Canonical Allele Identifier: CA2531456477
Gene: FGFR2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121479362_121479363insATATTTACAATATAT , CM000672.2:g.121479362_121479363insATATTTACAATATAT GRCh38
NC_000010.10:g.123238876_123238877insATATTTACAATATAT , CM000672.1:g.123238876_123238877insATATTTACAATATAT GRCh37
NC_000010.9:g.123228866_123228867insATATTTACAATATAT NCBI36
NG_012449.1:g.124096_124097insATATATTGTAAATAT
NG_012449.2:g.124096_124097insATATATTGTAAATAT

Transcript Alleles

HGVS Amino-acid change
ENST00000457416.7:c.*494_*495insATATATTGTAAATAT MANE Plus Clinical ENSP00000410294.2:n.*494_*495insATATATTGTAAATAT
ENST00000351936.11:c.*494_*495insATATATTGTAAATAT ENSP00000309878.10:n.*494_*495insATATATTGTAAATAT
ENST00000638709.2:c.*494_*495insATATATTGTAAATAT ENSP00000491912.2:n.*494_*495insATATATTGTAAATAT
ENST00000682296.1:n.2302_2303insATATATTGTAAATAT
ENST00000682550.1:c.*494_*495insATATATTGTAAATAT ENSP00000507633.1:n.*494_*495insATATATTGTAAATAT
ENST00000682772.1:c.*494_*495insATATATTGTAAATAT ENSP00000506848.1:n.*494_*495insATATATTGTAAATAT
ENST00000682904.1:n.1780_1781insATATATTGTAAATAT
ENST00000683029.1:n.2963_2964insATATATTGTAAATAT
ENST00000683211.1:c.*494_*495insATATATTGTAAATAT ENSP00000508257.1:n.*494_*495insATATATTGTAAATAT
ENST00000683250.1:c.*3253_*3254insATATATTGTAAATAT ENSP00000506847.1:n.*3253_*3254insATATATTGTAAATAT
ENST00000683418.1:n.5301_5302insATATATTGTAAATAT
ENST00000684153.1:c.*688_*689insATATATTGTAAATAT ENSP00000506937.1:n.*688_*689insATATATTGTAAATAT
ENST00000684516.1:n.3973_3974insATATATTGTAAATAT
ENST00000358487.10:c.*494_*495insATATATTGTAAATAT MANE Select ENSP00000351276.6:n.*494_*495insATATATTGTAAATAT
ENST00000638709.1:c.947_948insATATATTGTAAATAT
ENST00000356226.8:c.*494_*495insATATATTGTAAATAT ENSP00000348559.4:n.*494_*495insATATATTGTAAATAT
ENST00000357555.9:c.*218_*219insATATATTGTAAATAT ENSP00000350166.5:n.*218_*219insATATATTGTAAATAT
ENST00000358487.9:c.*494_*495insATATATTGTAAATAT ENSP00000351276.5:n.*494_*495insATATATTGTAAATAT
ENST00000369060.8:c.*494_*495insATATATTGTAAATAT ENSP00000358056.4:n.*494_*495insATATATTGTAAATAT
ENST00000369061.8:c.*494_*495insATATATTGTAAATAT ENSP00000358057.4:n.*494_*495insATATATTGTAAATAT
ENST00000478859.5:c.*494_*495insATATATTGTAAATAT ENSP00000474011.1:n.*494_*495insATATATTGTAAATAT
ENST00000604236.5:c.*2007_*2008insATATATTGTAAATAT ENSP00000474109.1:n.*2007_*2008insATATATTGTAAATAT
ENST00000613048.4:c.*494_*495insATATATTGTAAATAT ENSP00000484154.1:n.*494_*495insATATATTGTAAATAT
NM_000141.4:c.*494_*495insATATATTGTAAATAT NP_000132.3:n.*494_*495insATATATTGTAAATAT
NM_001144914.1:c.*494_*495insATATATTGTAAATAT NP_001138386.1:n.*494_*495insATATATTGTAAATAT
NM_001144915.1:c.*218_*219insATATATTGTAAATAT NP_001138387.1:n.*218_*219insATATATTGTAAATAT
NM_001144916.1:c.*494_*495insATATATTGTAAATAT NP_001138388.1:n.*494_*495insATATATTGTAAATAT
