Canonical Allele Identifier: CA2695212854

Gene: FGFR2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121520114_121520115insCCA , CM000672.2:g.121520114_121520115insCCA	GRCh38
NC_000010.10:g.123279628_123279629insCCA , CM000672.1:g.123279628_123279629insCCA	GRCh37
NC_000010.9:g.123269618_123269619insCCA	NCBI36
NG_012449.1:g.83344_83345insTGG
NG_012449.2:g.83344_83345insTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000457416.7:c.803_804insTGG MANE Plus Clinical	ENSP00000410294.2:p.Thr268_Val269insGly
ENST00000351936.11:c.803_804insTGG	ENSP00000309878.10:p.Thr268_Val269insGly
ENST00000638709.2:c.-368_-367insTGG	ENSP00000491912.2:n.-368_-367insTGG
ENST00000682296.1:n.151_152insTGG
ENST00000682400.1:n.458_459insTGG
ENST00000682550.1:c.458_459insTGG	ENSP00000507633.1:p.Thr153_Val154insGly
ENST00000682772.1:c.-368_-367insTGG	ENSP00000506848.1:n.-368_-367insTGG
ENST00000683211.1:c.803_804insTGG	ENSP00000508257.1:p.Thr268_Val269insGly
ENST00000683250.1:c.404-16174_404-16173insTGG	ENSP00000506847.1:n.404-16174_404-16173insTGG
ENST00000683418.1:n.3150_3151insTGG
ENST00000683678.1:n.803_804insTGG
ENST00000684153.1:c.458_459insTGG	ENSP00000506937.1:p.Thr153_Val154insGly
ENST00000358487.10:c.803_804insTGG MANE Select	ENSP00000351276.6:p.Thr268_Val269insGly
ENST00000336553.10:c.536_537insTGG	ENSP00000337665.6:p.Thr179_Val180insGly
ENST00000346997.6:c.803_804insTGG	ENSP00000263451.5:p.Thr268_Val269insGly
ENST00000351936.10:c.803_804insTGG	ENSP00000309878.9:p.Thr268_Val269insGly
ENST00000356226.8:c.458_459insTGG	ENSP00000348559.4:p.Thr153_Val154insGly
ENST00000357555.9:c.536_537insTGG	ENSP00000350166.5:p.Thr179_Val180insGly
ENST00000358487.9:c.803_804insTGG	ENSP00000351276.5:p.Thr268_Val269insGly
ENST00000360144.7:c.536_537insTGG	ENSP00000353262.3:p.Thr179_Val180insGly
ENST00000369056.5:c.803_804insTGG	ENSP00000358052.1:p.Thr268_Val269insGly
ENST00000369058.7:c.803_804insTGG	ENSP00000358054.3:p.Thr268_Val269insGly
ENST00000369059.5:c.458_459insTGG	ENSP00000358055.1:p.Thr153_Val154insGly
ENST00000369060.8:c.803_804insTGG	ENSP00000358056.4:p.Thr268_Val269insGly
ENST00000369061.8:c.749-4796_749-4795insTGG	ENSP00000358057.4:n.749-4796_749-4795insTGG
ENST00000457416.6:c.803_804insTGG	ENSP00000410294.2:p.Thr268_Val269insGly
ENST00000478859.5:c.119_120insTGG	ENSP00000474011.1:p.Thr40_Val41insGly
ENST00000490349.5:n.1064_1065insTGG
ENST00000604236.5:c.458_459insTGG	ENSP00000474109.1:p.Thr153_Val154insGly
ENST00000613048.4:c.536_537insTGG	ENSP00000484154.1:p.Thr179_Val180insGly
NM_000141.4:c.803_804insTGG	NP_000132.3:p.Thr268_Val269insGly
NM_001144913.1:c.803_804insTGG	NP_001138385.1:p.Thr268_Val269insGly
