Canonical Allele Identifier: CA1433506681

Gene: FGFR3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1804333_1804345delinsAGGAGGAGCTGGT , CM000666.2:g.1804333_1804345delinsAGGAGGAGCTGGT	GRCh38
NC_000004.11:g.1806060_1806072delinsAGGAGGAGCTGGT , CM000666.1:g.1806060_1806072delinsAGGAGGAGCTGGT	GRCh37
NC_000004.10:g.1775858_1775870delinsAGGAGGAGCTGGT	NCBI36
NG_012632.1:g.16022_16034delinsAGGAGGAGCTGGT , LRG_1021:g.16022_16034delinsAGGAGGAGCTGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340107.9:c.1085_1097delinsAGGAGGAGCTGGT	ENSP00000339824.4:p.Glu362=
ENST00000260795.8:c.*135_*147delinsAGGAGGAGCTGGT	ENSP00000260795.3:n.*135_*147delinsAGGAGGAGCTGGT
ENST00000352904.6:c.931-491_931-479delinsAGGAGGAGCTGGT	ENSP00000231803.1:n.931-491_931-479delinsAGGAGGAGCTGGT
ENST00000412135.7:c.1067_1079delinsAGGAGGAGCTGGT	ENSP00000412903.3:p.Glu356=
ENST00000440486.8:c.1079_1091delinsAGGAGGAGCTGGT MANE Select	ENSP00000414914.2:p.Glu360=
ENST00000481110.7:c.1079_1091delinsAGGAGGAGCTGGT	ENSP00000420533.2:p.Glu360=
ENST00000643463.1:n.230_242delinsAGGAGGAGCTGGT
ENST00000260795.6:c.1079_1091delinsAGGAGGAGCTGGT	ENSP00000260795.2:p.Glu360=
ENST00000340107.8:c.1085_1097delinsAGGAGGAGCTGGT	ENSP00000339824.4:p.Glu362=
ENST00000352904.5:c.931-491_931-479delinsAGGAGGAGCTGGT	ENSP00000231803.1:n.931-491_931-479delinsAGGAGGAGCTGGT
ENST00000412135.6:c.931-491_931-479delinsAGGAGGAGCTGGT	ENSP00000412903.2:n.931-491_931-479delinsAGGAGGAGCTGGT
ENST00000440486.6:c.1079_1091delinsAGGAGGAGCTGGT	ENSP00000414914.2:p.Glu360=
ENST00000481110.6:c.1079_1091delinsAGGAGGAGCTGGT	ENSP00000420533.2:p.Glu360=
ENST00000613647.4:c.*135_*147delinsAGGAGGAGCTGGT	ENSP00000479472.1:n.*135_*147delinsAGGAGGAGCTGGT
NM_000142.4:c.1079_1091delinsAGGAGGAGCTGGT , LRG_1021t1:c.1079_1091delinsAGGAGGAGCTGGT	NP_000133.1:p.Glu360=
NM_001163213.1:c.1085_1097delinsAGGAGGAGCTGGT , LRG_1021t2:c.1085_1097delinsAGGAGGAGCTGGT	NP_001156685.1:p.Glu362=
NM_022965.3:c.931-491_931-479delinsAGGAGGAGCTGGT	NP_075254.1:n.931-491_931-479delinsAGGAGGAGCTGGT
XM_006713868.1:c.1085_1097delinsAGGAGGAGCTGGT	XP_006713931.1:p.Glu362=
XM_006713869.1:c.1085_1097delinsAGGAGGAGCTGGT	XP_006713932.1:p.Glu362=
XM_006713870.1:c.1085_1097delinsAGGAGGAGCTGGT	XP_006713933.1:p.Glu362=
XM_006713871.1:c.1085_1097delinsAGGAGGAGCTGGT	XP_006713934.1:p.Glu362=
XM_006713872.1:c.1079_1091delinsAGGAGGAGCTGGT	XP_006713935.1:p.Glu360=
XM_006713873.1:c.1079_1091delinsAGGAGGAGCTGGT	XP_006713936.1:p.Glu360=
XM_011513420.1:c.1079_1091delinsAGGAGGAGCTGGT	XP_011511722.1:p.Glu360=
XM_011513422.1:c.1079_1091delinsAGGAGGAGCTGGT	XP_011511724.1:p.Glu360=
NM_001354809.1:c.1079_1091delinsAGGAGGAGCTGGT	NP_001341738.1:p.Glu360=
NM_001354810.1:c.1079_1091delinsAGGAGGAGCTGGT	NP_001341739.1:p.Glu360=
NR_148971.1:n.1486_1498delinsAGGAGGAGCTGGT
NM_001354809.2:c.1079_1091delinsAGGAGGAGCTGGT	NP_001341738.1:p.Glu360=
NM_001354810.2:c.1079_1091delinsAGGAGGAGCTGGT	NP_001341739.1:p.Glu360=
NR_148971.2:n.1505_1517delinsAGGAGGAGCTGGT
NM_000142.5:c.1079_1091delinsAGGAGGAGCTGGT MANE Select	NP_000133.1:p.Glu360=
NM_001163213.2:c.1085_1097delinsAGGAGGAGCTGGT	NP_001156685.1:p.Glu362=
NM_022965.4:c.931-491_931-479delinsAGGAGGAGCTGGT	NP_075254.1:n.931-491_931-479delinsAGGAGGAGCTGGT