Canonical Allele Identifier: CA1433506889

Gene: FGFR3

Linked Data

• dbSNP Id: rs1721647582

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1804659_1804660insTAGGGTG , CM000666.2:g.1804659_1804660insTAGGGTG	GRCh38
NC_000004.11:g.1806386_1806387insTAGGGTG , CM000666.1:g.1806386_1806387insTAGGGTG	GRCh37
NC_000004.10:g.1776184_1776185insTAGGGTG	NCBI36
NG_012632.1:g.16348_16349insTAGGGTG , LRG_1021:g.16348_16349insTAGGGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340107.9:c.1272+139_1272+140insTAGGGTG	ENSP00000339824.4:n.1272+139_1272+140insTAGGGTG
ENST00000260795.8:c.*322+139_*322+140insTAGGGTG	ENSP00000260795.3:n.*322+139_*322+140insTAGGGTG
ENST00000352904.6:c.931-165_931-164insTAGGGTG	ENSP00000231803.1:n.931-165_931-164insTAGGGTG
ENST00000412135.7:c.1254+139_1254+140insTAGGGTG	ENSP00000412903.3:n.1254+139_1254+140insTAGGGTG
ENST00000440486.8:c.1266+139_1266+140insTAGGGTG MANE Select	ENSP00000414914.2:n.1266+139_1266+140insTAGGGTG
ENST00000481110.7:c.1266+139_1266+140insTAGGGTG	ENSP00000420533.2:n.1266+139_1266+140insTAGGGTG
ENST00000260795.6:c.1266+139_1266+140insTAGGGTG	ENSP00000260795.2:n.1266+139_1266+140insTAGGGTG
ENST00000340107.8:c.1272+139_1272+140insTAGGGTG	ENSP00000339824.4:n.1272+139_1272+140insTAGGGTG
ENST00000352904.5:c.931-165_931-164insTAGGGTG	ENSP00000231803.1:n.931-165_931-164insTAGGGTG
ENST00000412135.6:c.931-165_931-164insTAGGGTG	ENSP00000412903.2:n.931-165_931-164insTAGGGTG
ENST00000440486.6:c.1266+139_1266+140insTAGGGTG	ENSP00000414914.2:n.1266+139_1266+140insTAGGGTG
ENST00000469068.1:n.168_169insTAGGGTG
ENST00000481110.6:c.1266+139_1266+140insTAGGGTG	ENSP00000420533.2:n.1266+139_1266+140insTAGGGTG
ENST00000613647.4:c.*322+139_*322+140insTAGGGTG	ENSP00000479472.1:n.*322+139_*322+140insTAGGGTG
NM_000142.4:c.1266+139_1266+140insTAGGGTG , LRG_1021t1:c.1266+139_1266+140insTAGGGTG	NP_000133.1:n.1266+139_1266+140insTAGGGTG
NM_001163213.1:c.1272+139_1272+140insTAGGGTG , LRG_1021t2:c.1272+139_1272+140insTAGGGTG	NP_001156685.1:n.1272+139_1272+140insTAGGGTG
NM_022965.3:c.931-165_931-164insTAGGGTG	NP_075254.1:n.931-165_931-164insTAGGGTG
XM_006713868.1:c.1278+133_1278+134insTAGGGTG	XP_006713931.1:n.1278+133_1278+134insTAGGGTG
XM_006713869.1:c.1278+133_1278+134insTAGGGTG	XP_006713932.1:n.1278+133_1278+134insTAGGGTG
XM_006713870.1:c.1272+139_1272+140insTAGGGTG	XP_006713933.1:n.1272+139_1272+140insTAGGGTG
XM_006713871.1:c.1272+139_1272+140insTAGGGTG	XP_006713934.1:n.1272+139_1272+140insTAGGGTG
XM_006713872.1:c.1266+139_1266+140insTAGGGTG	XP_006713935.1:n.1266+139_1266+140insTAGGGTG
XM_006713873.1:c.1266+139_1266+140insTAGGGTG	XP_006713936.1:n.1266+139_1266+140insTAGGGTG
XM_011513420.1:c.1272+133_1272+134insTAGGGTG	XP_011511722.1:n.1272+133_1272+134insTAGGGTG
XM_011513422.1:c.1266+139_1266+140insTAGGGTG	XP_011511724.1:n.1266+139_1266+140insTAGGGTG
NM_001354809.1:c.1266+139_1266+140insTAGGGTG	NP_001341738.1:n.1266+139_1266+140insTAGGGTG
NM_001354810.1:c.1266+139_1266+140insTAGGGTG	NP_001341739.1:n.1266+139_1266+140insTAGGGTG
NR_148971.1:n.1673+139_1673+140insTAGGGTG
NM_001354809.2:c.1266+139_1266+140insTAGGGTG	NP_001341738.1:n.1266+139_1266+140insTAGGGTG
NM_001354810.2:c.1266+139_1266+140insTAGGGTG	NP_001341739.1:n.1266+139_1266+140insTAGGGTG
NR_148971.2:n.1692+139_1692+140insTAGGGTG
NM_000142.5:c.1266+139_1266+140insTAGGGTG MANE Select	NP_000133.1:n.1266+139_1266+140insTAGGGTG
NM_001163213.2:c.1272+139_1272+140insTAGGGTG	NP_001156685.1:n.1272+139_1272+140insTAGGGTG
NM_022965.4:c.931-165_931-164insTAGGGTG	NP_075254.1:n.931-165_931-164insTAGGGTG