NM_001144914.1:c.749-4796_749-4795insTGG	NP_001138386.1:n.749-4796_749-4795insTGG
NM_001144915.1:c.536_537insTGG	NP_001138387.1:p.Thr179_Val180insGly
NM_001144916.1:c.458_459insTGG	NP_001138388.1:p.Thr153_Val154insGly
NM_001144917.1:c.803_804insTGG	NP_001138389.1:p.Thr268_Val269insGly
NM_001144918.1:c.458_459insTGG	NP_001138390.1:p.Thr153_Val154insGly
NM_001144919.1:c.536_537insTGG	NP_001138391.1:p.Thr179_Val180insGly
NM_022970.3:c.803_804insTGG	NP_075259.4:p.Thr268_Val269insGly
NM_023029.2:c.536_537insTGG	NP_075418.1:p.Thr179_Val180insGly
NR_073009.1:n.1105_1106insTGG
XM_006717708.2:c.860_861insTGG	XP_006717771.1:p.Thr287_Val288insGly
XM_006717709.2:c.860_861insTGG	XP_006717772.1:p.Thr287_Val288insGly
XM_006717710.2:c.860_861insTGG	XP_006717773.1:p.Thr287_Val288insGly
XM_006717711.2:c.593_594insTGG	XP_006717774.1:p.Thr198_Val199insGly
XM_006717712.2:c.515_516insTGG	XP_006717775.1:p.Thr172_Val173insGly
XM_006717713.2:c.860_861insTGG	XP_006717776.1:p.Thr287_Val288insGly
XM_011539510.1:c.119_120insTGG	XP_011537812.1:p.Thr40_Val41insGly
NM_001320654.1:c.119_120insTGG	NP_001307583.1:p.Thr40_Val41insGly
NM_001320658.1:c.803_804insTGG	NP_001307587.1:p.Thr268_Val269insGly
XM_006717708.3:c.860_861insTGG	XP_006717771.1:p.Thr287_Val288insGly
XM_006717710.4:c.860_861insTGG	XP_006717773.1:p.Thr287_Val288insGly
XM_017015920.2:c.860_861insTGG	XP_016871409.1:p.Thr287_Val288insGly
XM_017015921.2:c.860_861insTGG	XP_016871410.1:p.Thr287_Val288insGly
XM_017015924.2:c.515_516insTGG	XP_016871413.1:p.Thr172_Val173insGly
XM_017015925.2:c.515_516insTGG	XP_016871414.1:p.Thr172_Val173insGly
XM_024447887.1:c.593_594insTGG	XP_024303655.1:p.Thr198_Val199insGly
XM_024447888.1:c.593_594insTGG	XP_024303656.1:p.Thr198_Val199insGly
XM_024447889.1:c.593_594insTGG	XP_024303657.1:p.Thr198_Val199insGly
XM_024447890.1:c.593_594insTGG	XP_024303658.1:p.Thr198_Val199insGly
XM_024447891.1:c.515_516insTGG	XP_024303659.1:p.Thr172_Val173insGly
XM_024447892.1:c.-368_-367insTGG	XP_024303660.1:n.-368_-367insTGG
NM_000141.5:c.803_804insTGG MANE Select	NP_000132.3:p.Thr268_Val269insGly
NM_001144917.2:c.803_804insTGG	NP_001138389.1:p.Thr268_Val269insGly
NM_001144918.2:c.458_459insTGG	NP_001138390.1:p.Thr153_Val154insGly
NM_001144919.2:c.536_537insTGG	NP_001138391.1:p.Thr179_Val180insGly
NM_001320658.2:c.803_804insTGG	NP_001307587.1:p.Thr268_Val269insGly
NR_073009.2:n.1091_1092insTGG
NM_001144915.2:c.536_537insTGG	NP_001138387.1:p.Thr179_Val180insGly
NM_001144916.2:c.458_459insTGG	NP_001138388.1:p.Thr153_Val154insGly
NM_001320654.2:c.119_120insTGG	NP_001307583.1:p.Thr40_Val41insGly