Canonical Allele Identifier: CA1941012764

Gene: FGFR2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121488065T= , CM000672.2:g.121488065T=	GRCh38
NC_000010.10:g.123247579T= , CM000672.1:g.123247579T=	GRCh37
NC_000010.9:g.123237569T=	NCBI36
NG_012449.1:g.115394A=
NG_012449.2:g.115394A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000457416.7:c.1915A= MANE Plus Clinical	ENSP00000410294.2:p.Asn639=
ENST00000351936.11:c.1906A=	ENSP00000309878.10:p.Asn636=
ENST00000638709.2:c.736A=	ENSP00000491912.2:p.Asn246=
ENST00000682296.1:n.1254A=
ENST00000682550.1:c.1561A=	ENSP00000507633.1:p.Asn521=
ENST00000682772.1:c.736A=	ENSP00000506848.1:p.Asn246=
ENST00000682904.1:n.732A=
ENST00000683029.1:n.324A=
ENST00000683211.1:c.1906A=	ENSP00000508257.1:p.Asn636=
ENST00000683250.1:c.*614A=	ENSP00000506847.1:n.*614A=
ENST00000683418.1:n.4253A=
ENST00000684153.1:c.1561A=	ENSP00000506937.1:p.Asn521=
ENST00000684516.1:n.2925A=
ENST00000358487.10:c.1912A= MANE Select	ENSP00000351276.6:p.Asn638=
ENST00000336553.10:c.1639A=	ENSP00000337665.6:p.Asn547=
ENST00000346997.6:c.1906A=	ENSP00000263451.5:p.Asn636=
ENST00000351936.10:c.1912A=	ENSP00000309878.9:p.Asn638=
ENST00000356226.8:c.1561A=	ENSP00000348559.4:p.Asn521=
ENST00000357555.9:c.1645A=	ENSP00000350166.5:p.Asn549=
ENST00000358487.9:c.1912A=	ENSP00000351276.5:p.Asn638=
ENST00000360144.7:c.1648A=	ENSP00000353262.3:p.Asn550=
ENST00000369056.5:c.1915A=	ENSP00000358052.1:p.Asn639=
ENST00000369058.7:c.1915A=	ENSP00000358054.3:p.Asn639=
ENST00000369059.5:c.1570A=	ENSP00000358055.1:p.Asn524=
ENST00000369060.8:c.1564A=	ENSP00000358056.4:p.Asn522=
ENST00000369061.8:c.1576A=	ENSP00000358057.4:p.Asn526=
ENST00000429361.5:c.688A=	ENSP00000404219.1:p.Asn230=
ENST00000457416.6:c.1915A=	ENSP00000410294.2:p.Asn639=
ENST00000478859.5:c.1228A=	ENSP00000474011.1:p.Asn410=
ENST00000604236.5:c.*959A=	ENSP00000474109.1:n.*959A=
ENST00000613048.4:c.1645A=	ENSP00000484154.1:p.Asn549=
NM_000141.4:c.1912A=	NP_000132.3:p.Asn638=
NM_001144913.1:c.1915A=	NP_001138385.1:p.Asn639=
NM_001144914.1:c.1576A=	NP_001138386.1:p.Asn526=
NM_001144915.1:c.1645A=	NP_001138387.1:p.Asn549=
NM_001144916.1:c.1567A=	NP_001138388.1:p.Asn523=
NM_001144917.1:c.1564A=	NP_001138389.1:p.Asn522=
NM_001144918.1:c.1561A=	NP_001138390.1:p.Asn521=
NM_001144919.1:c.1648A=	NP_001138391.1:p.Asn550=
NM_022970.3:c.1915A=	NP_075259.4:p.Asn639=
NM_023029.2:c.1645A=	NP_075418.1:p.Asn549=
NR_073009.1:n.2362A=
XM_006717708.2:c.1966A=	XP_006717771.1:p.Asn656=
XM_006717709.2:c.1963A=	XP_006717772.1:p.Asn655=
XM_006717710.2:c.1972A=	XP_006717773.1:p.Asn658=
XM_006717711.2:c.1705A=	XP_006717774.1:p.Asn569=
XM_006717712.2:c.1627A=	XP_006717775.1:p.Asn543=
XM_006717713.2:c.1969A=	XP_006717776.1:p.Asn657=
XM_011539510.1:c.1228A=	XP_011537812.1:p.Asn410=
NM_001320654.1:c.1228A=	NP_001307583.1:p.Asn410=
NM_001320658.1:c.1906A=	NP_001307587.1:p.Asn636=
XM_006717708.3:c.1966A=	XP_006717771.1:p.Asn656=
XM_006717710.4:c.1972A=	XP_006717773.1:p.Asn658=
XM_017015920.2:c.1966A=	XP_016871409.1:p.Asn656=
XM_017015921.2:c.1963A=	XP_016871410.1:p.Asn655=
XM_017015924.2:c.1624A=	XP_016871413.1:p.Asn542=
XM_017015925.2:c.1618A=	XP_016871414.1:p.Asn540=
XM_024447887.1:c.1702A=	XP_024303655.1:p.Asn568=
XM_024447888.1:c.1699A=	XP_024303656.1:p.Asn567=
XM_024447889.1:c.1696A=	XP_024303657.1:p.Asn566=
XM_024447890.1:c.1705A=	XP_024303658.1:p.Asn569=
XM_024447891.1:c.1627A=	XP_024303659.1:p.Asn543=
XM_024447892.1:c.742A=	XP_024303660.1:p.Asn248=
NM_000141.5:c.1912A= MANE Select	NP_000132.3:p.Asn638=
NM_001144917.2:c.1564A=	NP_001138389.1:p.Asn522=
NM_001144918.2:c.1561A=	NP_001138390.1:p.Asn521=
NM_001144919.2:c.1648A=	NP_001138391.1:p.Asn550=
NM_001320658.2:c.1906A=	NP_001307587.1:p.Asn636=
NR_073009.2:n.2348A=
NM_001144915.2:c.1645A=	NP_001138387.1:p.Asn549=
NM_001144916.2:c.1567A=	NP_001138388.1:p.Asn523=
NM_001320654.2:c.1228A=	NP_001307583.1:p.Asn410=