Canonical Allele Identifier: CA378314525

Gene: FGFR2

Linked Data

• MyVariant Identifiers: chr10:g.123247551A>C (hg19) ; chr10:g.121488037A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121488037A>C , CM000672.2:g.121488037A>C	GRCh38
NC_000010.10:g.123247551A>C , CM000672.1:g.123247551A>C	GRCh37
NC_000010.9:g.123237541A>C	NCBI36
NG_012449.1:g.115422T>G
NG_012449.2:g.115422T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000457416.7:c.1943T>G MANE Plus Clinical	ENSP00000410294.2:p.Leu648Arg
ENST00000351936.11:c.1934T>G	ENSP00000309878.10:p.Leu645Arg
ENST00000638709.2:c.764T>G	ENSP00000491912.2:p.Leu255Arg
ENST00000682296.1:n.1282T>G
ENST00000682550.1:c.1589T>G	ENSP00000507633.1:p.Leu530Arg
ENST00000682772.1:c.764T>G	ENSP00000506848.1:p.Leu255Arg
ENST00000682904.1:n.760T>G
ENST00000683029.1:n.352T>G
ENST00000683211.1:c.1934T>G	ENSP00000508257.1:p.Leu645Arg
ENST00000683250.1:c.*642T>G	ENSP00000506847.1:n.*642T>G
ENST00000683418.1:n.4281T>G
ENST00000684153.1:c.1589T>G	ENSP00000506937.1:p.Leu530Arg
ENST00000684516.1:n.2953T>G
ENST00000358487.10:c.1940T>G MANE Select	ENSP00000351276.6:p.Leu647Arg
ENST00000336553.10:c.1667T>G	ENSP00000337665.6:p.Leu556Arg
ENST00000346997.6:c.1934T>G	ENSP00000263451.5:p.Leu645Arg
ENST00000351936.10:c.1940T>G	ENSP00000309878.9:p.Leu647Arg
ENST00000356226.8:c.1589T>G	ENSP00000348559.4:p.Leu530Arg
ENST00000357555.9:c.1673T>G	ENSP00000350166.5:p.Leu558Arg
ENST00000358487.9:c.1940T>G	ENSP00000351276.5:p.Leu647Arg
ENST00000360144.7:c.1676T>G	ENSP00000353262.3:p.Leu559Arg
ENST00000369056.5:c.1943T>G	ENSP00000358052.1:p.Leu648Arg
ENST00000369058.7:c.1943T>G	ENSP00000358054.3:p.Leu648Arg
ENST00000369059.5:c.1598T>G	ENSP00000358055.1:p.Leu533Arg
ENST00000369060.8:c.1592T>G	ENSP00000358056.4:p.Leu531Arg
ENST00000369061.8:c.1604T>G	ENSP00000358057.4:p.Leu535Arg
ENST00000429361.5:c.716T>G	ENSP00000404219.1:p.Leu239Arg
ENST00000457416.6:c.1943T>G	ENSP00000410294.2:p.Leu648Arg
ENST00000478859.5:c.1256T>G	ENSP00000474011.1:p.Leu419Arg
ENST00000604236.5:c.*987T>G	ENSP00000474109.1:n.*987T>G
ENST00000613048.4:c.1673T>G	ENSP00000484154.1:p.Leu558Arg
NM_000141.4:c.1940T>G	NP_000132.3:p.Leu647Arg
NM_001144913.1:c.1943T>G	NP_001138385.1:p.Leu648Arg
NM_001144914.1:c.1604T>G	NP_001138386.1:p.Leu535Arg
NM_001144915.1:c.1673T>G	NP_001138387.1:p.Leu558Arg
NM_001144916.1:c.1595T>G	NP_001138388.1:p.Leu532Arg
NM_001144917.1:c.1592T>G	NP_001138389.1:p.Leu531Arg
NM_001144918.1:c.1589T>G	NP_001138390.1:p.Leu530Arg
NM_001144919.1:c.1676T>G	NP_001138391.1:p.Leu559Arg
NM_022970.3:c.1943T>G	NP_075259.4:p.Leu648Arg
NM_023029.2:c.1673T>G	NP_075418.1:p.Leu558Arg
NR_073009.1:n.2390T>G
XM_006717708.2:c.1994T>G	XP_006717771.1:p.Leu665Arg
XM_006717709.2:c.1991T>G	XP_006717772.1:p.Leu664Arg
XM_006717710.2:c.2000T>G	XP_006717773.1:p.Leu667Arg
XM_006717711.2:c.1733T>G	XP_006717774.1:p.Leu578Arg
XM_006717712.2:c.1655T>G	XP_006717775.1:p.Leu552Arg
XM_006717713.2:c.1997T>G	XP_006717776.1:p.Leu666Arg
XM_011539510.1:c.1256T>G	XP_011537812.1:p.Leu419Arg
NM_001320654.1:c.1256T>G	NP_001307583.1:p.Leu419Arg
NM_001320658.1:c.1934T>G	NP_001307587.1:p.Leu645Arg
XM_006717708.3:c.1994T>G	XP_006717771.1:p.Leu665Arg
XM_006717710.4:c.2000T>G	XP_006717773.1:p.Leu667Arg
XM_017015920.2:c.1994T>G	XP_016871409.1:p.Leu665Arg
XM_017015921.2:c.1991T>G	XP_016871410.1:p.Leu664Arg
XM_017015924.2:c.1652T>G	XP_016871413.1:p.Leu551Arg
XM_017015925.2:c.1646T>G	XP_016871414.1:p.Leu549Arg
XM_024447887.1:c.1730T>G	XP_024303655.1:p.Leu577Arg
XM_024447888.1:c.1727T>G	XP_024303656.1:p.Leu576Arg
XM_024447889.1:c.1724T>G	XP_024303657.1:p.Leu575Arg
XM_024447890.1:c.1733T>G	XP_024303658.1:p.Leu578Arg
XM_024447891.1:c.1655T>G	XP_024303659.1:p.Leu552Arg
XM_024447892.1:c.770T>G	XP_024303660.1:p.Leu257Arg
NM_000141.5:c.1940T>G MANE Select	NP_000132.3:p.Leu647Arg
NM_001144917.2:c.1592T>G	NP_001138389.1:p.Leu531Arg
NM_001144918.2:c.1589T>G	NP_001138390.1:p.Leu530Arg
NM_001144919.2:c.1676T>G	NP_001138391.1:p.Leu559Arg
NM_001320658.2:c.1934T>G	NP_001307587.1:p.Leu645Arg
NR_073009.2:n.2376T>G
NM_001144915.2:c.1673T>G	NP_001138387.1:p.Leu558Arg
NM_001144916.2:c.1595T>G	NP_001138388.1:p.Leu532Arg
NM_001320654.2:c.1256T>G	NP_001307583.1:p.Leu419Arg