n.-150-102_-150-98delinsTTTGC
NR_073009.2:n.484-102_484-98delinsTTTGC
NM_001144915.2:c.-150-102_-150-98delinsTTTGC	NP_001138387.1:n.-150-102_-150-98delinsTTTGC
NM_001144916.2:c.-252_-248delinsTTTGC	NP_001138388.1:n.-252_-248delinsTTTGC