Canonical Allele Identifier: CA1433506899

Gene: FGFR3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1804671_1804680delinsAGGGTACTTT , CM000666.2:g.1804671_1804680delinsAGGGTACTTT	GRCh38
NC_000004.11:g.1806398_1806407delinsAGGGTACTTT , CM000666.1:g.1806398_1806407delinsAGGGTACTTT	GRCh37
NC_000004.10:g.1776196_1776205delinsAGGGTACTTT	NCBI36
NG_012632.1:g.16360_16369delinsAGGGTACTTT , LRG_1021:g.16360_16369delinsAGGGTACTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340107.9:c.1272+151_1273-144delinsAGGGTACTTT	ENSP00000339824.4:n.1272+151_1273-144delinsAGGGTACTTT
ENST00000260795.8:c.*322+151_*323-144delinsAGGGTACTTT	ENSP00000260795.3:n.*322+151_*323-144delinsAGGGTACTTT
ENST00000352904.6:c.931-153_931-144delinsAGGGTACTTT	ENSP00000231803.1:n.931-153_931-144delinsAGGGTACTTT
ENST00000412135.7:c.1254+151_1255-144delinsAGGGTACTTT	ENSP00000412903.3:n.1254+151_1255-144delinsAGGGTACTTT
ENST00000440486.8:c.1266+151_1267-144delinsAGGGTACTTT MANE Select	ENSP00000414914.2:n.1266+151_1267-144delinsAGGGTACTTT
ENST00000481110.7:c.1267-150_1267-141delinsAGGGTACTTT	ENSP00000420533.2:n.1267-150_1267-141delinsAGGGTACTTT
ENST00000260795.6:c.1266+151_1267-144delinsAGGGTACTTT	ENSP00000260795.2:n.1266+151_1267-144delinsAGGGTACTTT
ENST00000340107.8:c.1272+151_1273-144delinsAGGGTACTTT	ENSP00000339824.4:n.1272+151_1273-144delinsAGGGTACTTT
ENST00000352904.5:c.931-153_931-144delinsAGGGTACTTT	ENSP00000231803.1:n.931-153_931-144delinsAGGGTACTTT
ENST00000412135.6:c.931-153_931-144delinsAGGGTACTTT	ENSP00000412903.2:n.931-153_931-144delinsAGGGTACTTT
ENST00000440486.6:c.1266+151_1267-144delinsAGGGTACTTT	ENSP00000414914.2:n.1266+151_1267-144delinsAGGGTACTTT
ENST00000469068.1:n.180_189delinsAGGGTACTTT
ENST00000481110.6:c.1267-150_1267-141delinsAGGGTACTTT	ENSP00000420533.2:n.1267-150_1267-141delinsAGGGTACTTT
ENST00000613647.4:c.*322+151_*323-144delinsAGGGTACTTT	ENSP00000479472.1:n.*322+151_*323-144delinsAGGGTACTTT
NM_000142.4:c.1266+151_1267-144delinsAGGGTACTTT , LRG_1021t1:c.1266+151_1267-144delinsAGGGTACTTT	NP_000133.1:n.1266+151_1267-144delinsAGGGTACTTT
NM_001163213.1:c.1272+151_1273-144delinsAGGGTACTTT , LRG_1021t2:c.1272+151_1273-144delinsAGGGTACTTT	NP_001156685.1:n.1272+151_1273-144delinsAGGGTACTTT
NM_022965.3:c.931-153_931-144delinsAGGGTACTTT	NP_075254.1:n.931-153_931-144delinsAGGGTACTTT
XM_006713868.1:c.1278+145_1279-144delinsAGGGTACTTT	XP_006713931.1:n.1278+145_1279-144delinsAGGGTACTTT
XM_006713869.1:c.1278+145_1279-144delinsAGGGTACTTT	XP_006713932.1:n.1278+145_1279-144delinsAGGGTACTTT
XM_006713870.1:c.1273-150_1273-141delinsAGGGTACTTT	XP_006713933.1:n.1273-150_1273-141delinsAGGGTACTTT
XM_006713871.1:c.1272+151_1273-144delinsAGGGTACTTT	XP_006713934.1:n.1272+151_1273-144delinsAGGGTACTTT
XM_006713872.1:c.1267-150_1267-141delinsAGGGTACTTT	XP_006713935.1:n.1267-150_1267-141delinsAGGGTACTTT
XM_006713873.1:c.1266+151_1267-144delinsAGGGTACTTT	XP_006713936.1:n.1266+151_1267-144delinsAGGGTACTTT
XM_011513420.1:c.1272+145_1273-144delinsAGGGTACTTT	XP_011511722.1:n.1272+145_1273-144delinsAGGGTACTTT
XM_011513422.1:c.1267-150_1267-141delinsAGGGTACTTT	XP_011511724.1:n.1267-150_1267-141delinsAGGGTACTTT
NM_001354809.1:c.1267-150_1267-141delinsAGGGTACTTT	NP_001341738.1:n.1267-150_1267-141delinsAGGGTACTTT
NM_001354810.1:c.1267-150_1267-141delinsAGGGTACTTT	NP_001341739.1:n.1267-150_1267-141delinsAGGGTACTTT
NR_148971.1:n.1673+151_1674-144delinsAGGGTACTTT
NM_001354809.2:c.1267-150_1267-141delinsAGGGTACTTT	NP_001341738.1:n.1267-150_1267-141delinsAGGGTACTTT
NM_001354810.2:c.1267-150_1267-141delinsAGGGTACTTT	NP_001341739.1:n.1267-150_1267-141delinsAGGGTACTTT
NR_148971.2:n.1692+151_1693-144delinsAGGGTACTTT
NM_000142.5:c.1266+151_1267-144delinsAGGGTACTTT MANE Select	NP_000133.1:n.1266+151_1267-144delinsAGGGTACTTT
NM_001163213.2:c.1272+151_1273-144delinsAGGGTACTTT	NP_001156685.1:n.1272+151_1273-144delinsAGGGTACTTT
NM_022965.4:c.931-153_931-144delinsAGGGTACTTT	NP_075254.1:n.931-153_931-144delinsAGGGTACTTT