Canonical Allele Identifier: CA378314308

Gene: FGFR2

Linked Data

• dbSNP Id: rs2133835339
• MyVariant Identifiers: chr10:g.123247527T>A (hg19) ; chr10:g.121488013T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121488013T>A , CM000672.2:g.121488013T>A	GRCh38
NC_000010.10:g.123247527T>A , CM000672.1:g.123247527T>A	GRCh37
NC_000010.9:g.123237517T>A	NCBI36
NG_012449.1:g.115446A>T
NG_012449.2:g.115446A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000457416.7:c.1967A>T MANE Plus Clinical	ENSP00000410294.2:p.Asp656Val
ENST00000351936.11:c.1958A>T	ENSP00000309878.10:p.Asp653Val
ENST00000638709.2:c.788A>T	ENSP00000491912.2:p.Asp263Val
ENST00000682296.1:n.1306A>T
ENST00000682550.1:c.1613A>T	ENSP00000507633.1:p.Asp538Val
ENST00000682772.1:c.788A>T	ENSP00000506848.1:p.Asp263Val
ENST00000682904.1:n.784A>T
ENST00000683029.1:n.376A>T
ENST00000683211.1:c.1958A>T	ENSP00000508257.1:p.Asp653Val
ENST00000683250.1:c.*666A>T	ENSP00000506847.1:n.*666A>T
ENST00000683418.1:n.4305A>T
ENST00000684153.1:c.1613A>T	ENSP00000506937.1:p.Asp538Val
ENST00000684516.1:n.2977A>T
ENST00000358487.10:c.1964A>T MANE Select	ENSP00000351276.6:p.Asp655Val
ENST00000336553.10:c.1691A>T	ENSP00000337665.6:p.Asp564Val
ENST00000346997.6:c.1958A>T	ENSP00000263451.5:p.Asp653Val
ENST00000351936.10:c.1964A>T	ENSP00000309878.9:p.Asp655Val
ENST00000356226.8:c.1613A>T	ENSP00000348559.4:p.Asp538Val
ENST00000357555.9:c.1697A>T	ENSP00000350166.5:p.Asp566Val
ENST00000358487.9:c.1964A>T	ENSP00000351276.5:p.Asp655Val
ENST00000360144.7:c.1700A>T	ENSP00000353262.3:p.Asp567Val
ENST00000369056.5:c.1967A>T	ENSP00000358052.1:p.Asp656Val
ENST00000369058.7:c.1967A>T	ENSP00000358054.3:p.Asp656Val
ENST00000369059.5:c.1622A>T	ENSP00000358055.1:p.Asp541Val
ENST00000369060.8:c.1616A>T	ENSP00000358056.4:p.Asp539Val
ENST00000369061.8:c.1628A>T	ENSP00000358057.4:p.Asp543Val
ENST00000429361.5:c.740A>T	ENSP00000404219.1:p.Asp247Val
ENST00000457416.6:c.1967A>T	ENSP00000410294.2:p.Asp656Val
ENST00000478859.5:c.1280A>T	ENSP00000474011.1:p.Asp427Val
ENST00000604236.5:c.*1011A>T	ENSP00000474109.1:n.*1011A>T
ENST00000613048.4:c.1697A>T	ENSP00000484154.1:p.Asp566Val
NM_000141.4:c.1964A>T	NP_000132.3:p.Asp655Val
NM_001144913.1:c.1967A>T	NP_001138385.1:p.Asp656Val
NM_001144914.1:c.1628A>T	NP_001138386.1:p.Asp543Val
NM_001144915.1:c.1697A>T	NP_001138387.1:p.Asp566Val
NM_001144916.1:c.1619A>T	NP_001138388.1:p.Asp540Val
NM_001144917.1:c.1616A>T	NP_001138389.1:p.Asp539Val
NM_001144918.1:c.1613A>T	NP_001138390.1:p.Asp538Val
NM_001144919.1:c.1700A>T	NP_001138391.1:p.Asp567Val
NM_022970.3:c.1967A>T	NP_075259.4:p.Asp656Val
NM_023029.2:c.1697A>T	NP_075418.1:p.Asp566Val
NR_073009.1:n.2414A>T
XM_006717708.2:c.2018A>T	XP_006717771.1:p.Asp673Val
XM_006717709.2:c.2015A>T	XP_006717772.1:p.Asp672Val
XM_006717710.2:c.2024A>T	XP_006717773.1:p.Asp675Val
XM_006717711.2:c.1757A>T	XP_006717774.1:p.Asp586Val
XM_006717712.2:c.1679A>T	XP_006717775.1:p.Asp560Val
XM_006717713.2:c.2021A>T	XP_006717776.1:p.Asp674Val
XM_011539510.1:c.1280A>T	XP_011537812.1:p.Asp427Val
NM_001320654.1:c.1280A>T	NP_001307583.1:p.Asp427Val
NM_001320658.1:c.1958A>T	NP_001307587.1:p.Asp653Val
XM_006717708.3:c.2018A>T	XP_006717771.1:p.Asp673Val
XM_006717710.4:c.2024A>T	XP_006717773.1:p.Asp675Val
XM_017015920.2:c.2018A>T	XP_016871409.1:p.Asp673Val
XM_017015921.2:c.2015A>T	XP_016871410.1:p.Asp672Val
XM_017015924.2:c.1676A>T	XP_016871413.1:p.Asp559Val
XM_017015925.2:c.1670A>T	XP_016871414.1:p.Asp557Val
XM_024447887.1:c.1754A>T	XP_024303655.1:p.Asp585Val
XM_024447888.1:c.1751A>T	XP_024303656.1:p.Asp584Val
XM_024447889.1:c.1748A>T	XP_024303657.1:p.Asp583Val
XM_024447890.1:c.1757A>T	XP_024303658.1:p.Asp586Val
XM_024447891.1:c.1679A>T	XP_024303659.1:p.Asp560Val
XM_024447892.1:c.794A>T	XP_024303660.1:p.Asp265Val
NM_000141.5:c.1964A>T MANE Select	NP_000132.3:p.Asp655Val
NM_001144917.2:c.1616A>T	NP_001138389.1:p.Asp539Val
NM_001144918.2:c.1613A>T	NP_001138390.1:p.Asp538Val
NM_001144919.2:c.1700A>T	NP_001138391.1:p.Asp567Val
NM_001320658.2:c.1958A>T	NP_001307587.1:p.Asp653Val
NR_073009.2:n.2400A>T
NM_001144915.2:c.1697A>T	NP_001138387.1:p.Asp566Val
NM_001144916.2:c.1619A>T	NP_001138388.1:p.Asp540Val
NM_001320654.2:c.1280A>T	NP_001307583.1:p.Asp427Val