Canonical Allele Identifier: CA2669553086

Gene: FGFR3

Linked Data

• gnomAD v4: 4-1804593-C-CTGG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1804595_1804597dup , CM000666.2:g.1804595_1804597dup	GRCh38
NC_000004.11:g.1806322_1806324dup , CM000666.1:g.1806322_1806324dup	GRCh37
NC_000004.10:g.1776120_1776122dup	NCBI36
NG_012632.1:g.16284_16286dup , LRG_1021:g.16284_16286dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340107.9:c.1272+75_1272+77dup	ENSP00000339824.4:n.1272+75_1272+77dup
ENST00000260795.8:c.*322+75_*322+77dup	ENSP00000260795.3:n.*322+75_*322+77dup
ENST00000352904.6:c.931-229_931-227dup	ENSP00000231803.1:n.931-229_931-227dup
ENST00000412135.7:c.1254+75_1254+77dup	ENSP00000412903.3:n.1254+75_1254+77dup
ENST00000440486.8:c.1266+75_1266+77dup MANE Select	ENSP00000414914.2:n.1266+75_1266+77dup
ENST00000481110.7:c.1266+75_1266+77dup	ENSP00000420533.2:n.1266+75_1266+77dup
ENST00000260795.6:c.1266+75_1266+77dup	ENSP00000260795.2:n.1266+75_1266+77dup
ENST00000340107.8:c.1272+75_1272+77dup	ENSP00000339824.4:n.1272+75_1272+77dup
ENST00000352904.5:c.931-229_931-227dup	ENSP00000231803.1:n.931-229_931-227dup
ENST00000412135.6:c.931-229_931-227dup	ENSP00000412903.2:n.931-229_931-227dup
ENST00000440486.6:c.1266+75_1266+77dup	ENSP00000414914.2:n.1266+75_1266+77dup
ENST00000469068.1:n.104_106dup
ENST00000481110.6:c.1266+75_1266+77dup	ENSP00000420533.2:n.1266+75_1266+77dup
ENST00000613647.4:c.*322+75_*322+77dup	ENSP00000479472.1:n.*322+75_*322+77dup
NM_000142.4:c.1266+75_1266+77dup , LRG_1021t1:c.1266+75_1266+77dup	NP_000133.1:n.1266+75_1266+77dup
NM_001163213.1:c.1272+75_1272+77dup , LRG_1021t2:c.1272+75_1272+77dup	NP_001156685.1:n.1272+75_1272+77dup
NM_022965.3:c.931-229_931-227dup	NP_075254.1:n.931-229_931-227dup
XM_006713868.1:c.1278+69_1278+71dup	XP_006713931.1:n.1278+69_1278+71dup
XM_006713869.1:c.1278+69_1278+71dup	XP_006713932.1:n.1278+69_1278+71dup
XM_006713870.1:c.1272+75_1272+77dup	XP_006713933.1:n.1272+75_1272+77dup
XM_006713871.1:c.1272+75_1272+77dup	XP_006713934.1:n.1272+75_1272+77dup
XM_006713872.1:c.1266+75_1266+77dup	XP_006713935.1:n.1266+75_1266+77dup
XM_006713873.1:c.1266+75_1266+77dup	XP_006713936.1:n.1266+75_1266+77dup
XM_011513420.1:c.1272+69_1272+71dup	XP_011511722.1:n.1272+69_1272+71dup
XM_011513422.1:c.1266+75_1266+77dup	XP_011511724.1:n.1266+75_1266+77dup
NM_001354809.1:c.1266+75_1266+77dup	NP_001341738.1:n.1266+75_1266+77dup
NM_001354810.1:c.1266+75_1266+77dup	NP_001341739.1:n.1266+75_1266+77dup
NR_148971.1:n.1673+75_1673+77dup
NM_001354809.2:c.1266+75_1266+77dup	NP_001341738.1:n.1266+75_1266+77dup
NM_001354810.2:c.1266+75_1266+77dup	NP_001341739.1:n.1266+75_1266+77dup
NR_148971.2:n.1692+75_1692+77dup
NM_000142.5:c.1266+75_1266+77dup MANE Select	NP_000133.1:n.1266+75_1266+77dup
NM_001163213.2:c.1272+75_1272+77dup	NP_001156685.1:n.1272+75_1272+77dup
NM_022965.4:c.931-229_931-227dup	NP_075254.1:n.931-229_931-227dup