NM_001144917.1:c.*494_*495insATATATTGTAAATAT NP_001138389.1:n.*494_*495insATATATTGTAAATAT
NM_001144918.1:c.*494_*495insATATATTGTAAATAT NP_001138390.1:n.*494_*495insATATATTGTAAATAT
NM_022970.3:c.*494_*495insATATATTGTAAATAT NP_075259.4:n.*494_*495insATATATTGTAAATAT
NM_023029.2:c.*494_*495insATATATTGTAAATAT NP_075418.1:n.*494_*495insATATATTGTAAATAT
NR_073009.1:n.3410_3411insATATATTGTAAATAT
XM_006717708.2:c.*494_*495insATATATTGTAAATAT XP_006717771.1:n.*494_*495insATATATTGTAAATAT
XM_006717709.2:c.*494_*495insATATATTGTAAATAT XP_006717772.1:n.*494_*495insATATATTGTAAATAT
XM_006717711.2:c.*494_*495insATATATTGTAAATAT XP_006717774.1:n.*494_*495insATATATTGTAAATAT
XM_006717712.2:c.*494_*495insATATATTGTAAATAT XP_006717775.1:n.*494_*495insATATATTGTAAATAT
XM_011539510.1:c.*494_*495insATATATTGTAAATAT XP_011537812.1:n.*494_*495insATATATTGTAAATAT
NM_001320654.1:c.*494_*495insATATATTGTAAATAT NP_001307583.1:n.*494_*495insATATATTGTAAATAT
NM_001320658.1:c.*494_*495insATATATTGTAAATAT NP_001307587.1:n.*494_*495insATATATTGTAAATAT
XM_006717708.3:c.*494_*495insATATATTGTAAATAT XP_006717771.1:n.*494_*495insATATATTGTAAATAT
XM_006717710.4:c.*688_*689insATATATTGTAAATAT XP_006717773.1:n.*688_*689insATATATTGTAAATAT
XM_017015920.2:c.*688_*689insATATATTGTAAATAT XP_016871409.1:n.*688_*689insATATATTGTAAATAT
XM_017015921.2:c.*688_*689insATATATTGTAAATAT XP_016871410.1:n.*688_*689insATATATTGTAAATAT
XM_017015924.2:c.*494_*495insATATATTGTAAATAT XP_016871413.1:n.*494_*495insATATATTGTAAATAT
XM_017015925.2:c.*688_*689insATATATTGTAAATAT XP_016871414.1:n.*688_*689insATATATTGTAAATAT
XM_024447887.1:c.*494_*495insATATATTGTAAATAT XP_024303655.1:n.*494_*495insATATATTGTAAATAT
XM_024447888.1:c.*494_*495insATATATTGTAAATAT XP_024303656.1:n.*494_*495insATATATTGTAAATAT
XM_024447889.1:c.*494_*495insATATATTGTAAATAT XP_024303657.1:n.*494_*495insATATATTGTAAATAT
XM_024447890.1:c.*494_*495insATATATTGTAAATAT XP_024303658.1:n.*494_*495insATATATTGTAAATAT
XM_024447891.1:c.*494_*495insATATATTGTAAATAT XP_024303659.1:n.*494_*495insATATATTGTAAATAT
XM_024447892.1:c.*494_*495insATATATTGTAAATAT XP_024303660.1:n.*494_*495insATATATTGTAAATAT
NM_000141.5:c.*494_*495insATATATTGTAAATAT MANE Select NP_000132.3:n.*494_*495insATATATTGTAAATAT
NM_001144917.2:c.*494_*495insATATATTGTAAATAT NP_001138389.1:n.*494_*495insATATATTGTAAATAT
NM_001144918.2:c.*494_*495insATATATTGTAAATAT NP_001138390.1:n.*494_*495insATATATTGTAAATAT
NM_001320658.2:c.*494_*495insATATATTGTAAATAT NP_001307587.1:n.*494_*495insATATATTGTAAATAT
NR_073009.2:n.3396_3397insATATATTGTAAATAT
NM_001144915.2:c.*218_*219insATATATTGTAAATAT NP_001138387.1:n.*218_*219insATATATTGTAAATAT
NM_001144916.2:c.*494_*495insATATATTGTAAATAT NP_001138388.1:n.*494_*495insATATATTGTAAATAT
NM_001320654.2:c.*494_*495insATATATTGTAAATAT NP_001307583.1:n.*494_*495insATATATTGTAAATAT
Search 100 bp 5'
Search 100 bp 3'