Canonical Allele Identifier: CA645526887
Gene: FGFR3 HGNC NCBI

Linked Data

COSMIC: COSM86030

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1801838_1801843del , CM000666.2:g.1801838_1801843del GRCh38
NC_000004.11:g.1803565_1803570del , CM000666.1:g.1803565_1803570del GRCh37
NC_000004.10:g.1773363_1773368del NCBI36
NG_012632.1:g.13527_13532del , LRG_1021:g.13527_13532del

Transcript Alleles

HGVS Amino-acid change
ENST00000340107.9:c.743_748del ENSP00000339824.4:p.Arg248_Ser249del
ENST00000260795.8:c.743_748del ENSP00000260795.3:p.Arg248_Ser249del
ENST00000352904.6:c.743_748del ENSP00000231803.1:p.Arg248_Ser249del
ENST00000412135.7:c.731_736del ENSP00000412903.3:p.Arg244_Ser245del
ENST00000440486.8:c.743_748del MANE Select ENSP00000414914.2:p.Arg248_Ser249del
ENST00000481110.7:c.743_748del ENSP00000420533.2:p.Arg248_Ser249del
ENST00000260795.6:c.743_748del ENSP00000260795.2:p.Arg248_Ser249del
ENST00000340107.8:c.743_748del ENSP00000339824.4:p.Arg248_Ser249del
ENST00000352904.5:c.743_748del ENSP00000231803.1:p.Arg248_Ser249del
ENST00000412135.6:c.743_748del ENSP00000412903.2:p.Arg248_Ser249del
ENST00000440486.6:c.743_748del ENSP00000414914.2:p.Arg248_Ser249del
ENST00000474521.1:n.119_124del
ENST00000481110.6:c.743_748del ENSP00000420533.2:p.Arg248_Ser249del
ENST00000507588.1:c.203_208del ENSP00000427289.1:p.Arg68_Ser69del
ENST00000613647.4:c.743_748del ENSP00000479472.1:p.Arg248_Ser249del
NM_000142.4:c.743_748del , LRG_1021t1:c.743_748del NP_000133.1:p.Arg248_Ser249del
NM_001163213.1:c.743_748del , LRG_1021t2:c.743_748del NP_001156685.1:p.Arg248_Ser249del
NM_022965.3:c.743_748del NP_075254.1:p.Arg248_Ser249del
XM_006713868.1:c.743_748del XP_006713931.1:p.Arg248_Ser249del
XM_006713869.1:c.743_748del XP_006713932.1:p.Arg248_Ser249del
XM_006713870.1:c.743_748del XP_006713933.1:p.Arg248_Ser249del
XM_006713871.1:c.743_748del XP_006713934.1:p.Arg248_Ser249del
XM_006713872.1:c.743_748del XP_006713935.1:p.Arg248_Ser249del
XM_006713873.1:c.743_748del XP_006713936.1:p.Arg248_Ser249del
XM_011513420.1:c.743_748del XP_011511722.1:p.Arg248_Ser249del
XM_011513422.1:c.743_748del XP_011511724.1:p.Arg248_Ser249del
NM_001354809.1:c.743_748del NP_001341738.1:p.Arg248_Ser249del
NM_001354810.1:c.743_748del NP_001341739.1:p.Arg248_Ser249del
NR_148971.1:n.999_1004del
NM_001354809.2:c.743_748del NP_001341738.1:p.Arg248_Ser249del
NM_001354810.2:c.743_748del NP_001341739.1:p.Arg248_Ser249del
NR_148971.2:n.1018_1023del
NM_000142.5:c.743_748del MANE Select NP_000133.1:p.Arg248_Ser249del
NM_001163213.2:c.743_748del NP_001156685.1:p.Arg248_Ser249del
NM_022965.4:c.743_748del NP_075254.1:p.Arg248_Ser249del