Canonical Allele Identifier: CA1433506904

Gene: FGFR3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1804677_1804678delinsCT , CM000666.2:g.1804677_1804678delinsCT	GRCh38
NC_000004.11:g.1806404_1806405delinsCT , CM000666.1:g.1806404_1806405delinsCT	GRCh37
NC_000004.10:g.1776202_1776203delinsCT	NCBI36
NG_012632.1:g.16366_16367delinsCT , LRG_1021:g.16366_16367delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340107.9:c.1273-147_1273-146delinsCT	ENSP00000339824.4:n.1273-147_1273-146delinsCT
ENST00000260795.8:c.*323-147_*323-146delinsCT	ENSP00000260795.3:n.*323-147_*323-146delinsCT
ENST00000352904.6:c.931-147_931-146delinsCT	ENSP00000231803.1:n.931-147_931-146delinsCT
ENST00000412135.7:c.1255-147_1255-146delinsCT	ENSP00000412903.3:n.1255-147_1255-146delinsCT
ENST00000440486.8:c.1267-147_1267-146delinsCT MANE Select	ENSP00000414914.2:n.1267-147_1267-146delinsCT
ENST00000481110.7:c.1267-144_1267-143delinsCT	ENSP00000420533.2:n.1267-144_1267-143delinsCT
ENST00000260795.6:c.1267-147_1267-146delinsCT	ENSP00000260795.2:n.1267-147_1267-146delinsCT
ENST00000340107.8:c.1273-147_1273-146delinsCT	ENSP00000339824.4:n.1273-147_1273-146delinsCT
ENST00000352904.5:c.931-147_931-146delinsCT	ENSP00000231803.1:n.931-147_931-146delinsCT
ENST00000412135.6:c.931-147_931-146delinsCT	ENSP00000412903.2:n.931-147_931-146delinsCT
ENST00000440486.6:c.1267-147_1267-146delinsCT	ENSP00000414914.2:n.1267-147_1267-146delinsCT
ENST00000469068.1:n.186_187delinsCT
ENST00000481110.6:c.1267-144_1267-143delinsCT	ENSP00000420533.2:n.1267-144_1267-143delinsCT
ENST00000613647.4:c.*323-147_*323-146delinsCT	ENSP00000479472.1:n.*323-147_*323-146delinsCT
NM_000142.4:c.1267-147_1267-146delinsCT , LRG_1021t1:c.1267-147_1267-146delinsCT	NP_000133.1:n.1267-147_1267-146delinsCT
NM_001163213.1:c.1273-147_1273-146delinsCT , LRG_1021t2:c.1273-147_1273-146delinsCT	NP_001156685.1:n.1273-147_1273-146delinsCT
NM_022965.3:c.931-147_931-146delinsCT	NP_075254.1:n.931-147_931-146delinsCT
XM_006713868.1:c.1279-147_1279-146delinsCT	XP_006713931.1:n.1279-147_1279-146delinsCT
XM_006713869.1:c.1279-147_1279-146delinsCT	XP_006713932.1:n.1279-147_1279-146delinsCT
XM_006713870.1:c.1273-144_1273-143delinsCT	XP_006713933.1:n.1273-144_1273-143delinsCT
XM_006713871.1:c.1273-147_1273-146delinsCT	XP_006713934.1:n.1273-147_1273-146delinsCT
XM_006713872.1:c.1267-144_1267-143delinsCT	XP_006713935.1:n.1267-144_1267-143delinsCT
XM_006713873.1:c.1267-147_1267-146delinsCT	XP_006713936.1:n.1267-147_1267-146delinsCT
XM_011513420.1:c.1273-147_1273-146delinsCT	XP_011511722.1:n.1273-147_1273-146delinsCT
XM_011513422.1:c.1267-144_1267-143delinsCT	XP_011511724.1:n.1267-144_1267-143delinsCT
NM_001354809.1:c.1267-144_1267-143delinsCT	NP_001341738.1:n.1267-144_1267-143delinsCT
NM_001354810.1:c.1267-144_1267-143delinsCT	NP_001341739.1:n.1267-144_1267-143delinsCT
NR_148971.1:n.1674-147_1674-146delinsCT
NM_001354809.2:c.1267-144_1267-143delinsCT	NP_001341738.1:n.1267-144_1267-143delinsCT
NM_001354810.2:c.1267-144_1267-143delinsCT	NP_001341739.1:n.1267-144_1267-143delinsCT
NR_148971.2:n.1693-147_1693-146delinsCT
NM_000142.5:c.1267-147_1267-146delinsCT MANE Select	NP_000133.1:n.1267-147_1267-146delinsCT
NM_001163213.2:c.1273-147_1273-146delinsCT	NP_001156685.1:n.1273-147_1273-146delinsCT
NM_022965.4:c.931-147_931-146delinsCT	NP_075254.1:n.931-147_931-146delinsCT