Canonical Allele Identifier: CA2669552596

Gene: FGFR3

Linked Data

• gnomAD v4: 4-1804307-C-CGTTG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1804307_1804308insGTTG , CM000666.2:g.1804307_1804308insGTTG	GRCh38
NC_000004.11:g.1806034_1806035insGTTG , CM000666.1:g.1806034_1806035insGTTG	GRCh37
NC_000004.10:g.1775832_1775833insGTTG	NCBI36
NG_012632.1:g.15996_15997insGTTG , LRG_1021:g.15996_15997insGTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340107.9:c.1082-23_1082-22insGTTG	ENSP00000339824.4:n.1082-23_1082-22insGTTG
ENST00000260795.8:c.*132-23_*132-22insGTTG	ENSP00000260795.3:n.*132-23_*132-22insGTTG
ENST00000352904.6:c.931-517_931-516insGTTG	ENSP00000231803.1:n.931-517_931-516insGTTG
ENST00000412135.7:c.1064-23_1064-22insGTTG	ENSP00000412903.3:n.1064-23_1064-22insGTTG
ENST00000440486.8:c.1076-23_1076-22insGTTG MANE Select	ENSP00000414914.2:n.1076-23_1076-22insGTTG
ENST00000481110.7:c.1076-23_1076-22insGTTG	ENSP00000420533.2:n.1076-23_1076-22insGTTG
ENST00000643463.1:n.227-23_227-22insGTTG
ENST00000260795.6:c.1076-23_1076-22insGTTG	ENSP00000260795.2:n.1076-23_1076-22insGTTG
ENST00000340107.8:c.1082-23_1082-22insGTTG	ENSP00000339824.4:n.1082-23_1082-22insGTTG
ENST00000352904.5:c.931-517_931-516insGTTG	ENSP00000231803.1:n.931-517_931-516insGTTG
ENST00000412135.6:c.931-517_931-516insGTTG	ENSP00000412903.2:n.931-517_931-516insGTTG
ENST00000440486.6:c.1076-23_1076-22insGTTG	ENSP00000414914.2:n.1076-23_1076-22insGTTG
ENST00000481110.6:c.1076-23_1076-22insGTTG	ENSP00000420533.2:n.1076-23_1076-22insGTTG
ENST00000613647.4:c.*132-23_*132-22insGTTG	ENSP00000479472.1:n.*132-23_*132-22insGTTG
NM_000142.4:c.1076-23_1076-22insGTTG , LRG_1021t1:c.1076-23_1076-22insGTTG	NP_000133.1:n.1076-23_1076-22insGTTG
NM_001163213.1:c.1082-23_1082-22insGTTG , LRG_1021t2:c.1082-23_1082-22insGTTG	NP_001156685.1:n.1082-23_1082-22insGTTG
NM_022965.3:c.931-517_931-516insGTTG	NP_075254.1:n.931-517_931-516insGTTG
XM_006713868.1:c.1082-23_1082-22insGTTG	XP_006713931.1:n.1082-23_1082-22insGTTG
XM_006713869.1:c.1082-23_1082-22insGTTG	XP_006713932.1:n.1082-23_1082-22insGTTG
XM_006713870.1:c.1082-23_1082-22insGTTG	XP_006713933.1:n.1082-23_1082-22insGTTG
XM_006713871.1:c.1082-23_1082-22insGTTG	XP_006713934.1:n.1082-23_1082-22insGTTG
XM_006713872.1:c.1076-23_1076-22insGTTG	XP_006713935.1:n.1076-23_1076-22insGTTG
XM_006713873.1:c.1076-23_1076-22insGTTG	XP_006713936.1:n.1076-23_1076-22insGTTG
XM_011513420.1:c.1076-23_1076-22insGTTG	XP_011511722.1:n.1076-23_1076-22insGTTG
XM_011513422.1:c.1076-23_1076-22insGTTG	XP_011511724.1:n.1076-23_1076-22insGTTG
NM_001354809.1:c.1076-23_1076-22insGTTG	NP_001341738.1:n.1076-23_1076-22insGTTG
NM_001354810.1:c.1076-23_1076-22insGTTG	NP_001341739.1:n.1076-23_1076-22insGTTG
NR_148971.1:n.1483-23_1483-22insGTTG
NM_001354809.2:c.1076-23_1076-22insGTTG	NP_001341738.1:n.1076-23_1076-22insGTTG
NM_001354810.2:c.1076-23_1076-22insGTTG	NP_001341739.1:n.1076-23_1076-22insGTTG
NR_148971.2:n.1502-23_1502-22insGTTG
NM_000142.5:c.1076-23_1076-22insGTTG MANE Select	NP_000133.1:n.1076-23_1076-22insGTTG
NM_001163213.2:c.1082-23_1082-22insGTTG	NP_001156685.1:n.1082-23_1082-22insGTTG
NM_022965.4:c.931-517_931-516insGTTG	NP_075254.1:n.931-517_931-516insGTTG