Canonical Allele Identifier: CA2611199623

Gene: FGFR2

Linked Data

• gnomAD v4: 10-121517548-C-CGG

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121517552_121517553dup , CM000672.2:g.121517552_121517553dup	GRCh38
NC_000010.10:g.123277066_123277067dup , CM000672.1:g.123277066_123277067dup	GRCh37
NC_000010.9:g.123267056_123267057dup	NCBI36
NG_012449.1:g.85909_85910dup
NG_012449.2:g.85909_85910dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000457416.7:c.1087+1132_1087+1133dup MANE Plus Clinical	ENSP00000410294.2:n.1087+1132_1087+1133dup
ENST00000351936.11:c.940-87_940-86dup	ENSP00000309878.10:n.940-87_940-86dup
ENST00000638709.2:c.-231-87_-231-86dup	ENSP00000491912.2:n.-231-87_-231-86dup
ENST00000682296.1:n.288-87_288-86dup
ENST00000682400.1:n.595-87_595-86dup
ENST00000682550.1:c.595-87_595-86dup	ENSP00000507633.1:n.595-87_595-86dup
ENST00000682772.1:c.-231-87_-231-86dup	ENSP00000506848.1:n.-231-87_-231-86dup
ENST00000683211.1:c.940-87_940-86dup	ENSP00000508257.1:n.940-87_940-86dup
ENST00000683250.1:c.404-13609_404-13608dup	ENSP00000506847.1:n.404-13609_404-13608dup
ENST00000683418.1:n.3287-87_3287-86dup
ENST00000683678.1:n.940-87_940-86dup
ENST00000684153.1:c.595-87_595-86dup	ENSP00000506937.1:n.595-87_595-86dup
ENST00000358487.10:c.940-87_940-86dup MANE Select	ENSP00000351276.6:n.940-87_940-86dup
ENST00000336553.10:c.673-87_673-86dup	ENSP00000337665.6:n.673-87_673-86dup
ENST00000346997.6:c.940-87_940-86dup	ENSP00000263451.5:n.940-87_940-86dup
ENST00000351936.10:c.940-78_940-77dup	ENSP00000309878.9:n.940-78_940-77dup
ENST00000356226.8:c.595-87_595-86dup	ENSP00000348559.4:n.595-87_595-86dup
ENST00000357555.9:c.673-87_673-86dup	ENSP00000350166.5:n.673-87_673-86dup
ENST00000358487.9:c.940-87_940-86dup	ENSP00000351276.5:n.940-87_940-86dup
ENST00000360144.7:c.820+1132_820+1133dup	ENSP00000353262.3:n.820+1132_820+1133dup
ENST00000369056.5:c.1087+1132_1087+1133dup	ENSP00000358052.1:n.1087+1132_1087+1133dup
ENST00000369058.7:c.1087+1132_1087+1133dup	ENSP00000358054.3:n.1087+1132_1087+1133dup
ENST00000369059.5:c.742+1132_742+1133dup	ENSP00000358055.1:n.742+1132_742+1133dup
ENST00000369060.8:c.939+2429_939+2430dup	ENSP00000358056.4:n.939+2429_939+2430dup
ENST00000369061.8:c.749-2231_749-2230dup	ENSP00000358057.4:n.749-2231_749-2230dup
ENST00000457416.6:c.1087+1132_1087+1133dup	ENSP00000410294.2:n.1087+1132_1087+1133dup
ENST00000463870.5:n.149-87_149-86dup
ENST00000478859.5:c.256-87_256-86dup	ENSP00000474011.1:n.256-87_256-86dup
ENST00000490349.5:n.1349-87_1349-86dup
ENST00000604236.5:c.743-87_743-86dup	ENSP00000474109.1:n.743-87_743-86dup
ENST00000613048.4:c.673-87_673-86dup	ENSP00000484154.1:n.673-87_673-86dup
NM_000141.4:c.940-87_940-86dup	NP_000132.3:n.940-87_940-86dup
NM_001144913.1:c.1087+1132_1087+1133dup	NP_001138385.1:n.1087+1132_1087+1133dup
