Canonical Allele Identifier: CA2563626920
Gene: FGFR3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1805964_1805970del , CM000666.2:g.1805964_1805970del GRCh38
NC_000004.11:g.1807691_1807697del , CM000666.1:g.1807691_1807697del GRCh37
NC_000004.10:g.1777489_1777495del NCBI36
NG_012632.1:g.17653_17659del , LRG_1021:g.17653_17659del

Transcript Alleles

HGVS Amino-acid Change
ENST00000340107.9:c.1842+24_1842+30del ENSP00000339824.4:n.1842+24_1842+30del
ENST00000260795.8:c.*892+24_*892+30del ENSP00000260795.3:n.*892+24_*892+30del
ENST00000352904.6:c.1500+24_1500+30del ENSP00000231803.1:n.1500+24_1500+30del
ENST00000412135.7:c.1824+24_1824+30del ENSP00000412903.3:n.1824+24_1824+30del
ENST00000440486.8:c.1836+24_1836+30del MANE Select ENSP00000414914.2:n.1836+24_1836+30del
ENST00000481110.7:c.1839+24_1839+30del ENSP00000420533.2:n.1839+24_1839+30del
ENST00000260795.6:c.1836+24_1836+30del ENSP00000260795.2:n.1836+24_1836+30del
ENST00000340107.8:c.1842+24_1842+30del ENSP00000339824.4:n.1842+24_1842+30del
ENST00000352904.5:c.1500+24_1500+30del ENSP00000231803.1:n.1500+24_1500+30del
ENST00000412135.6:c.1500+24_1500+30del ENSP00000412903.2:n.1500+24_1500+30del
ENST00000440486.6:c.1836+24_1836+30del ENSP00000414914.2:n.1836+24_1836+30del
ENST00000481110.6:c.1839+24_1839+30del ENSP00000420533.2:n.1839+24_1839+30del
ENST00000613647.4:c.*892+24_*892+30del ENSP00000479472.1:n.*892+24_*892+30del
NM_000142.4:c.1836+24_1836+30del , LRG_1021t1:c.1836+24_1836+30del NP_000133.1:n.1836+24_1836+30del
NM_001163213.1:c.1842+24_1842+30del , LRG_1021t2:c.1842+24_1842+30del NP_001156685.1:n.1842+24_1842+30del
NM_022965.3:c.1500+24_1500+30del NP_075254.1:n.1500+24_1500+30del
XM_006713868.1:c.1848+24_1848+30del XP_006713931.1:n.1848+24_1848+30del
XM_006713869.1:c.1848+24_1848+30del XP_006713932.1:n.1848+24_1848+30del
XM_006713870.1:c.1845+24_1845+30del XP_006713933.1:n.1845+24_1845+30del
XM_006713871.1:c.1842+24_1842+30del XP_006713934.1:n.1842+24_1842+30del
XM_006713872.1:c.1839+24_1839+30del XP_006713935.1:n.1839+24_1839+30del
XM_006713873.1:c.1836+24_1836+30del XP_006713936.1:n.1836+24_1836+30del
XM_011513420.1:c.1842+24_1842+30del XP_011511722.1:n.1842+24_1842+30del
XM_011513422.1:c.1839+24_1839+30del XP_011511724.1:n.1839+24_1839+30del
NM_001354809.1:c.1839+24_1839+30del NP_001341738.1:n.1839+24_1839+30del
NM_001354810.1:c.1839+24_1839+30del NP_001341739.1:n.1839+24_1839+30del
NR_148971.1:n.2243+24_2243+30del
NM_001354809.2:c.1839+24_1839+30del NP_001341738.1:n.1839+24_1839+30del
NM_001354810.2:c.1839+24_1839+30del NP_001341739.1:n.1839+24_1839+30del
NR_148971.2:n.2262+24_2262+30del
NM_000142.5:c.1836+24_1836+30del MANE Select NP_000133.1:n.1836+24_1836+30del
NM_001163213.2:c.1842+24_1842+30del NP_001156685.1:n.1842+24_1842+30del
NM_022965.4:c.1500+24_1500+30del NP_075254.1:n.1500+24_1500+30del