Canonical Allele Identifier: CA1433505010

Gene: FGFR3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1801787_1801788delinsGT , CM000666.2:g.1801787_1801788delinsGT	GRCh38
NC_000004.11:g.1803514_1803515delinsGT , CM000666.1:g.1803514_1803515delinsGT	GRCh37
NC_000004.10:g.1773312_1773313delinsGT	NCBI36
NG_012632.1:g.13476_13477delinsGT , LRG_1021:g.13476_13477delinsGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000340107.9:c.739+44_739+45delinsGT	ENSP00000339824.4:n.739+44_739+45delinsGT...
ENST00000260795.8:c.739+44_739+45delinsGT	ENSP00000260795.3:n.739+44_739+45delinsGT...
ENST00000352904.6:c.739+44_739+45delinsGT	ENSP00000231803.1:n.739+44_739+45delinsGT...
ENST00000412135.7:c.727+44_727+45delinsGT	ENSP00000412903.3:n.727+44_727+45delinsGT...
ENST00000440486.8:c.739+44_739+45delinsGT MANE Select	ENSP00000414914.2:n.739+44_739+45delinsGT...
ENST00000481110.7:c.739+44_739+45delinsGT	ENSP00000420533.2:n.739+44_739+45delinsGT...
ENST00000260795.6:c.739+44_739+45delinsGT	ENSP00000260795.2:n.739+44_739+45delinsGT...
ENST00000340107.8:c.739+44_739+45delinsGT	ENSP00000339824.4:n.739+44_739+45delinsGT...
ENST00000352904.5:c.739+44_739+45delinsGT	ENSP00000231803.1:n.739+44_739+45delinsGT...
ENST00000412135.6:c.739+44_739+45delinsGT	ENSP00000412903.2:n.739+44_739+45delinsGT...
ENST00000440486.6:c.739+44_739+45delinsGT	ENSP00000414914.2:n.739+44_739+45delinsGT...
ENST00000474521.1:n.115+44_115+45delinsGT
ENST00000481110.6:c.739+44_739+45delinsGT	ENSP00000420533.2:n.739+44_739+45delinsGT...
ENST00000507588.1:c.199+44_199+45delinsGT	ENSP00000427289.1:n.199+44_199+45delinsGT...
ENST00000613647.4:c.739+44_739+45delinsGT	ENSP00000479472.1:n.739+44_739+45delinsGT...
NM_000142.4:c.739+44_739+45delinsGT , LRG_1021t1:c.739+44_739+45delinsGT	NP_000133.1:n.739+44_739+45delinsGT
NM_001163213.1:c.739+44_739+45delinsGT , LRG_1021t2:c.739+44_739+45delinsGT	NP_001156685.1:n.739+44_739+45delinsGT
NM_022965.3:c.739+44_739+45delinsGT	NP_075254.1:n.739+44_739+45delinsGT
XM_006713868.1:c.739+44_739+45delinsGT	XP_006713931.1:n.739+44_739+45delinsGT
XM_006713869.1:c.739+44_739+45delinsGT	XP_006713932.1:n.739+44_739+45delinsGT
XM_006713870.1:c.739+44_739+45delinsGT	XP_006713933.1:n.739+44_739+45delinsGT
XM_006713871.1:c.739+44_739+45delinsGT	XP_006713934.1:n.739+44_739+45delinsGT
XM_006713872.1:c.739+44_739+45delinsGT	XP_006713935.1:n.739+44_739+45delinsGT
XM_006713873.1:c.739+44_739+45delinsGT	XP_006713936.1:n.739+44_739+45delinsGT
XM_011513420.1:c.739+44_739+45delinsGT	XP_011511722.1:n.739+44_739+45delinsGT
XM_011513422.1:c.739+44_739+45delinsGT	XP_011511724.1:n.739+44_739+45delinsGT
NM_001354809.1:c.739+44_739+45delinsGT	NP_001341738.1:n.739+44_739+45delinsGT
NM_001354810.1:c.739+44_739+45delinsGT	NP_001341739.1:n.739+44_739+45delinsGT
NR_148971.1:n.995+44_995+45delinsGT
NM_001354809.2:c.739+44_739+45delinsGT	NP_001341738.1:n.739+44_739+45delinsGT
NM_001354810.2:c.739+44_739+45delinsGT	NP_001341739.1:n.739+44_739+45delinsGT
NR_148971.2:n.1014+44_1014+45delinsGT
NM_000142.5:c.739+44_739+45delinsGT MANE Select	NP_000133.1:n.739+44_739+45delinsGT
NM_001163213.2:c.739+44_739+45delinsGT	NP_001156685.1:n.739+44_739+45delinsGT
NM_022965.4:c.739+44_739+45delinsGT	NP_075254.1:n.739+44_739+45delinsGT