Canonical Allele Identifier: CA2669552077

Gene: FGFR3

Linked Data

• gnomAD v4: 4-1803970-C-CTG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1803973_1803974dup , CM000666.2:g.1803973_1803974dup	GRCh38
NC_000004.11:g.1805700_1805701dup , CM000666.1:g.1805700_1805701dup	GRCh37
NC_000004.10:g.1775498_1775499dup	NCBI36
NG_012632.1:g.15662_15663dup , LRG_1021:g.15662_15663dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340107.9:c.1082-357_1082-356dup	ENSP00000339824.4:n.1082-357_1082-356dup
ENST00000260795.8:c.*131+137_*131+138dup	ENSP00000260795.3:n.*131+137_*131+138dup
ENST00000352904.6:c.931-851_931-850dup	ENSP00000231803.1:n.931-851_931-850dup
ENST00000412135.7:c.1063+137_1063+138dup	ENSP00000412903.3:n.1063+137_1063+138dup
ENST00000440486.8:c.1075+137_1075+138dup MANE Select	ENSP00000414914.2:n.1075+137_1075+138dup
ENST00000481110.7:c.1075+137_1075+138dup	ENSP00000420533.2:n.1075+137_1075+138dup
ENST00000643463.1:n.227-357_227-356dup
ENST00000260795.6:c.1075+137_1075+138dup	ENSP00000260795.2:n.1075+137_1075+138dup
ENST00000340107.8:c.1082-357_1082-356dup	ENSP00000339824.4:n.1082-357_1082-356dup
ENST00000352904.5:c.931-851_931-850dup	ENSP00000231803.1:n.931-851_931-850dup
ENST00000412135.6:c.931-851_931-850dup	ENSP00000412903.2:n.931-851_931-850dup
ENST00000440486.6:c.1075+137_1075+138dup	ENSP00000414914.2:n.1075+137_1075+138dup
ENST00000481110.6:c.1075+137_1075+138dup	ENSP00000420533.2:n.1075+137_1075+138dup
ENST00000613647.4:c.*131+137_*131+138dup	ENSP00000479472.1:n.*131+137_*131+138dup
NM_000142.4:c.1075+137_1075+138dup , LRG_1021t1:c.1075+137_1075+138dup	NP_000133.1:n.1075+137_1075+138dup
NM_001163213.1:c.1082-357_1082-356dup , LRG_1021t2:c.1082-357_1082-356dup	NP_001156685.1:n.1082-357_1082-356dup
NM_022965.3:c.931-851_931-850dup	NP_075254.1:n.931-851_931-850dup
XM_006713868.1:c.1082-357_1082-356dup	XP_006713931.1:n.1082-357_1082-356dup
XM_006713869.1:c.1082-357_1082-356dup	XP_006713932.1:n.1082-357_1082-356dup
XM_006713870.1:c.1082-357_1082-356dup	XP_006713933.1:n.1082-357_1082-356dup
XM_006713871.1:c.1082-357_1082-356dup	XP_006713934.1:n.1082-357_1082-356dup
XM_006713872.1:c.1075+137_1075+138dup	XP_006713935.1:n.1075+137_1075+138dup
XM_006713873.1:c.1075+137_1075+138dup	XP_006713936.1:n.1075+137_1075+138dup
XM_011513420.1:c.1075+137_1075+138dup	XP_011511722.1:n.1075+137_1075+138dup
XM_011513422.1:c.1075+137_1075+138dup	XP_011511724.1:n.1075+137_1075+138dup
NM_001354809.1:c.1075+137_1075+138dup	NP_001341738.1:n.1075+137_1075+138dup
NM_001354810.1:c.1075+137_1075+138dup	NP_001341739.1:n.1075+137_1075+138dup
NR_148971.1:n.1482+137_1482+138dup
NM_001354809.2:c.1075+137_1075+138dup	NP_001341738.1:n.1075+137_1075+138dup
NM_001354810.2:c.1075+137_1075+138dup	NP_001341739.1:n.1075+137_1075+138dup
NR_148971.2:n.1501+137_1501+138dup
NM_000142.5:c.1075+137_1075+138dup MANE Select	NP_000133.1:n.1075+137_1075+138dup
NM_001163213.2:c.1082-357_1082-356dup	NP_001156685.1:n.1082-357_1082-356dup
NM_022965.4:c.931-851_931-850dup	NP_075254.1:n.931-851_931-850dup