Canonical Allele Identifier: CA471655998

Gene: FGFR2

Linked Data

• dbSNP Id: rs2134307276
• MyVariant Identifiers: chr10:g.123279499A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121519985A>T , CM000672.2:g.121519985A>T	GRCh38
NC_000010.10:g.123279499A>T , CM000672.1:g.123279499A>T	GRCh37
NC_000010.9:g.123269489A>T	NCBI36
NG_012449.1:g.83474T>A
NG_012449.2:g.83474T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000457416.7:c.933T>A MANE Plus Clinical	ENSP00000410294.2:p.Val311=
ENST00000351936.11:c.933T>A	ENSP00000309878.10:p.Val311=
ENST00000638709.2:c.-238T>A	ENSP00000491912.2:n.-238T>A
ENST00000682296.1:n.281T>A
ENST00000682400.1:n.588T>A
ENST00000682550.1:c.588T>A	ENSP00000507633.1:p.Val196=
ENST00000682772.1:c.-238T>A	ENSP00000506848.1:n.-238T>A
ENST00000683211.1:c.933T>A	ENSP00000508257.1:p.Val311=
ENST00000683250.1:c.404-16044T>A	ENSP00000506847.1:n.404-16044T>A
ENST00000683418.1:n.3280T>A
ENST00000683678.1:n.933T>A
ENST00000684153.1:c.588T>A	ENSP00000506937.1:p.Val196=
ENST00000358487.10:c.933T>A MANE Select	ENSP00000351276.6:p.Val311=
ENST00000336553.10:c.666T>A	ENSP00000337665.6:p.Val222=
ENST00000346997.6:c.933T>A	ENSP00000263451.5:p.Val311=
ENST00000351936.10:c.933T>A	ENSP00000309878.9:p.Val311=
ENST00000356226.8:c.588T>A	ENSP00000348559.4:p.Val196=
ENST00000357555.9:c.666T>A	ENSP00000350166.5:p.Val222=
ENST00000358487.9:c.933T>A	ENSP00000351276.5:p.Val311=
ENST00000360144.7:c.666T>A	ENSP00000353262.3:p.Val222=
ENST00000369056.5:c.933T>A	ENSP00000358052.1:p.Val311=
ENST00000369058.7:c.933T>A	ENSP00000358054.3:p.Val311=
ENST00000369059.5:c.588T>A	ENSP00000358055.1:p.Val196=
ENST00000369060.8:c.933T>A	ENSP00000358056.4:p.Val311=
ENST00000369061.8:c.749-4666T>A	ENSP00000358057.4:n.749-4666T>A
ENST00000457416.6:c.933T>A	ENSP00000410294.2:p.Val311=
ENST00000478859.5:c.249T>A	ENSP00000474011.1:p.Val83=
ENST00000490349.5:n.1194T>A
ENST00000604236.5:c.588T>A	ENSP00000474109.1:p.Val196=
ENST00000613048.4:c.666T>A	ENSP00000484154.1:p.Val222=
NM_000141.4:c.933T>A	NP_000132.3:p.Val311=
NM_001144913.1:c.933T>A	NP_001138385.1:p.Val311=
NM_001144914.1:c.749-4666T>A	NP_001138386.1:n.749-4666T>A
NM_001144915.1:c.666T>A	NP_001138387.1:p.Val222=
NM_001144916.1:c.588T>A	NP_001138388.1:p.Val196=
NM_001144917.1:c.933T>A	NP_001138389.1:p.Val311=
NM_001144918.1:c.588T>A	NP_001138390.1:p.Val196=
NM_001144919.1:c.666T>A	NP_001138391.1:p.Val222=
NM_022970.3:c.933T>A	NP_075259.4:p.Val311=
NM_023029.2:c.666T>A	NP_075418.1:p.Val222=
NR_073009.1:n.1235T>A
XM_006717708.2:c.990T>A	XP_006717771.1:p.Val330=
XM_006717709.2:c.990T>A	XP_006717772.1:p.Val330=
XM_006717710.2:c.990T>A	XP_006717773.1:p.Val330=
XM_006717711.2:c.723T>A	XP_006717774.1:p.Val241=
XM_006717712.2:c.645T>A	XP_006717775.1:p.Val215=
XM_006717713.2:c.990T>A	XP_006717776.1:p.Val330=
XM_011539510.1:c.249T>A	XP_011537812.1:p.Val83=
NM_001320654.1:c.249T>A	NP_001307583.1:p.Val83=
NM_001320658.1:c.933T>A	NP_001307587.1:p.Val311=
XM_006717708.3:c.990T>A	XP_006717771.1:p.Val330=
XM_006717710.4:c.990T>A	XP_006717773.1:p.Val330=
XM_017015920.2:c.990T>A	XP_016871409.1:p.Val330=
XM_017015921.2:c.990T>A	XP_016871410.1:p.Val330=
XM_017015924.2:c.645T>A	XP_016871413.1:p.Val215=
XM_017015925.2:c.645T>A	XP_016871414.1:p.Val215=
XM_024447887.1:c.723T>A	XP_024303655.1:p.Val241=
XM_024447888.1:c.723T>A	XP_024303656.1:p.Val241=
XM_024447889.1:c.723T>A	XP_024303657.1:p.Val241=
XM_024447890.1:c.723T>A	XP_024303658.1:p.Val241=
XM_024447891.1:c.645T>A	XP_024303659.1:p.Val215=
XM_024447892.1:c.-238T>A	XP_024303660.1:n.-238T>A
NM_000141.5:c.933T>A MANE Select	NP_000132.3:p.Val311=
NM_001144917.2:c.933T>A	NP_001138389.1:p.Val311=
NM_001144918.2:c.588T>A	NP_001138390.1:p.Val196=
NM_001144919.2:c.666T>A	NP_001138391.1:p.Val222=
NM_001320658.2:c.933T>A	NP_001307587.1:p.Val311=
NR_073009.2:n.1221T>A
NM_001144915.2:c.666T>A	NP_001138387.1:p.Val222=
NM_001144916.2:c.588T>A	NP_001138388.1:p.Val196=
NM_001320654.2:c.249T>A	NP_001307583.1:p.Val83=