Canonical Allele Identifier: CA10635077

Gene: FGFR2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121598109_121598110dup , CM000672.2:g.121598109_121598110dup	GRCh38
NC_000010.10:g.123357623_123357624dup , CM000672.1:g.123357623_123357624dup	GRCh37
NC_000010.9:g.123347613_123347614dup	NCBI36
NG_012449.1:g.5350_5351dup
NG_012449.2:g.5350_5351dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000457416.7:c.-298_-297dup MANE Plus Clinical	ENSP00000410294.2:n.-298_-297dup
ENST00000684153.1:c.-298_-297dup	ENSP00000506937.1:n.-298_-297dup
ENST00000358487.10:c.-298_-297dup MANE Select	ENSP00000351276.6:n.-298_-297dup
ENST00000336553.10:c.-298_-297dup	ENSP00000337665.6:n.-298_-297dup
ENST00000356226.8:c.-298_-297dup	ENSP00000348559.4:n.-298_-297dup
ENST00000359354.6:c.-298_-297dup	ENSP00000352309.2:n.-298_-297dup
ENST00000360144.7:c.-298_-297dup	ENSP00000353262.3:n.-298_-297dup
ENST00000369058.7:c.-298_-297dup	ENSP00000358054.3:n.-298_-297dup
ENST00000369059.5:c.-298_-297dup	ENSP00000358055.1:n.-298_-297dup
ENST00000369060.8:c.-298_-297dup	ENSP00000358056.4:n.-298_-297dup
ENST00000457416.6:c.-298_-297dup	ENSP00000410294.2:n.-298_-297dup
ENST00000604236.5:c.-298_-297dup	ENSP00000474109.1:n.-298_-297dup
ENST00000613048.4:c.-298_-297dup	ENSP00000484154.1:n.-298_-297dup
NM_000141.4:c.-298_-297dup	NP_000132.3:n.-298_-297dup
NM_001144917.1:c.-298_-297dup	NP_001138389.1:n.-298_-297dup
NM_001144918.1:c.-298_-297dup	NP_001138390.1:n.-298_-297dup
NM_001144919.1:c.-298_-297dup	NP_001138391.1:n.-298_-297dup
NM_022970.3:c.-298_-297dup	NP_075259.4:n.-298_-297dup
NR_073009.1:n.350_351dup
XM_006717708.2:c.-241_-240dup	XP_006717771.1:n.-241_-240dup
XM_006717709.2:c.-241_-240dup	XP_006717772.1:n.-241_-240dup
XM_006717710.2:c.-241_-240dup	XP_006717773.1:n.-241_-240dup
XM_006717713.2:c.-241_-240dup	XP_006717776.1:n.-241_-240dup
NM_001320658.1:c.-298_-297dup	NP_001307587.1:n.-298_-297dup
XM_017015925.2:c.-241_-240dup	XP_016871414.1:n.-241_-240dup
XM_024447890.1:c.-241_-240dup	XP_024303658.1:n.-241_-240dup
NM_000141.5:c.-298_-297dup MANE Select	NP_000132.3:n.-298_-297dup
NM_001144917.2:c.-298_-297dup	NP_001138389.1:n.-298_-297dup
NM_001144918.2:c.-298_-297dup	NP_001138390.1:n.-298_-297dup
NM_001144919.2:c.-298_-297dup	NP_001138391.1:n.-298_-297dup
NM_001320658.2:c.-298_-297dup	NP_001307587.1:n.-298_-297dup
NR_073009.2:n.336_337dup