Canonical Allele Identifier: CA2611197651

Gene: FGFR2

Linked Data

• gnomAD v4: 10-121479384-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121479384G>T , CM000672.2:g.121479384G>T	GRCh38
NC_000010.10:g.123238898G>T , CM000672.1:g.123238898G>T	GRCh37
NC_000010.9:g.123228888G>T	NCBI36
NG_012449.1:g.124075C>A
NG_012449.2:g.124075C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000457416.7:c.*473C>A MANE Plus Clinical	ENSP00000410294.2:n.*473C>A
ENST00000351936.11:c.*473C>A	ENSP00000309878.10:n.*473C>A
ENST00000638709.2:c.*473C>A	ENSP00000491912.2:n.*473C>A
ENST00000682296.1:n.2281C>A
ENST00000682550.1:c.*473C>A	ENSP00000507633.1:n.*473C>A
ENST00000682772.1:c.*473C>A	ENSP00000506848.1:n.*473C>A
ENST00000682904.1:n.1759C>A
ENST00000683029.1:n.2942C>A
ENST00000683211.1:c.*473C>A	ENSP00000508257.1:n.*473C>A
ENST00000683250.1:c.*3232C>A	ENSP00000506847.1:n.*3232C>A
ENST00000683418.1:n.5280C>A
ENST00000684153.1:c.*667C>A	ENSP00000506937.1:n.*667C>A
ENST00000684516.1:n.3952C>A
ENST00000358487.10:c.*473C>A MANE Select	ENSP00000351276.6:n.*473C>A
ENST00000638709.1:c.926C>A
ENST00000356226.8:c.*473C>A	ENSP00000348559.4:n.*473C>A
ENST00000357555.9:c.*197C>A	ENSP00000350166.5:n.*197C>A
ENST00000358487.9:c.*473C>A	ENSP00000351276.5:n.*473C>A
ENST00000369060.8:c.*473C>A	ENSP00000358056.4:n.*473C>A
ENST00000369061.8:c.*473C>A	ENSP00000358057.4:n.*473C>A
ENST00000478859.5:c.*473C>A	ENSP00000474011.1:n.*473C>A
ENST00000604236.5:c.*1986C>A	ENSP00000474109.1:n.*1986C>A
ENST00000613048.4:c.*473C>A	ENSP00000484154.1:n.*473C>A
NM_000141.4:c.*473C>A	NP_000132.3:n.*473C>A
NM_001144914.1:c.*473C>A	NP_001138386.1:n.*473C>A
NM_001144915.1:c.*197C>A	NP_001138387.1:n.*197C>A
NM_001144916.1:c.*473C>A	NP_001138388.1:n.*473C>A
NM_001144917.1:c.*473C>A	NP_001138389.1:n.*473C>A
NM_001144918.1:c.*473C>A	NP_001138390.1:n.*473C>A
NM_022970.3:c.*473C>A	NP_075259.4:n.*473C>A
NM_023029.2:c.*473C>A	NP_075418.1:n.*473C>A
NR_073009.1:n.3389C>A
XM_006717708.2:c.*473C>A	XP_006717771.1:n.*473C>A
XM_006717709.2:c.*473C>A	XP_006717772.1:n.*473C>A
XM_006717711.2:c.*473C>A	XP_006717774.1:n.*473C>A
XM_006717712.2:c.*473C>A	XP_006717775.1:n.*473C>A
XM_011539510.1:c.*473C>A	XP_011537812.1:n.*473C>A
NM_001320654.1:c.*473C>A	NP_001307583.1:n.*473C>A
NM_001320658.1:c.*473C>A	NP_001307587.1:n.*473C>A
XM_006717708.3:c.*473C>A	XP_006717771.1:n.*473C>A
XM_006717710.4:c.*667C>A	XP_006717773.1:n.*667C>A
XM_017015920.2:c.*667C>A	XP_016871409.1:n.*667C>A
XM_017015921.2:c.*667C>A	XP_016871410.1:n.*667C>A
XM_017015924.2:c.*473C>A	XP_016871413.1:n.*473C>A
XM_017015925.2:c.*667C>A	XP_016871414.1:n.*667C>A
XM_024447887.1:c.*473C>A	XP_024303655.1:n.*473C>A
XM_024447888.1:c.*473C>A	XP_024303656.1:n.*473C>A
XM_024447889.1:c.*473C>A	XP_024303657.1:n.*473C>A
XM_024447890.1:c.*473C>A	XP_024303658.1:n.*473C>A
XM_024447891.1:c.*473C>A	XP_024303659.1:n.*473C>A
XM_024447892.1:c.*473C>A	XP_024303660.1:n.*473C>A
NM_000141.5:c.*473C>A MANE Select	NP_000132.3:n.*473C>A
NM_001144917.2:c.*473C>A	NP_001138389.1:n.*473C>A
NM_001144918.2:c.*473C>A	NP_001138390.1:n.*473C>A
NM_001320658.2:c.*473C>A	NP_001307587.1:n.*473C>A
NR_073009.2:n.3375C>A
NM_001144915.2:c.*197C>A	NP_001138387.1:n.*197C>A
NM_001144916.2:c.*473C>A	NP_001138388.1:n.*473C>A
NM_001320654.2:c.*473C>A	NP_001307583.1:n.*473C>A