Canonical Allele Identifier: CA1433507318
Gene: FGFR3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1805305_1805307delinsTGA , CM000666.2:g.1805305_1805307delinsTGA GRCh38
NC_000004.11:g.1807032_1807034delinsTGA , CM000666.1:g.1807032_1807034delinsTGA GRCh37
NC_000004.10:g.1776830_1776832delinsTGA NCBI36
NG_012632.1:g.16994_16996delinsTGA , LRG_1021:g.16994_16996delinsTGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000340107.9:c.1419-50_1419-48delinsTGA ENSP00000339824.4:n.1419-50_1419-48delinsTGA
ENST00000260795.8:c.*469-50_*469-48delinsTGA ENSP00000260795.3:n.*469-50_*469-48delinsTGA
ENST00000352904.6:c.1077-50_1077-48delinsTGA ENSP00000231803.1:n.1077-50_1077-48delinsTGA
ENST00000412135.7:c.1401-50_1401-48delinsTGA ENSP00000412903.3:n.1401-50_1401-48delinsTGA
ENST00000440486.8:c.1413-50_1413-48delinsTGA MANE Select ENSP00000414914.2:n.1413-50_1413-48delinsTGA
ENST00000481110.7:c.1416-50_1416-48delinsTGA ENSP00000420533.2:n.1416-50_1416-48delinsTGA
ENST00000260795.6:c.1413-50_1413-48delinsTGA ENSP00000260795.2:n.1413-50_1413-48delinsTGA
ENST00000340107.8:c.1419-50_1419-48delinsTGA ENSP00000339824.4:n.1419-50_1419-48delinsTGA
ENST00000352904.5:c.1077-50_1077-48delinsTGA ENSP00000231803.1:n.1077-50_1077-48delinsTGA
ENST00000412135.6:c.1077-50_1077-48delinsTGA ENSP00000412903.2:n.1077-50_1077-48delinsTGA
ENST00000440486.6:c.1413-50_1413-48delinsTGA ENSP00000414914.2:n.1413-50_1413-48delinsTGA
ENST00000469068.1:n.479-50_479-48delinsTGA
ENST00000481110.6:c.1416-50_1416-48delinsTGA ENSP00000420533.2:n.1416-50_1416-48delinsTGA
ENST00000613647.4:c.*469-50_*469-48delinsTGA ENSP00000479472.1:n.*469-50_*469-48delinsTGA
NM_000142.4:c.1413-50_1413-48delinsTGA , LRG_1021t1:c.1413-50_1413-48delinsTGA NP_000133.1:n.1413-50_1413-48delinsTGA
NM_001163213.1:c.1419-50_1419-48delinsTGA , LRG_1021t2:c.1419-50_1419-48delinsTGA NP_001156685.1:n.1419-50_1419-48delinsTGA
NM_022965.3:c.1077-50_1077-48delinsTGA NP_075254.1:n.1077-50_1077-48delinsTGA
XM_006713868.1:c.1425-50_1425-48delinsTGA XP_006713931.1:n.1425-50_1425-48delinsTGA
XM_006713869.1:c.1425-50_1425-48delinsTGA XP_006713932.1:n.1425-50_1425-48delinsTGA
XM_006713870.1:c.1422-50_1422-48delinsTGA XP_006713933.1:n.1422-50_1422-48delinsTGA
XM_006713871.1:c.1419-50_1419-48delinsTGA XP_006713934.1:n.1419-50_1419-48delinsTGA
XM_006713872.1:c.1416-50_1416-48delinsTGA XP_006713935.1:n.1416-50_1416-48delinsTGA
XM_006713873.1:c.1413-50_1413-48delinsTGA XP_006713936.1:n.1413-50_1413-48delinsTGA
XM_011513420.1:c.1419-50_1419-48delinsTGA XP_011511722.1:n.1419-50_1419-48delinsTGA
XM_011513422.1:c.1416-50_1416-48delinsTGA XP_011511724.1:n.1416-50_1416-48delinsTGA
NM_001354809.1:c.1416-50_1416-48delinsTGA NP_001341738.1:n.1416-50_1416-48delinsTGA
NM_001354810.1:c.1416-50_1416-48delinsTGA NP_001341739.1:n.1416-50_1416-48delinsTGA
NR_148971.1:n.1820-50_1820-48delinsTGA
NM_001354809.2:c.1416-50_1416-48delinsTGA NP_001341738.1:n.1416-50_1416-48delinsTGA
NM_001354810.2:c.1416-50_1416-48delinsTGA NP_001341739.1:n.1416-50_1416-48delinsTGA
NR_148971.2:n.1839-50_1839-48delinsTGA
NM_000142.5:c.1413-50_1413-48delinsTGA MANE Select NP_000133.1:n.1413-50_1413-48delinsTGA
NM_001163213.2:c.1419-50_1419-48delinsTGA NP_001156685.1:n.1419-50_1419-48delinsTGA
NM_022965.4:c.1077-50_1077-48delinsTGA NP_075254.1:n.1077-50_1077-48delinsTGA