Canonical Allele Identifier: CA378327039

Gene: FGFR2

Linked Data

• dbSNP Id: rs2134222663
• MyVariant Identifiers: chr10:g.123274682C>A (hg19) ; chr10:g.121515168C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121515168C>A , CM000672.2:g.121515168C>A	GRCh38
NC_000010.10:g.123274682C>A , CM000672.1:g.123274682C>A	GRCh37
NC_000010.9:g.123264672C>A	NCBI36
NG_012449.1:g.88291G>T
NG_012449.2:g.88291G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000457416.7:c.1239G>T MANE Plus Clinical	ENSP00000410294.2:p.Gln413His
ENST00000351936.11:c.1236G>T	ENSP00000309878.10:p.Gln412His
ENST00000638709.2:c.66G>T	ENSP00000491912.2:p.Gln22His
ENST00000682296.1:n.584G>T
ENST00000682550.1:c.891G>T	ENSP00000507633.1:p.Gln297His
ENST00000682772.1:c.66G>T	ENSP00000506848.1:p.Gln22His
ENST00000683211.1:c.1236G>T	ENSP00000508257.1:p.Gln412His
ENST00000683250.1:c.404-11227G>T	ENSP00000506847.1:n.404-11227G>T
ENST00000683418.1:n.3583G>T
ENST00000684153.1:c.891G>T	ENSP00000506937.1:p.Gln297His
ENST00000358487.10:c.1236G>T MANE Select	ENSP00000351276.6:p.Gln412His
ENST00000336553.10:c.969G>T	ENSP00000337665.6:p.Gln323His
ENST00000346997.6:c.1236G>T	ENSP00000263451.5:p.Gln412His
ENST00000351936.10:c.1242G>T	ENSP00000309878.9:p.Gln414His
ENST00000356226.8:c.891G>T	ENSP00000348559.4:p.Gln297His
ENST00000357555.9:c.969G>T	ENSP00000350166.5:p.Gln323His
ENST00000358487.9:c.1236G>T	ENSP00000351276.5:p.Gln412His
ENST00000360144.7:c.972G>T	ENSP00000353262.3:p.Gln324His
ENST00000369056.5:c.1239G>T	ENSP00000358052.1:p.Gln413His
ENST00000369058.7:c.1239G>T	ENSP00000358054.3:p.Gln413His
ENST00000369059.5:c.894G>T	ENSP00000358055.1:p.Gln298His
ENST00000369060.8:c.939+4811G>T	ENSP00000358056.4:n.939+4811G>T
ENST00000369061.8:c.900G>T	ENSP00000358057.4:p.Gln300His
ENST00000429361.5:c.12G>T	ENSP00000404219.1:p.Gln4His
ENST00000457416.6:c.1239G>T	ENSP00000410294.2:p.Gln413His
ENST00000478859.5:c.552G>T	ENSP00000474011.1:p.Gln184His
ENST00000604236.5:c.*283G>T	ENSP00000474109.1:n.*283G>T
ENST00000613048.4:c.969G>T	ENSP00000484154.1:p.Gln323His
NM_000141.4:c.1236G>T	NP_000132.3:p.Gln412His
NM_001144913.1:c.1239G>T	NP_001138385.1:p.Gln413His
NM_001144914.1:c.900G>T	NP_001138386.1:p.Gln300His
NM_001144915.1:c.969G>T	NP_001138387.1:p.Gln323His
NM_001144916.1:c.891G>T	NP_001138388.1:p.Gln297His
NM_001144917.1:c.939+4811G>T	NP_001138389.1:n.939+4811G>T
NM_001144918.1:c.891G>T	NP_001138390.1:p.Gln297His
NM_001144919.1:c.972G>T	NP_001138391.1:p.Gln324His
NM_022970.3:c.1239G>T	NP_075259.4:p.Gln413His
NM_023029.2:c.969G>T	NP_075418.1:p.Gln323His
NR_073009.1:n.1686G>T
XM_006717708.2:c.1296G>T	XP_006717771.1:p.Gln432His
XM_006717709.2:c.1293G>T	XP_006717772.1:p.Gln431His
XM_006717710.2:c.1296G>T	XP_006717773.1:p.Gln432His
XM_006717711.2:c.1029G>T	XP_006717774.1:p.Gln343His
XM_006717712.2:c.951G>T	XP_006717775.1:p.Gln317His
XM_006717713.2:c.1293G>T	XP_006717776.1:p.Gln431His
XM_011539510.1:c.552G>T	XP_011537812.1:p.Gln184His
NM_001320654.1:c.552G>T	NP_001307583.1:p.Gln184His
NM_001320658.1:c.1236G>T	NP_001307587.1:p.Gln412His
XM_006717708.3:c.1296G>T	XP_006717771.1:p.Gln432His
XM_006717710.4:c.1296G>T	XP_006717773.1:p.Gln432His
XM_017015920.2:c.1296G>T	XP_016871409.1:p.Gln432His
XM_017015921.2:c.1293G>T	XP_016871410.1:p.Gln431His
XM_017015924.2:c.948G>T	XP_016871413.1:p.Gln316His
XM_017015925.2:c.948G>T	XP_016871414.1:p.Gln316His
XM_024447887.1:c.1026G>T	XP_024303655.1:p.Gln342His
XM_024447888.1:c.1029G>T	XP_024303656.1:p.Gln343His
XM_024447889.1:c.1026G>T	XP_024303657.1:p.Gln342His
XM_024447890.1:c.1029G>T	XP_024303658.1:p.Gln343His
XM_024447891.1:c.951G>T	XP_024303659.1:p.Gln317His
XM_024447892.1:c.66G>T	XP_024303660.1:p.Gln22His
NM_000141.5:c.1236G>T MANE Select	NP_000132.3:p.Gln412His
NM_001144917.2:c.939+4811G>T	NP_001138389.1:n.939+4811G>T
NM_001144918.2:c.891G>T	NP_001138390.1:p.Gln297His
NM_001144919.2:c.972G>T	NP_001138391.1:p.Gln324His
NM_001320658.2:c.1236G>T	NP_001307587.1:p.Gln412His
NR_073009.2:n.1672G>T
NM_001144915.2:c.969G>T	NP_001138387.1:p.Gln323His
NM_001144916.2:c.891G>T	NP_001138388.1:p.Gln297His
NM_001320654.2:c.552G>T	NP_001307583.1:p.Gln184His