Canonical Allele Identifier: CA5720447
Community Standard Title: NM_000141.5(FGFR2):c.2426T>C (p.Leu809Pro)
Gene: FGFR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121479897A>G , CM000672.2:g.121479897A>G GRCh38
NC_000010.10:g.123239411A>G , CM000672.1:g.123239411A>G GRCh37
NC_000010.9:g.123229401A>G NCBI36
NG_012449.1:g.123562T>C
NG_012449.2:g.123562T>C

Transcript Alleles

HGVS Amino-acid Change
NM_000141.5:c.2426T>C MANE Select NP_000132.3:p.Leu809Pro
ENST00000358487.10:c.2426T>C MANE Select ENSP00000351276.6:p.Leu809Pro
ENST00000457416.7:c.2429T>C MANE Plus Clinical ENSP00000410294.2:p.Leu810Pro
NM_000141.4:c.2426T>C NP_000132.3:p.Leu809Pro
NM_001144914.1:c.2090T>C NP_001138386.1:p.Leu697Pro
NM_001144915.1:c.2035-227T>C NP_001138387.1:n.2035-227T>C
NM_001144915.2:c.2035-227T>C NP_001138387.1:n.2035-227T>C
NM_001144916.1:c.2081T>C NP_001138388.1:p.Leu694Pro
NM_001144916.2:c.2081T>C NP_001138388.1:p.Leu694Pro
NM_001144917.1:c.2078T>C NP_001138389.1:p.Leu693Pro
NM_001144917.2:c.2078T>C NP_001138389.1:p.Leu693Pro
NM_001144918.1:c.2075T>C NP_001138390.1:p.Leu692Pro
NM_001144918.2:c.2075T>C NP_001138390.1:p.Leu692Pro
NM_001320654.1:c.1742T>C NP_001307583.1:p.Leu581Pro
NM_001320654.2:c.1742T>C NP_001307583.1:p.Leu581Pro
NM_001320658.1:c.2420T>C NP_001307587.1:p.Leu807Pro
NM_001320658.2:c.2420T>C NP_001307587.1:p.Leu807Pro
NM_022970.3:c.2429T>C NP_075259.4:p.Leu810Pro
NM_023029.2:c.2159T>C NP_075418.1:p.Leu720Pro
NR_073009.1:n.2876T>C
NR_073009.2:n.2862T>C
ENST00000346997.6:c.2420T>C ENSP00000263451.5:p.Leu807Pro
ENST00000351936.10:c.2426T>C ENSP00000309878.9:p.Leu809Pro
ENST00000351936.11:c.2420T>C ENSP00000309878.10:p.Leu807Pro
ENST00000356226.8:c.2075T>C ENSP00000348559.4:p.Leu692Pro
ENST00000357555.9:c.2035-227T>C ENSP00000350166.5:n.2035-227T>C
ENST00000358487.9:c.2426T>C ENSP00000351276.5:p.Leu809Pro
ENST00000369059.5:c.2084T>C ENSP00000358055.1:p.Leu695Pro
ENST00000369060.8:c.2078T>C ENSP00000358056.4:p.Leu693Pro
ENST00000369061.8:c.2090T>C ENSP00000358057.4:p.Leu697Pro
ENST00000429361.5:c.1096T>C ENSP00000404219.1:p.Phe366Leu
ENST00000457416.6:c.2429T>C ENSP00000410294.2:p.Leu810Pro
ENST00000467584.1:n.385T>C
ENST00000478859.5:c.1742T>C ENSP00000474011.1:p.Leu581Pro
ENST00000604236.5:c.*1473T>C ENSP00000474109.1:n.*1473T>C
ENST00000613048.4:c.2159T>C ENSP00000484154.1:p.Leu720Pro
ENST00000638709.1:c.413T>C
ENST00000638709.2:c.1250T>C ENSP00000491912.2:p.Leu417Pro
ENST00000682296.1:n.1768T>C
ENST00000682550.1:c.2075T>C ENSP00000507633.1:p.Leu692Pro
ENST00000682772.1:c.1250T>C ENSP00000506848.1:p.Leu417Pro
ENST00000682904.1:n.1246T>C
ENST00000683029.1:n.2429T>C
ENST00000683211.1:c.2420T>C ENSP00000508257.1:p.Leu807Pro
ENST00000683250.1:c.*2719T>C ENSP00000506847.1:n.*2719T>C
ENST00000683418.1:n.4767T>C
ENST00000684153.1:c.*154T>C ENSP00000506937.1:n.*154T>C
ENST00000684516.1:n.3439T>C
XM_006717708.2:c.2480T>C XP_006717771.1:p.Leu827Pro
XM_006717708.3:c.2480T>C XP_006717771.1:p.Leu827Pro
XM_006717709.2:c.2477T>C XP_006717772.1:p.Leu826Pro
XM_006717710.2:c.*154T>C XP_006717773.1:n.*154T>C
XM_006717710.4:c.*154T>C XP_006717773.1:n.*154T>C
XM_006717711.2:c.2219T>C XP_006717774.1:p.Leu740Pro
XM_006717712.2:c.2141T>C XP_006717775.1:p.Leu714Pro
XM_006717713.2:c.*154T>C XP_006717776.1:n.*154T>C
XM_011539510.1:c.1742T>C XP_011537812.1:p.Leu581Pro
XM_017015920.2:c.*154T>C XP_016871409.1:n.*154T>C
XM_017015921.2:c.*154T>C XP_016871410.1:n.*154T>C
XM_017015924.2:c.2138T>C XP_016871413.1:p.Leu713Pro
XM_017015925.2:c.*154T>C XP_016871414.1:n.*154T>C
XM_024447887.1:c.2216T>C XP_024303655.1:p.Leu739Pro
XM_024447888.1:c.2213T>C XP_024303656.1:p.Leu738Pro
XM_024447889.1:c.2210T>C XP_024303657.1:p.Leu737Pro
XM_024447890.1:c.2219T>C XP_024303658.1:p.Leu740Pro
XM_024447891.1:c.2141T>C XP_024303659.1:p.Leu714Pro
XM_024447892.1:c.1256T>C XP_024303660.1:p.Leu419Pro