Canonical Allele Identifier: CA1433507425

Gene: FGFR3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1805491_1805492delinsGC , CM000666.2:g.1805491_1805492delinsGC	GRCh38
NC_000004.11:g.1807218_1807219delinsGC , CM000666.1:g.1807218_1807219delinsGC	GRCh37
NC_000004.10:g.1777016_1777017delinsGC	NCBI36
NG_012632.1:g.17180_17181delinsGC , LRG_1021:g.17180_17181delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340107.9:c.1540+15_1540+16delinsGC	ENSP00000339824.4:n.1540+15_1540+16delinsGC
ENST00000260795.8:c.*590+15_*590+16delinsGC	ENSP00000260795.3:n.*590+15_*590+16delinsGC
ENST00000352904.6:c.1198+15_1198+16delinsGC	ENSP00000231803.1:n.1198+15_1198+16delinsGC
ENST00000412135.7:c.1522+15_1522+16delinsGC	ENSP00000412903.3:n.1522+15_1522+16delinsGC
ENST00000440486.8:c.1534+15_1534+16delinsGC MANE Select	ENSP00000414914.2:n.1534+15_1534+16delinsGC
ENST00000481110.7:c.1537+15_1537+16delinsGC	ENSP00000420533.2:n.1537+15_1537+16delinsGC
ENST00000260795.6:c.1534+15_1534+16delinsGC	ENSP00000260795.2:n.1534+15_1534+16delinsGC
ENST00000340107.8:c.1540+15_1540+16delinsGC	ENSP00000339824.4:n.1540+15_1540+16delinsGC
ENST00000352904.5:c.1198+15_1198+16delinsGC	ENSP00000231803.1:n.1198+15_1198+16delinsGC
ENST00000412135.6:c.1198+15_1198+16delinsGC	ENSP00000412903.2:n.1198+15_1198+16delinsGC
ENST00000440486.6:c.1534+15_1534+16delinsGC	ENSP00000414914.2:n.1534+15_1534+16delinsGC
ENST00000469068.1:n.600+15_600+16delinsGC
ENST00000481110.6:c.1537+15_1537+16delinsGC	ENSP00000420533.2:n.1537+15_1537+16delinsGC
ENST00000613647.4:c.*590+15_*590+16delinsGC	ENSP00000479472.1:n.*590+15_*590+16delinsGC
NM_000142.4:c.1534+15_1534+16delinsGC , LRG_1021t1:c.1534+15_1534+16delinsGC	NP_000133.1:n.1534+15_1534+16delinsGC
NM_001163213.1:c.1540+15_1540+16delinsGC , LRG_1021t2:c.1540+15_1540+16delinsGC	NP_001156685.1:n.1540+15_1540+16delinsGC
NM_022965.3:c.1198+15_1198+16delinsGC	NP_075254.1:n.1198+15_1198+16delinsGC
XM_006713868.1:c.1546+15_1546+16delinsGC	XP_006713931.1:n.1546+15_1546+16delinsGC
XM_006713869.1:c.1546+15_1546+16delinsGC	XP_006713932.1:n.1546+15_1546+16delinsGC
XM_006713870.1:c.1543+15_1543+16delinsGC	XP_006713933.1:n.1543+15_1543+16delinsGC
XM_006713871.1:c.1540+15_1540+16delinsGC	XP_006713934.1:n.1540+15_1540+16delinsGC
XM_006713872.1:c.1537+15_1537+16delinsGC	XP_006713935.1:n.1537+15_1537+16delinsGC
XM_006713873.1:c.1534+15_1534+16delinsGC	XP_006713936.1:n.1534+15_1534+16delinsGC
XM_011513420.1:c.1540+15_1540+16delinsGC	XP_011511722.1:n.1540+15_1540+16delinsGC
XM_011513422.1:c.1537+15_1537+16delinsGC	XP_011511724.1:n.1537+15_1537+16delinsGC
NM_001354809.1:c.1537+15_1537+16delinsGC	NP_001341738.1:n.1537+15_1537+16delinsGC
NM_001354810.1:c.1537+15_1537+16delinsGC	NP_001341739.1:n.1537+15_1537+16delinsGC
NR_148971.1:n.1941+15_1941+16delinsGC
NM_001354809.2:c.1537+15_1537+16delinsGC	NP_001341738.1:n.1537+15_1537+16delinsGC
NM_001354810.2:c.1537+15_1537+16delinsGC	NP_001341739.1:n.1537+15_1537+16delinsGC
NR_148971.2:n.1960+15_1960+16delinsGC
NM_000142.5:c.1534+15_1534+16delinsGC MANE Select	NP_000133.1:n.1534+15_1534+16delinsGC
NM_001163213.2:c.1540+15_1540+16delinsGC	NP_001156685.1:n.1540+15_1540+16delinsGC
NM_022965.4:c.1198+15_1198+16delinsGC	NP_075254.1:n.1198+15_1198+16delinsGC