Canonical Allele Identifier: CA1433507448

Gene: FGFR3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1805517_1805520delinsGCGC , CM000666.2:g.1805517_1805520delinsGCGC	GRCh38
NC_000004.11:g.1807244_1807247delinsGCGC , CM000666.1:g.1807244_1807247delinsGCGC	GRCh37
NC_000004.10:g.1777042_1777045delinsGCGC	NCBI36
NG_012632.1:g.17206_17209delinsGCGC , LRG_1021:g.17206_17209delinsGCGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340107.9:c.1541-42_1541-39delinsGCGC	ENSP00000339824.4:n.1541-42_1541-39delinsGCGC
ENST00000260795.8:c.*591-42_*591-39delinsGCGC	ENSP00000260795.3:n.*591-42_*591-39delinsGCGC
ENST00000352904.6:c.1199-42_1199-39delinsGCGC	ENSP00000231803.1:n.1199-42_1199-39delinsGCGC
ENST00000412135.7:c.1523-42_1523-39delinsGCGC	ENSP00000412903.3:n.1523-42_1523-39delinsGCGC
ENST00000440486.8:c.1535-42_1535-39delinsGCGC MANE Select	ENSP00000414914.2:n.1535-42_1535-39delinsGCGC
ENST00000481110.7:c.1538-42_1538-39delinsGCGC	ENSP00000420533.2:n.1538-42_1538-39delinsGCGC
ENST00000260795.6:c.1535-42_1535-39delinsGCGC	ENSP00000260795.2:n.1535-42_1535-39delinsGCGC
ENST00000340107.8:c.1541-42_1541-39delinsGCGC	ENSP00000339824.4:n.1541-42_1541-39delinsGCGC
ENST00000352904.5:c.1199-42_1199-39delinsGCGC	ENSP00000231803.1:n.1199-42_1199-39delinsGCGC
ENST00000412135.6:c.1199-42_1199-39delinsGCGC	ENSP00000412903.2:n.1199-42_1199-39delinsGCGC
ENST00000440486.6:c.1535-42_1535-39delinsGCGC	ENSP00000414914.2:n.1535-42_1535-39delinsGCGC
ENST00000469068.1:n.601-42_601-39delinsGCGC
ENST00000481110.6:c.1538-42_1538-39delinsGCGC	ENSP00000420533.2:n.1538-42_1538-39delinsGCGC
ENST00000613647.4:c.*591-42_*591-39delinsGCGC	ENSP00000479472.1:n.*591-42_*591-39delinsGCGC
NM_000142.4:c.1535-42_1535-39delinsGCGC , LRG_1021t1:c.1535-42_1535-39delinsGCGC	NP_000133.1:n.1535-42_1535-39delinsGCGC
NM_001163213.1:c.1541-42_1541-39delinsGCGC , LRG_1021t2:c.1541-42_1541-39delinsGCGC	NP_001156685.1:n.1541-42_1541-39delinsGCGC
NM_022965.3:c.1199-42_1199-39delinsGCGC	NP_075254.1:n.1199-42_1199-39delinsGCGC
XM_006713868.1:c.1547-42_1547-39delinsGCGC	XP_006713931.1:n.1547-42_1547-39delinsGCGC
XM_006713869.1:c.1547-42_1547-39delinsGCGC	XP_006713932.1:n.1547-42_1547-39delinsGCGC
XM_006713870.1:c.1544-42_1544-39delinsGCGC	XP_006713933.1:n.1544-42_1544-39delinsGCGC
XM_006713871.1:c.1541-42_1541-39delinsGCGC	XP_006713934.1:n.1541-42_1541-39delinsGCGC
XM_006713872.1:c.1538-42_1538-39delinsGCGC	XP_006713935.1:n.1538-42_1538-39delinsGCGC
XM_006713873.1:c.1535-42_1535-39delinsGCGC	XP_006713936.1:n.1535-42_1535-39delinsGCGC
XM_011513420.1:c.1541-42_1541-39delinsGCGC	XP_011511722.1:n.1541-42_1541-39delinsGCGC
XM_011513422.1:c.1538-42_1538-39delinsGCGC	XP_011511724.1:n.1538-42_1538-39delinsGCGC
NM_001354809.1:c.1538-42_1538-39delinsGCGC	NP_001341738.1:n.1538-42_1538-39delinsGCGC
NM_001354810.1:c.1538-42_1538-39delinsGCGC	NP_001341739.1:n.1538-42_1538-39delinsGCGC
NR_148971.1:n.1942-42_1942-39delinsGCGC
NM_001354809.2:c.1538-42_1538-39delinsGCGC	NP_001341738.1:n.1538-42_1538-39delinsGCGC
NM_001354810.2:c.1538-42_1538-39delinsGCGC	NP_001341739.1:n.1538-42_1538-39delinsGCGC
NR_148971.2:n.1961-42_1961-39delinsGCGC
NM_000142.5:c.1535-42_1535-39delinsGCGC MANE Select	NP_000133.1:n.1535-42_1535-39delinsGCGC
NM_001163213.2:c.1541-42_1541-39delinsGCGC	NP_001156685.1:n.1541-42_1541-39delinsGCGC
NM_022965.4:c.1199-42_1199-39delinsGCGC	NP_075254.1:n.1199-42_1199-39delinsGCGC