Canonical Allele Identifier: CA2669552642

Gene: FGFR3

Linked Data

• gnomAD v4: 4-1804321-T-TCTTTG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1804323_1804327dup , CM000666.2:g.1804323_1804327dup	GRCh38
NC_000004.11:g.1806050_1806054dup , CM000666.1:g.1806050_1806054dup	GRCh37
NC_000004.10:g.1775848_1775852dup	NCBI36
NG_012632.1:g.16012_16016dup , LRG_1021:g.16012_16016dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000340107.9:c.1082-7_1082-3dup	ENSP00000339824.4:n.1082-7_1082-3dup
ENST00000260795.8:c.*132-7_*132-3dup	ENSP00000260795.3:n.*132-7_*132-3dup
ENST00000352904.6:c.931-501_931-497dup	ENSP00000231803.1:n.931-501_931-497dup
ENST00000412135.7:c.1064-7_1064-3dup	ENSP00000412903.3:n.1064-7_1064-3dup
ENST00000440486.8:c.1076-7_1076-3dup MANE Select	ENSP00000414914.2:n.1076-7_1076-3dup
ENST00000481110.7:c.1076-7_1076-3dup	ENSP00000420533.2:n.1076-7_1076-3dup
ENST00000643463.1:n.227-7_227-3dup
ENST00000260795.6:c.1076-7_1076-3dup	ENSP00000260795.2:n.1076-7_1076-3dup
ENST00000340107.8:c.1082-7_1082-3dup	ENSP00000339824.4:n.1082-7_1082-3dup
ENST00000352904.5:c.931-501_931-497dup	ENSP00000231803.1:n.931-501_931-497dup
ENST00000412135.6:c.931-501_931-497dup	ENSP00000412903.2:n.931-501_931-497dup
ENST00000440486.6:c.1076-7_1076-3dup	ENSP00000414914.2:n.1076-7_1076-3dup
ENST00000481110.6:c.1076-7_1076-3dup	ENSP00000420533.2:n.1076-7_1076-3dup
ENST00000613647.4:c.*132-7_*132-3dup	ENSP00000479472.1:n.*132-7_*132-3dup
NM_000142.4:c.1076-7_1076-3dup , LRG_1021t1:c.1076-7_1076-3dup	NP_000133.1:n.1076-7_1076-3dup
NM_001163213.1:c.1082-7_1082-3dup , LRG_1021t2:c.1082-7_1082-3dup	NP_001156685.1:n.1082-7_1082-3dup
NM_022965.3:c.931-501_931-497dup	NP_075254.1:n.931-501_931-497dup
XM_006713868.1:c.1082-7_1082-3dup	XP_006713931.1:n.1082-7_1082-3dup
XM_006713869.1:c.1082-7_1082-3dup	XP_006713932.1:n.1082-7_1082-3dup
XM_006713870.1:c.1082-7_1082-3dup	XP_006713933.1:n.1082-7_1082-3dup
XM_006713871.1:c.1082-7_1082-3dup	XP_006713934.1:n.1082-7_1082-3dup
XM_006713872.1:c.1076-7_1076-3dup	XP_006713935.1:n.1076-7_1076-3dup
XM_006713873.1:c.1076-7_1076-3dup	XP_006713936.1:n.1076-7_1076-3dup
XM_011513420.1:c.1076-7_1076-3dup	XP_011511722.1:n.1076-7_1076-3dup
XM_011513422.1:c.1076-7_1076-3dup	XP_011511724.1:n.1076-7_1076-3dup
NM_001354809.1:c.1076-7_1076-3dup	NP_001341738.1:n.1076-7_1076-3dup
NM_001354810.1:c.1076-7_1076-3dup	NP_001341739.1:n.1076-7_1076-3dup
NR_148971.1:n.1483-7_1483-3dup
NM_001354809.2:c.1076-7_1076-3dup	NP_001341738.1:n.1076-7_1076-3dup
NM_001354810.2:c.1076-7_1076-3dup	NP_001341739.1:n.1076-7_1076-3dup
NR_148971.2:n.1502-7_1502-3dup
NM_000142.5:c.1076-7_1076-3dup MANE Select	NP_000133.1:n.1076-7_1076-3dup
NM_001163213.2:c.1082-7_1082-3dup	NP_001156685.1:n.1082-7_1082-3dup
NM_022965.4:c.931-501_931-497dup	NP_075254.1:n.931-501_931-497dup