Canonical Allele Identifier: CA891862926

Gene: FGFR2

Linked Data

• ClinVar Variation Id: 29852
• ClinVar RCV Id: RCV000022731
• dbSNP Id: rs1554930637

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121520001_121520063del , CM000672.2:g.121520001_121520063del	GRCh38
NC_000010.10:g.123279515_123279577del , CM000672.1:g.123279515_123279577del	GRCh37
NC_000010.9:g.123269505_123269567del	NCBI36
NG_012449.1:g.83400_83462del
NG_012449.2:g.83400_83462del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000457416.7:c.859_921del MANE Plus Clinical	ENSP00000410294.2:p.His287_Pro307del
ENST00000351936.11:c.859_921del	ENSP00000309878.10:p.His287_Pro307del
ENST00000638709.2:c.-312_-250del	ENSP00000491912.2:n.-312_-250del
ENST00000682296.1:n.207_269del
ENST00000682400.1:n.514_576del
ENST00000682550.1:c.514_576del	ENSP00000507633.1:p.His172_Pro192del
ENST00000682772.1:c.-312_-250del	ENSP00000506848.1:n.-312_-250del
ENST00000683211.1:c.859_921del	ENSP00000508257.1:p.His287_Pro307del
ENST00000683250.1:c.404-16118_404-16056del	ENSP00000506847.1:n.404-16118_404-16056del
ENST00000683418.1:n.3206_3268del
ENST00000683678.1:n.859_921del
ENST00000684153.1:c.514_576del	ENSP00000506937.1:p.His172_Pro192del
ENST00000358487.10:c.859_921del MANE Select	ENSP00000351276.6:p.His287_Pro307del
ENST00000336553.10:c.592_654del	ENSP00000337665.6:p.His198_Pro218del
ENST00000346997.6:c.859_921del	ENSP00000263451.5:p.His287_Pro307del
ENST00000351936.10:c.859_921del	ENSP00000309878.9:p.His287_Pro307del
ENST00000356226.8:c.514_576del	ENSP00000348559.4:p.His172_Pro192del
ENST00000357555.9:c.592_654del	ENSP00000350166.5:p.His198_Pro218del
ENST00000358487.9:c.859_921del	ENSP00000351276.5:p.His287_Pro307del
ENST00000360144.7:c.592_654del	ENSP00000353262.3:p.His198_Pro218del
ENST00000369056.5:c.859_921del	ENSP00000358052.1:p.His287_Pro307del
ENST00000369058.7:c.859_921del	ENSP00000358054.3:p.His287_Pro307del
ENST00000369059.5:c.514_576del	ENSP00000358055.1:p.His172_Pro192del
ENST00000369060.8:c.859_921del	ENSP00000358056.4:p.His287_Pro307del
ENST00000369061.8:c.749-4740_749-4678del	ENSP00000358057.4:n.749-4740_749-4678del
ENST00000457416.6:c.859_921del	ENSP00000410294.2:p.His287_Pro307del
ENST00000478859.5:c.175_237del	ENSP00000474011.1:p.His59_Pro79del
ENST00000490349.5:n.1120_1182del
ENST00000604236.5:c.514_576del	ENSP00000474109.1:p.His172_Pro192del
ENST00000613048.4:c.592_654del	ENSP00000484154.1:p.His198_Pro218del
NM_000141.4:c.859_921del	NP_000132.3:p.His287_Pro307del
NM_001144913.1:c.859_921del	NP_001138385.1:p.His287_Pro307del
NM_001144914.1:c.749-4740_749-4678del	NP_001138386.1:n.749-4740_749-4678del
NM_001144915.1:c.592_654del	NP_001138387.1:p.His198_Pro218del
NM_001144916.1:c.514_576del	NP_001138388.1:p.His172_Pro192del
NM_001144917.1:c.859_921del	NP_001138389.1:p.His287_Pro307del
NM_001144918.1:c.514_576del	NP_001138390.1:p.His172_Pro192del
NM_001144919.1:c.592_654del	NP_001138391.1:p.His198_Pro218del
NM_022970.3:c.859_921del	NP_075259.4:p.His287_Pro307del
NM_023029.2:c.592_654del	NP_075418.1:p.His198_Pro218del
NR_073009.1:n.1161_1223del
XM_006717708.2:c.916_978del	XP_006717771.1:p.His306_Pro326del
XM_006717709.2:c.916_978del	XP_006717772.1:p.His306_Pro326del
XM_006717710.2:c.916_978del	XP_006717773.1:p.His306_Pro326del
XM_006717711.2:c.649_711del	XP_006717774.1:p.His217_Pro237del
XM_006717712.2:c.571_633del	XP_006717775.1:p.His191_Pro211del
XM_006717713.2:c.916_978del	XP_006717776.1:p.His306_Pro326del
XM_011539510.1:c.175_237del	XP_011537812.1:p.His59_Pro79del
NM_001320654.1:c.175_237del	NP_001307583.1:p.His59_Pro79del
NM_001320658.1:c.859_921del	NP_001307587.1:p.His287_Pro307del
XM_006717708.3:c.916_978del	XP_006717771.1:p.His306_Pro326del
XM_006717710.4:c.916_978del	XP_006717773.1:p.His306_Pro326del
XM_017015920.2:c.916_978del	XP_016871409.1:p.His306_Pro326del
XM_017015921.2:c.916_978del	XP_016871410.1:p.His306_Pro326del
XM_017015924.2:c.571_633del	XP_016871413.1:p.His191_Pro211del
XM_017015925.2:c.571_633del	XP_016871414.1:p.His191_Pro211del
XM_024447887.1:c.649_711del	XP_024303655.1:p.His217_Pro237del
XM_024447888.1:c.649_711del	XP_024303656.1:p.His217_Pro237del
XM_024447889.1:c.649_711del	XP_024303657.1:p.His217_Pro237del
XM_024447890.1:c.649_711del	XP_024303658.1:p.His217_Pro237del
XM_024447891.1:c.571_633del	XP_024303659.1:p.His191_Pro211del
XM_024447892.1:c.-312_-250del	XP_024303660.1:n.-312_-250del
NM_000141.5:c.859_921del MANE Select	NP_000132.3:p.His287_Pro307del
NM_001144917.2:c.859_921del	NP_001138389.1:p.His287_Pro307del
NM_001144918.2:c.514_576del	NP_001138390.1:p.His172_Pro192del
NM_001144919.2:c.592_654del	NP_001138391.1:p.His198_Pro218del
NM_001320658.2:c.859_921del	NP_001307587.1:p.His287_Pro307del
NR_073009.2:n.1147_1209del
NM_001144915.2:c.592_654del	NP_001138387.1:p.His198_Pro218del
NM_001144916.2:c.514_576del	NP_001138388.1:p.His172_Pro192del
NM_001320654.2:c.175_237del	NP_001307583.1:p.His59_Pro79del