Canonical Allele Identifier: CA1433507330
Gene: FGFR3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1805326_1805327delinsAC , CM000666.2:g.1805326_1805327delinsAC GRCh38
NC_000004.11:g.1807053_1807054delinsAC , CM000666.1:g.1807053_1807054delinsAC GRCh37
NC_000004.10:g.1776851_1776852delinsAC NCBI36
NG_012632.1:g.17015_17016delinsAC , LRG_1021:g.17015_17016delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000340107.9:c.1419-29_1419-28delinsAC ENSP00000339824.4:n.1419-29_1419-28delinsAC
ENST00000260795.8:c.*469-29_*469-28delinsAC ENSP00000260795.3:n.*469-29_*469-28delinsAC
ENST00000352904.6:c.1077-29_1077-28delinsAC ENSP00000231803.1:n.1077-29_1077-28delinsAC
ENST00000412135.7:c.1401-29_1401-28delinsAC ENSP00000412903.3:n.1401-29_1401-28delinsAC
ENST00000440486.8:c.1413-29_1413-28delinsAC MANE Select ENSP00000414914.2:n.1413-29_1413-28delinsAC
ENST00000481110.7:c.1416-29_1416-28delinsAC ENSP00000420533.2:n.1416-29_1416-28delinsAC
ENST00000260795.6:c.1413-29_1413-28delinsAC ENSP00000260795.2:n.1413-29_1413-28delinsAC
ENST00000340107.8:c.1419-29_1419-28delinsAC ENSP00000339824.4:n.1419-29_1419-28delinsAC
ENST00000352904.5:c.1077-29_1077-28delinsAC ENSP00000231803.1:n.1077-29_1077-28delinsAC
ENST00000412135.6:c.1077-29_1077-28delinsAC ENSP00000412903.2:n.1077-29_1077-28delinsAC
ENST00000440486.6:c.1413-29_1413-28delinsAC ENSP00000414914.2:n.1413-29_1413-28delinsAC
ENST00000469068.1:n.479-29_479-28delinsAC
ENST00000481110.6:c.1416-29_1416-28delinsAC ENSP00000420533.2:n.1416-29_1416-28delinsAC
ENST00000613647.4:c.*469-29_*469-28delinsAC ENSP00000479472.1:n.*469-29_*469-28delinsAC
NM_000142.4:c.1413-29_1413-28delinsAC , LRG_1021t1:c.1413-29_1413-28delinsAC NP_000133.1:n.1413-29_1413-28delinsAC
NM_001163213.1:c.1419-29_1419-28delinsAC , LRG_1021t2:c.1419-29_1419-28delinsAC NP_001156685.1:n.1419-29_1419-28delinsAC
NM_022965.3:c.1077-29_1077-28delinsAC NP_075254.1:n.1077-29_1077-28delinsAC
XM_006713868.1:c.1425-29_1425-28delinsAC XP_006713931.1:n.1425-29_1425-28delinsAC
XM_006713869.1:c.1425-29_1425-28delinsAC XP_006713932.1:n.1425-29_1425-28delinsAC
XM_006713870.1:c.1422-29_1422-28delinsAC XP_006713933.1:n.1422-29_1422-28delinsAC
XM_006713871.1:c.1419-29_1419-28delinsAC XP_006713934.1:n.1419-29_1419-28delinsAC
XM_006713872.1:c.1416-29_1416-28delinsAC XP_006713935.1:n.1416-29_1416-28delinsAC
XM_006713873.1:c.1413-29_1413-28delinsAC XP_006713936.1:n.1413-29_1413-28delinsAC
XM_011513420.1:c.1419-29_1419-28delinsAC XP_011511722.1:n.1419-29_1419-28delinsAC
XM_011513422.1:c.1416-29_1416-28delinsAC XP_011511724.1:n.1416-29_1416-28delinsAC
NM_001354809.1:c.1416-29_1416-28delinsAC NP_001341738.1:n.1416-29_1416-28delinsAC
NM_001354810.1:c.1416-29_1416-28delinsAC NP_001341739.1:n.1416-29_1416-28delinsAC
NR_148971.1:n.1820-29_1820-28delinsAC
NM_001354809.2:c.1416-29_1416-28delinsAC NP_001341738.1:n.1416-29_1416-28delinsAC
NM_001354810.2:c.1416-29_1416-28delinsAC NP_001341739.1:n.1416-29_1416-28delinsAC
NR_148971.2:n.1839-29_1839-28delinsAC
NM_000142.5:c.1413-29_1413-28delinsAC MANE Select NP_000133.1:n.1413-29_1413-28delinsAC
NM_001163213.2:c.1419-29_1419-28delinsAC NP_001156685.1:n.1419-29_1419-28delinsAC
NM_022965.4:c.1077-29_1077-28delinsAC NP_075254.1:n.1077-29_1077-28delinsAC