Canonical Allele Identifier: CA471649381

Gene: FGFR2

Linked Data

• MyVariant Identifiers: chr10:g.123258034A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121498520A>G , CM000672.2:g.121498520A>G	GRCh38
NC_000010.10:g.123258034A>G , CM000672.1:g.123258034A>G	GRCh37
NC_000010.9:g.123248024A>G	NCBI36
NG_012449.1:g.104939T>C
NG_012449.2:g.104939T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000457416.7:c.1650T>C MANE Plus Clinical	ENSP00000410294.2:p.Asn550=
ENST00000351936.11:c.1641T>C	ENSP00000309878.10:p.Asn547=
ENST00000638709.2:c.471T>C	ENSP00000491912.2:p.Asn157=
ENST00000682296.1:n.989T>C
ENST00000682550.1:c.1296T>C	ENSP00000507633.1:p.Asn432=
ENST00000682772.1:c.471T>C	ENSP00000506848.1:p.Asn157=
ENST00000682904.1:n.467T>C
ENST00000683211.1:c.1641T>C	ENSP00000508257.1:p.Asn547=
ENST00000683250.1:c.*349T>C	ENSP00000506847.1:n.*349T>C
ENST00000683418.1:n.3988T>C
ENST00000684153.1:c.1296T>C	ENSP00000506937.1:p.Asn432=
ENST00000684516.1:n.2660T>C
ENST00000358487.10:c.1647T>C MANE Select	ENSP00000351276.6:p.Asn549=
ENST00000336553.10:c.1374T>C	ENSP00000337665.6:p.Asn458=
ENST00000346997.6:c.1641T>C	ENSP00000263451.5:p.Asn547=
ENST00000351936.10:c.1647T>C	ENSP00000309878.9:p.Asn549=
ENST00000356226.8:c.1296T>C	ENSP00000348559.4:p.Asn432=
ENST00000357555.9:c.1380T>C	ENSP00000350166.5:p.Asn460=
ENST00000358487.9:c.1647T>C	ENSP00000351276.5:p.Asn549=
ENST00000360144.7:c.1383T>C	ENSP00000353262.3:p.Asn461=
ENST00000369056.5:c.1650T>C	ENSP00000358052.1:p.Asn550=
ENST00000369058.7:c.1650T>C	ENSP00000358054.3:p.Asn550=
ENST00000369059.5:c.1305T>C	ENSP00000358055.1:p.Asn435=
ENST00000369060.8:c.1299T>C	ENSP00000358056.4:p.Asn433=
ENST00000369061.8:c.1311T>C	ENSP00000358057.4:p.Asn437=
ENST00000429361.5:c.423T>C	ENSP00000404219.1:p.Asn141=
ENST00000457416.6:c.1650T>C	ENSP00000410294.2:p.Asn550=
ENST00000478859.5:c.963T>C	ENSP00000474011.1:p.Asn321=
ENST00000604236.5:c.*694T>C	ENSP00000474109.1:n.*694T>C
ENST00000613048.4:c.1380T>C	ENSP00000484154.1:p.Asn460=
NM_000141.4:c.1647T>C	NP_000132.3:p.Asn549=
NM_001144913.1:c.1650T>C	NP_001138385.1:p.Asn550=
NM_001144914.1:c.1311T>C	NP_001138386.1:p.Asn437=
NM_001144915.1:c.1380T>C	NP_001138387.1:p.Asn460=
NM_001144916.1:c.1302T>C	NP_001138388.1:p.Asn434=
NM_001144917.1:c.1299T>C	NP_001138389.1:p.Asn433=
NM_001144918.1:c.1296T>C	NP_001138390.1:p.Asn432=
NM_001144919.1:c.1383T>C	NP_001138391.1:p.Asn461=
NM_022970.3:c.1650T>C	NP_075259.4:p.Asn550=
NM_023029.2:c.1380T>C	NP_075418.1:p.Asn460=
NR_073009.1:n.2097T>C
XM_006717708.2:c.1701T>C	XP_006717771.1:p.Asn567=
XM_006717709.2:c.1698T>C	XP_006717772.1:p.Asn566=
XM_006717710.2:c.1707T>C	XP_006717773.1:p.Asn569=
XM_006717711.2:c.1440T>C	XP_006717774.1:p.Asn480=
XM_006717712.2:c.1362T>C	XP_006717775.1:p.Asn454=
XM_006717713.2:c.1704T>C	XP_006717776.1:p.Asn568=
XM_011539510.1:c.963T>C	XP_011537812.1:p.Asn321=
NM_001320654.1:c.963T>C	NP_001307583.1:p.Asn321=
NM_001320658.1:c.1641T>C	NP_001307587.1:p.Asn547=
XM_006717708.3:c.1701T>C	XP_006717771.1:p.Asn567=
XM_006717710.4:c.1707T>C	XP_006717773.1:p.Asn569=
XM_017015920.2:c.1701T>C	XP_016871409.1:p.Asn567=
XM_017015921.2:c.1698T>C	XP_016871410.1:p.Asn566=
XM_017015924.2:c.1359T>C	XP_016871413.1:p.Asn453=
XM_017015925.2:c.1353T>C	XP_016871414.1:p.Asn451=
XM_024447887.1:c.1437T>C	XP_024303655.1:p.Asn479=
XM_024447888.1:c.1434T>C	XP_024303656.1:p.Asn478=
XM_024447889.1:c.1431T>C	XP_024303657.1:p.Asn477=
XM_024447890.1:c.1440T>C	XP_024303658.1:p.Asn480=
XM_024447891.1:c.1362T>C	XP_024303659.1:p.Asn454=
XM_024447892.1:c.477T>C	XP_024303660.1:p.Asn159=
NM_000141.5:c.1647T>C MANE Select	NP_000132.3:p.Asn549=
NM_001144917.2:c.1299T>C	NP_001138389.1:p.Asn433=
NM_001144918.2:c.1296T>C	NP_001138390.1:p.Asn432=
NM_001144919.2:c.1383T>C	NP_001138391.1:p.Asn461=
NM_001320658.2:c.1641T>C	NP_001307587.1:p.Asn547=
NR_073009.2:n.2083T>C
NM_001144915.2:c.1380T>C	NP_001138387.1:p.Asn460=
NM_001144916.2:c.1302T>C	NP_001138388.1:p.Asn434=
NM_001320654.2:c.963T>C	NP_001307583.1:p.Asn321=