Canonical Allele Identifier: CA2760148209

Gene: FGFR3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1805246_1805247insCC , CM000666.2:g.1805246_1805247insCC	GRCh38
NC_000004.11:g.1806973_1806974insCC , CM000666.1:g.1806973_1806974insCC	GRCh37
NC_000004.10:g.1776771_1776772insCC	NCBI36
NG_012632.1:g.16935_16936insCC , LRG_1021:g.16935_16936insCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340107.9:c.1419-109_1419-108insCC	ENSP00000339824.4:n.1419-109_1419-108insCC
ENST00000260795.8:c.*469-109_*469-108insCC	ENSP00000260795.3:n.*469-109_*469-108insCC
ENST00000352904.6:c.1077-109_1077-108insCC	ENSP00000231803.1:n.1077-109_1077-108insCC
ENST00000412135.7:c.1401-109_1401-108insCC	ENSP00000412903.3:n.1401-109_1401-108insCC
ENST00000440486.8:c.1413-109_1413-108insCC MANE Select	ENSP00000414914.2:n.1413-109_1413-108insCC
ENST00000481110.7:c.1416-109_1416-108insCC	ENSP00000420533.2:n.1416-109_1416-108insCC
ENST00000260795.6:c.1413-109_1413-108insCC	ENSP00000260795.2:n.1413-109_1413-108insCC
ENST00000340107.8:c.1419-109_1419-108insCC	ENSP00000339824.4:n.1419-109_1419-108insCC
ENST00000352904.5:c.1077-109_1077-108insCC	ENSP00000231803.1:n.1077-109_1077-108insCC
ENST00000412135.6:c.1077-109_1077-108insCC	ENSP00000412903.2:n.1077-109_1077-108insCC
ENST00000440486.6:c.1413-109_1413-108insCC	ENSP00000414914.2:n.1413-109_1413-108insCC
ENST00000469068.1:n.479-109_479-108insCC
ENST00000481110.6:c.1416-109_1416-108insCC	ENSP00000420533.2:n.1416-109_1416-108insCC
ENST00000613647.4:c.*469-109_*469-108insCC	ENSP00000479472.1:n.*469-109_*469-108insCC
NM_000142.4:c.1413-109_1413-108insCC , LRG_1021t1:c.1413-109_1413-108insCC	NP_000133.1:n.1413-109_1413-108insCC
NM_001163213.1:c.1419-109_1419-108insCC , LRG_1021t2:c.1419-109_1419-108insCC	NP_001156685.1:n.1419-109_1419-108insCC
NM_022965.3:c.1077-109_1077-108insCC	NP_075254.1:n.1077-109_1077-108insCC
XM_006713868.1:c.1425-109_1425-108insCC	XP_006713931.1:n.1425-109_1425-108insCC
XM_006713869.1:c.1425-109_1425-108insCC	XP_006713932.1:n.1425-109_1425-108insCC
XM_006713870.1:c.1422-109_1422-108insCC	XP_006713933.1:n.1422-109_1422-108insCC
XM_006713871.1:c.1419-109_1419-108insCC	XP_006713934.1:n.1419-109_1419-108insCC
XM_006713872.1:c.1416-109_1416-108insCC	XP_006713935.1:n.1416-109_1416-108insCC
XM_006713873.1:c.1413-109_1413-108insCC	XP_006713936.1:n.1413-109_1413-108insCC
XM_011513420.1:c.1419-109_1419-108insCC	XP_011511722.1:n.1419-109_1419-108insCC
XM_011513422.1:c.1416-109_1416-108insCC	XP_011511724.1:n.1416-109_1416-108insCC
NM_001354809.1:c.1416-109_1416-108insCC	NP_001341738.1:n.1416-109_1416-108insCC
NM_001354810.1:c.1416-109_1416-108insCC	NP_001341739.1:n.1416-109_1416-108insCC
NR_148971.1:n.1820-109_1820-108insCC
NM_001354809.2:c.1416-109_1416-108insCC	NP_001341738.1:n.1416-109_1416-108insCC
NM_001354810.2:c.1416-109_1416-108insCC	NP_001341739.1:n.1416-109_1416-108insCC
NR_148971.2:n.1839-109_1839-108insCC
NM_000142.5:c.1413-109_1413-108insCC MANE Select	NP_000133.1:n.1413-109_1413-108insCC
NM_001163213.2:c.1419-109_1419-108insCC	NP_001156685.1:n.1419-109_1419-108insCC
NM_022965.4:c.1077-109_1077-108insCC	NP_075254.1:n.1077-109_1077-108insCC