Canonical Allele Identifier: CA2669552414

Gene: FGFR3

Linked Data

• gnomAD v4: 4-1804286-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1804286_1804287insT , CM000666.2:g.1804286_1804287insT	GRCh38
NC_000004.11:g.1806013_1806014insT , CM000666.1:g.1806013_1806014insT	GRCh37
NC_000004.10:g.1775811_1775812insT	NCBI36
NG_012632.1:g.15975_15976insT , LRG_1021:g.15975_15976insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340107.9:c.1082-44_1082-43insT	ENSP00000339824.4:n.1082-44_1082-43insT
ENST00000260795.8:c.*132-44_*132-43insT	ENSP00000260795.3:n.*132-44_*132-43insT
ENST00000352904.6:c.931-538_931-537insT	ENSP00000231803.1:n.931-538_931-537insT
ENST00000412135.7:c.1064-44_1064-43insT	ENSP00000412903.3:n.1064-44_1064-43insT
ENST00000440486.8:c.1076-44_1076-43insT MANE Select	ENSP00000414914.2:n.1076-44_1076-43insT
ENST00000481110.7:c.1076-44_1076-43insT	ENSP00000420533.2:n.1076-44_1076-43insT
ENST00000643463.1:n.227-44_227-43insT
ENST00000260795.6:c.1076-44_1076-43insT	ENSP00000260795.2:n.1076-44_1076-43insT
ENST00000340107.8:c.1082-44_1082-43insT	ENSP00000339824.4:n.1082-44_1082-43insT
ENST00000352904.5:c.931-538_931-537insT	ENSP00000231803.1:n.931-538_931-537insT
ENST00000412135.6:c.931-538_931-537insT	ENSP00000412903.2:n.931-538_931-537insT
ENST00000440486.6:c.1076-44_1076-43insT	ENSP00000414914.2:n.1076-44_1076-43insT
ENST00000481110.6:c.1076-44_1076-43insT	ENSP00000420533.2:n.1076-44_1076-43insT
ENST00000613647.4:c.*132-44_*132-43insT	ENSP00000479472.1:n.*132-44_*132-43insT
NM_000142.4:c.1076-44_1076-43insT , LRG_1021t1:c.1076-44_1076-43insT	NP_000133.1:n.1076-44_1076-43insT
NM_001163213.1:c.1082-44_1082-43insT , LRG_1021t2:c.1082-44_1082-43insT	NP_001156685.1:n.1082-44_1082-43insT
NM_022965.3:c.931-538_931-537insT	NP_075254.1:n.931-538_931-537insT
XM_006713868.1:c.1082-44_1082-43insT	XP_006713931.1:n.1082-44_1082-43insT
XM_006713869.1:c.1082-44_1082-43insT	XP_006713932.1:n.1082-44_1082-43insT
XM_006713870.1:c.1082-44_1082-43insT	XP_006713933.1:n.1082-44_1082-43insT
XM_006713871.1:c.1082-44_1082-43insT	XP_006713934.1:n.1082-44_1082-43insT
XM_006713872.1:c.1076-44_1076-43insT	XP_006713935.1:n.1076-44_1076-43insT
XM_006713873.1:c.1076-44_1076-43insT	XP_006713936.1:n.1076-44_1076-43insT
XM_011513420.1:c.1076-44_1076-43insT	XP_011511722.1:n.1076-44_1076-43insT
XM_011513422.1:c.1076-44_1076-43insT	XP_011511724.1:n.1076-44_1076-43insT
NM_001354809.1:c.1076-44_1076-43insT	NP_001341738.1:n.1076-44_1076-43insT
NM_001354810.1:c.1076-44_1076-43insT	NP_001341739.1:n.1076-44_1076-43insT
NR_148971.1:n.1483-44_1483-43insT
NM_001354809.2:c.1076-44_1076-43insT	NP_001341738.1:n.1076-44_1076-43insT
NM_001354810.2:c.1076-44_1076-43insT	NP_001341739.1:n.1076-44_1076-43insT
NR_148971.2:n.1502-44_1502-43insT
NM_000142.5:c.1076-44_1076-43insT MANE Select	NP_000133.1:n.1076-44_1076-43insT
NM_001163213.2:c.1082-44_1082-43insT	NP_001156685.1:n.1082-44_1082-43insT
NM_022965.4:c.931-538_931-537insT	NP_075254.1:n.931-538_931-537insT