Canonical Allele Identifier: CA1941017729
Community Standard Title: NM_000141.5(FGFR2):c.1570A= (p.Thr524=)
Gene: FGFR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121498597T= , CM000672.2:g.121498597T= GRCh38
NC_000010.10:g.123258111T= , CM000672.1:g.123258111T= GRCh37
NC_000010.9:g.123248101T= NCBI36
NG_012449.1:g.104862A=
NG_012449.2:g.104862A=

Transcript Alleles

HGVS Amino-acid Change
NM_000141.5:c.1570A= MANE Select NP_000132.3:p.Thr524=
ENST00000358487.10:c.1570A= MANE Select ENSP00000351276.6:p.Thr524=
ENST00000457416.7:c.1573A= MANE Plus Clinical ENSP00000410294.2:p.Thr525=
NM_000141.4:c.1570A= NP_000132.3:p.Thr524=
NM_001144913.1:c.1573A= NP_001138385.1:p.Thr525=
NM_001144914.1:c.1234A= NP_001138386.1:p.Thr412=
NM_001144915.1:c.1303A= NP_001138387.1:p.Thr435=
NM_001144915.2:c.1303A= NP_001138387.1:p.Thr435=
NM_001144916.1:c.1225A= NP_001138388.1:p.Thr409=
NM_001144916.2:c.1225A= NP_001138388.1:p.Thr409=
NM_001144917.1:c.1222A= NP_001138389.1:p.Thr408=
NM_001144917.2:c.1222A= NP_001138389.1:p.Thr408=
NM_001144918.1:c.1219A= NP_001138390.1:p.Thr407=
NM_001144918.2:c.1219A= NP_001138390.1:p.Thr407=
NM_001144919.1:c.1306A= NP_001138391.1:p.Thr436=
NM_001144919.2:c.1306A= NP_001138391.1:p.Thr436=
NM_001320654.1:c.886A= NP_001307583.1:p.Thr296=
NM_001320654.2:c.886A= NP_001307583.1:p.Thr296=
NM_001320658.1:c.1564A= NP_001307587.1:p.Thr522=
NM_001320658.2:c.1564A= NP_001307587.1:p.Thr522=
NM_022970.3:c.1573A= NP_075259.4:p.Thr525=
NM_023029.2:c.1303A= NP_075418.1:p.Thr435=
NR_073009.1:n.2020A=
NR_073009.2:n.2006A=
ENST00000336553.10:c.1297A= ENSP00000337665.6:p.Thr433=
ENST00000346997.6:c.1564A= ENSP00000263451.5:p.Thr522=
ENST00000351936.10:c.1570A= ENSP00000309878.9:p.Thr524=
ENST00000351936.11:c.1564A= ENSP00000309878.10:p.Thr522=
ENST00000356226.8:c.1219A= ENSP00000348559.4:p.Thr407=
ENST00000357555.9:c.1303A= ENSP00000350166.5:p.Thr435=
ENST00000358487.9:c.1570A= ENSP00000351276.5:p.Thr524=
ENST00000360144.7:c.1306A= ENSP00000353262.3:p.Thr436=
ENST00000369056.5:c.1573A= ENSP00000358052.1:p.Thr525=
ENST00000369058.7:c.1573A= ENSP00000358054.3:p.Thr525=
ENST00000369059.5:c.1228A= ENSP00000358055.1:p.Thr410=
ENST00000369060.8:c.1222A= ENSP00000358056.4:p.Thr408=
ENST00000369061.8:c.1234A= ENSP00000358057.4:p.Thr412=
ENST00000429361.5:c.346A= ENSP00000404219.1:p.Thr116=
ENST00000457416.6:c.1573A= ENSP00000410294.2:p.Thr525=
ENST00000478859.5:c.886A= ENSP00000474011.1:p.Thr296=
ENST00000604236.5:c.*617A= ENSP00000474109.1:n.*617A=
ENST00000613048.4:c.1303A= ENSP00000484154.1:p.Thr435=
ENST00000638709.2:c.394A= ENSP00000491912.2:p.Thr132=
ENST00000682296.1:n.912A=
ENST00000682550.1:c.1219A= ENSP00000507633.1:p.Thr407=
ENST00000682772.1:c.394A= ENSP00000506848.1:p.Thr132=
ENST00000682904.1:n.390A=
ENST00000683211.1:c.1564A= ENSP00000508257.1:p.Thr522=
ENST00000683250.1:c.*272A= ENSP00000506847.1:n.*272A=
ENST00000683418.1:n.3911A=
ENST00000684153.1:c.1219A= ENSP00000506937.1:p.Thr407=
ENST00000684516.1:n.2583A=
XM_006717708.2:c.1624A= XP_006717771.1:p.Thr542=
XM_006717708.3:c.1624A= XP_006717771.1:p.Thr542=
XM_006717709.2:c.1621A= XP_006717772.1:p.Thr541=
XM_006717710.2:c.1630A= XP_006717773.1:p.Thr544=
XM_006717710.4:c.1630A= XP_006717773.1:p.Thr544=
XM_006717711.2:c.1363A= XP_006717774.1:p.Thr455=
XM_006717712.2:c.1285A= XP_006717775.1:p.Thr429=
XM_006717713.2:c.1627A= XP_006717776.1:p.Thr543=
XM_011539510.1:c.886A= XP_011537812.1:p.Thr296=
XM_017015920.2:c.1624A= XP_016871409.1:p.Thr542=
XM_017015921.2:c.1621A= XP_016871410.1:p.Thr541=
XM_017015924.2:c.1282A= XP_016871413.1:p.Thr428=
XM_017015925.2:c.1276A= XP_016871414.1:p.Thr426=
XM_024447887.1:c.1360A= XP_024303655.1:p.Thr454=
XM_024447888.1:c.1357A= XP_024303656.1:p.Thr453=
XM_024447889.1:c.1354A= XP_024303657.1:p.Thr452=
XM_024447890.1:c.1363A= XP_024303658.1:p.Thr455=
XM_024447891.1:c.1285A= XP_024303659.1:p.Thr429=
XM_024447892.1:c.400A= XP_024303660.1:p.Thr134=