NM_001144914.1:c.749-2231_749-2230dup	NP_001138386.1:n.749-2231_749-2230dup
NM_001144915.1:c.673-87_673-86dup	NP_001138387.1:n.673-87_673-86dup
NM_001144916.1:c.595-87_595-86dup	NP_001138388.1:n.595-87_595-86dup
NM_001144917.1:c.939+2429_939+2430dup	NP_001138389.1:n.939+2429_939+2430dup
NM_001144918.1:c.595-87_595-86dup	NP_001138390.1:n.595-87_595-86dup
NM_001144919.1:c.820+1132_820+1133dup	NP_001138391.1:n.820+1132_820+1133dup
NM_022970.3:c.1087+1132_1087+1133dup	NP_075259.4:n.1087+1132_1087+1133dup
NM_023029.2:c.673-87_673-86dup	NP_075418.1:n.673-87_673-86dup
NR_073009.1:n.1390-87_1390-86dup
XM_006717708.2:c.1144+1132_1144+1133dup	XP_006717771.1:n.1144+1132_1144+1133dup
XM_006717709.2:c.997-87_997-86dup	XP_006717772.1:n.997-87_997-86dup
XM_006717710.2:c.1144+1132_1144+1133dup	XP_006717773.1:n.1144+1132_1144+1133dup
XM_006717711.2:c.877+1132_877+1133dup	XP_006717774.1:n.877+1132_877+1133dup
XM_006717712.2:c.799+1132_799+1133dup	XP_006717775.1:n.799+1132_799+1133dup
XM_006717713.2:c.997-87_997-86dup	XP_006717776.1:n.997-87_997-86dup
XM_011539510.1:c.256-87_256-86dup	XP_011537812.1:n.256-87_256-86dup
NM_001320654.1:c.256-87_256-86dup	NP_001307583.1:n.256-87_256-86dup
NM_001320658.1:c.940-87_940-86dup	NP_001307587.1:n.940-87_940-86dup
XM_006717708.3:c.1144+1132_1144+1133dup	XP_006717771.1:n.1144+1132_1144+1133dup
XM_006717710.4:c.1144+1132_1144+1133dup	XP_006717773.1:n.1144+1132_1144+1133dup
XM_017015920.2:c.1144+1132_1144+1133dup	XP_016871409.1:n.1144+1132_1144+1133dup
XM_017015921.2:c.997-87_997-86dup	XP_016871410.1:n.997-87_997-86dup
XM_017015924.2:c.652-87_652-86dup	XP_016871413.1:n.652-87_652-86dup
XM_017015925.2:c.652-87_652-86dup	XP_016871414.1:n.652-87_652-86dup
XM_024447887.1:c.730-87_730-86dup	XP_024303655.1:n.730-87_730-86dup
XM_024447888.1:c.877+1132_877+1133dup	XP_024303656.1:n.877+1132_877+1133dup
XM_024447889.1:c.730-87_730-86dup	XP_024303657.1:n.730-87_730-86dup
XM_024447890.1:c.877+1132_877+1133dup	XP_024303658.1:n.877+1132_877+1133dup
XM_024447891.1:c.799+1132_799+1133dup	XP_024303659.1:n.799+1132_799+1133dup
XM_024447892.1:c.-231-87_-231-86dup	XP_024303660.1:n.-231-87_-231-86dup
NM_000141.5:c.940-87_940-86dup MANE Select	NP_000132.3:n.940-87_940-86dup
NM_001144917.2:c.939+2429_939+2430dup	NP_001138389.1:n.939+2429_939+2430dup
NM_001144918.2:c.595-87_595-86dup	NP_001138390.1:n.595-87_595-86dup
NM_001144919.2:c.820+1132_820+1133dup	NP_001138391.1:n.820+1132_820+1133dup
NM_001320658.2:c.940-87_940-86dup	NP_001307587.1:n.940-87_940-86dup
NR_073009.2:n.1376-87_1376-86dup
NM_001144915.2:c.673-87_673-86dup	NP_001138387.1:n.673-87_673-86dup
NM_001144916.2:c.595-87_595-86dup	NP_001138388.1:n.595-87_595-86dup
NM_001320654.2:c.256-87_256-86dup	NP_001307583.1:n.256-87_256-86dup