Canonical Allele Identifier: CA378314919

Gene: FGFR2

Linked Data

• MyVariant Identifiers: chr10:g.123247599T>G (hg19) ; chr10:g.121488085T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121488085T>G , CM000672.2:g.121488085T>G	GRCh38
NC_000010.10:g.123247599T>G , CM000672.1:g.123247599T>G	GRCh37
NC_000010.9:g.123237589T>G	NCBI36
NG_012449.1:g.115374A>C
NG_012449.2:g.115374A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000457416.7:c.1895A>C MANE Plus Clinical	ENSP00000410294.2:p.Asn632Thr
ENST00000351936.11:c.1886A>C	ENSP00000309878.10:p.Asn629Thr
ENST00000638709.2:c.716A>C	ENSP00000491912.2:p.Asn239Thr
ENST00000682296.1:n.1234A>C
ENST00000682550.1:c.1541A>C	ENSP00000507633.1:p.Asn514Thr
ENST00000682772.1:c.716A>C	ENSP00000506848.1:p.Asn239Thr
ENST00000682904.1:n.712A>C
ENST00000683029.1:n.304A>C
ENST00000683211.1:c.1886A>C	ENSP00000508257.1:p.Asn629Thr
ENST00000683250.1:c.*594A>C	ENSP00000506847.1:n.*594A>C
ENST00000683418.1:n.4233A>C
ENST00000684153.1:c.1541A>C	ENSP00000506937.1:p.Asn514Thr
ENST00000684516.1:n.2905A>C
ENST00000358487.10:c.1892A>C MANE Select	ENSP00000351276.6:p.Asn631Thr
ENST00000336553.10:c.1619A>C	ENSP00000337665.6:p.Asn540Thr
ENST00000346997.6:c.1886A>C	ENSP00000263451.5:p.Asn629Thr
ENST00000351936.10:c.1892A>C	ENSP00000309878.9:p.Asn631Thr
ENST00000356226.8:c.1541A>C	ENSP00000348559.4:p.Asn514Thr
ENST00000357555.9:c.1625A>C	ENSP00000350166.5:p.Asn542Thr
ENST00000358487.9:c.1892A>C	ENSP00000351276.5:p.Asn631Thr
ENST00000360144.7:c.1628A>C	ENSP00000353262.3:p.Asn543Thr
ENST00000369056.5:c.1895A>C	ENSP00000358052.1:p.Asn632Thr
ENST00000369058.7:c.1895A>C	ENSP00000358054.3:p.Asn632Thr
ENST00000369059.5:c.1550A>C	ENSP00000358055.1:p.Asn517Thr
ENST00000369060.8:c.1544A>C	ENSP00000358056.4:p.Asn515Thr
ENST00000369061.8:c.1556A>C	ENSP00000358057.4:p.Asn519Thr
ENST00000429361.5:c.668A>C	ENSP00000404219.1:p.Asn223Thr
ENST00000457416.6:c.1895A>C	ENSP00000410294.2:p.Asn632Thr
ENST00000478859.5:c.1208A>C	ENSP00000474011.1:p.Asn403Thr
ENST00000604236.5:c.*939A>C	ENSP00000474109.1:n.*939A>C
ENST00000613048.4:c.1625A>C	ENSP00000484154.1:p.Asn542Thr
NM_000141.4:c.1892A>C	NP_000132.3:p.Asn631Thr
NM_001144913.1:c.1895A>C	NP_001138385.1:p.Asn632Thr
NM_001144914.1:c.1556A>C	NP_001138386.1:p.Asn519Thr
NM_001144915.1:c.1625A>C	NP_001138387.1:p.Asn542Thr
NM_001144916.1:c.1547A>C	NP_001138388.1:p.Asn516Thr
NM_001144917.1:c.1544A>C	NP_001138389.1:p.Asn515Thr
NM_001144918.1:c.1541A>C	NP_001138390.1:p.Asn514Thr
NM_001144919.1:c.1628A>C	NP_001138391.1:p.Asn543Thr
NM_022970.3:c.1895A>C	NP_075259.4:p.Asn632Thr
NM_023029.2:c.1625A>C	NP_075418.1:p.Asn542Thr
NR_073009.1:n.2342A>C
XM_006717708.2:c.1946A>C	XP_006717771.1:p.Asn649Thr
XM_006717709.2:c.1943A>C	XP_006717772.1:p.Asn648Thr
XM_006717710.2:c.1952A>C	XP_006717773.1:p.Asn651Thr
XM_006717711.2:c.1685A>C	XP_006717774.1:p.Asn562Thr
XM_006717712.2:c.1607A>C	XP_006717775.1:p.Asn536Thr
XM_006717713.2:c.1949A>C	XP_006717776.1:p.Asn650Thr
XM_011539510.1:c.1208A>C	XP_011537812.1:p.Asn403Thr
NM_001320654.1:c.1208A>C	NP_001307583.1:p.Asn403Thr
NM_001320658.1:c.1886A>C	NP_001307587.1:p.Asn629Thr
XM_006717708.3:c.1946A>C	XP_006717771.1:p.Asn649Thr
XM_006717710.4:c.1952A>C	XP_006717773.1:p.Asn651Thr
XM_017015920.2:c.1946A>C	XP_016871409.1:p.Asn649Thr
XM_017015921.2:c.1943A>C	XP_016871410.1:p.Asn648Thr
XM_017015924.2:c.1604A>C	XP_016871413.1:p.Asn535Thr
XM_017015925.2:c.1598A>C	XP_016871414.1:p.Asn533Thr
XM_024447887.1:c.1682A>C	XP_024303655.1:p.Asn561Thr
XM_024447888.1:c.1679A>C	XP_024303656.1:p.Asn560Thr
XM_024447889.1:c.1676A>C	XP_024303657.1:p.Asn559Thr
XM_024447890.1:c.1685A>C	XP_024303658.1:p.Asn562Thr
XM_024447891.1:c.1607A>C	XP_024303659.1:p.Asn536Thr
XM_024447892.1:c.722A>C	XP_024303660.1:p.Asn241Thr
NM_000141.5:c.1892A>C MANE Select	NP_000132.3:p.Asn631Thr
NM_001144917.2:c.1544A>C	NP_001138389.1:p.Asn515Thr
NM_001144918.2:c.1541A>C	NP_001138390.1:p.Asn514Thr
NM_001144919.2:c.1628A>C	NP_001138391.1:p.Asn543Thr
NM_001320658.2:c.1886A>C	NP_001307587.1:p.Asn629Thr
NR_073009.2:n.2328A>C
NM_001144915.2:c.1625A>C	NP_001138387.1:p.Asn542Thr
NM_001144916.2:c.1547A>C	NP_001138388.1:p.Asn516Thr
NM_001320654.2:c.1208A>C	NP_001307583.1:p.Asn403Thr