Canonical Allele Identifier: CA2586965948

Gene: FGFR3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1804392_1804393delinsAA , CM000666.2:g.1804392_1804393delinsAA	GRCh38
NC_000004.11:g.1806119_1806120delinsAA , CM000666.1:g.1806119_1806120delinsAA	GRCh37
NC_000004.10:g.1775917_1775918delinsAA	NCBI36
NG_012632.1:g.16081_16082delinsAA , LRG_1021:g.16081_16082delinsAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340107.9:c.1144_1145delinsAA	ENSP00000339824.4:p.Gly382Lys
ENST00000260795.8:c.*194_*195delinsAA	ENSP00000260795.3:n.*194_*195delinsAA
ENST00000352904.6:c.931-432_931-431delinsAA	ENSP00000231803.1:n.931-432_931-431delinsAA
ENST00000412135.7:c.1126_1127delinsAA	ENSP00000412903.3:p.Gly376Lys
ENST00000440486.8:c.1138_1139delinsAA MANE Select	ENSP00000414914.2:p.Gly380Lys
ENST00000481110.7:c.1138_1139delinsAA	ENSP00000420533.2:p.Gly380Lys
ENST00000643463.1:n.289_290delinsAA
ENST00000260795.6:c.1138_1139delinsAA	ENSP00000260795.2:p.Gly380Lys
ENST00000340107.8:c.1144_1145delinsAA	ENSP00000339824.4:p.Gly382Lys
ENST00000352904.5:c.931-432_931-431delinsAA	ENSP00000231803.1:n.931-432_931-431delinsAA
ENST00000412135.6:c.931-432_931-431delinsAA	ENSP00000412903.2:n.931-432_931-431delinsAA
ENST00000440486.6:c.1138_1139delinsAA	ENSP00000414914.2:p.Gly380Lys
ENST00000481110.6:c.1138_1139delinsAA	ENSP00000420533.2:p.Gly380Lys
ENST00000613647.4:c.*194_*195delinsAA	ENSP00000479472.1:n.*194_*195delinsAA
NM_000142.4:c.1138_1139delinsAA , LRG_1021t1:c.1138_1139delinsAA	NP_000133.1:p.Gly380Lys
NM_001163213.1:c.1144_1145delinsAA , LRG_1021t2:c.1144_1145delinsAA	NP_001156685.1:p.Gly382Lys
NM_022965.3:c.931-432_931-431delinsAA	NP_075254.1:n.931-432_931-431delinsAA
XM_006713868.1:c.1144_1145delinsAA	XP_006713931.1:p.Gly382Lys
XM_006713869.1:c.1144_1145delinsAA	XP_006713932.1:p.Gly382Lys
XM_006713870.1:c.1144_1145delinsAA	XP_006713933.1:p.Gly382Lys
XM_006713871.1:c.1144_1145delinsAA	XP_006713934.1:p.Gly382Lys
XM_006713872.1:c.1138_1139delinsAA	XP_006713935.1:p.Gly380Lys
XM_006713873.1:c.1138_1139delinsAA	XP_006713936.1:p.Gly380Lys
XM_011513420.1:c.1138_1139delinsAA	XP_011511722.1:p.Gly380Lys
XM_011513422.1:c.1138_1139delinsAA	XP_011511724.1:p.Gly380Lys
NM_001354809.1:c.1138_1139delinsAA	NP_001341738.1:p.Gly380Lys
NM_001354810.1:c.1138_1139delinsAA	NP_001341739.1:p.Gly380Lys
NR_148971.1:n.1545_1546delinsAA
NM_001354809.2:c.1138_1139delinsAA	NP_001341738.1:p.Gly380Lys
NM_001354810.2:c.1138_1139delinsAA	NP_001341739.1:p.Gly380Lys
NR_148971.2:n.1564_1565delinsAA
NM_000142.5:c.1138_1139delinsAA MANE Select	NP_000133.1:p.Gly380Lys
NM_001163213.2:c.1144_1145delinsAA	NP_001156685.1:p.Gly382Lys
NM_022965.4:c.931-432_931-431delinsAA	NP_075254.1:n.931-432_931-431delinsAA