Canonical Allele Identifier: CA1433506652

Gene: FGFR3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1804288_1804290delinsGGG , CM000666.2:g.1804288_1804290delinsGGG	GRCh38
NC_000004.11:g.1806015_1806017delinsGGG , CM000666.1:g.1806015_1806017delinsGGG	GRCh37
NC_000004.10:g.1775813_1775815delinsGGG	NCBI36
NG_012632.1:g.15977_15979delinsGGG , LRG_1021:g.15977_15979delinsGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340107.9:c.1082-42_1082-40delinsGGG	ENSP00000339824.4:n.1082-42_1082-40delinsGGG
ENST00000260795.8:c.*132-42_*132-40delinsGGG	ENSP00000260795.3:n.*132-42_*132-40delinsGGG
ENST00000352904.6:c.931-536_931-534delinsGGG	ENSP00000231803.1:n.931-536_931-534delinsGGG
ENST00000412135.7:c.1064-42_1064-40delinsGGG	ENSP00000412903.3:n.1064-42_1064-40delinsGGG
ENST00000440486.8:c.1076-42_1076-40delinsGGG MANE Select	ENSP00000414914.2:n.1076-42_1076-40delinsGGG
ENST00000481110.7:c.1076-42_1076-40delinsGGG	ENSP00000420533.2:n.1076-42_1076-40delinsGGG
ENST00000643463.1:n.227-42_227-40delinsGGG
ENST00000260795.6:c.1076-42_1076-40delinsGGG	ENSP00000260795.2:n.1076-42_1076-40delinsGGG
ENST00000340107.8:c.1082-42_1082-40delinsGGG	ENSP00000339824.4:n.1082-42_1082-40delinsGGG
ENST00000352904.5:c.931-536_931-534delinsGGG	ENSP00000231803.1:n.931-536_931-534delinsGGG
ENST00000412135.6:c.931-536_931-534delinsGGG	ENSP00000412903.2:n.931-536_931-534delinsGGG
ENST00000440486.6:c.1076-42_1076-40delinsGGG	ENSP00000414914.2:n.1076-42_1076-40delinsGGG
ENST00000481110.6:c.1076-42_1076-40delinsGGG	ENSP00000420533.2:n.1076-42_1076-40delinsGGG
ENST00000613647.4:c.*132-42_*132-40delinsGGG	ENSP00000479472.1:n.*132-42_*132-40delinsGGG
NM_000142.4:c.1076-42_1076-40delinsGGG , LRG_1021t1:c.1076-42_1076-40delinsGGG	NP_000133.1:n.1076-42_1076-40delinsGGG
NM_001163213.1:c.1082-42_1082-40delinsGGG , LRG_1021t2:c.1082-42_1082-40delinsGGG	NP_001156685.1:n.1082-42_1082-40delinsGGG
NM_022965.3:c.931-536_931-534delinsGGG	NP_075254.1:n.931-536_931-534delinsGGG
XM_006713868.1:c.1082-42_1082-40delinsGGG	XP_006713931.1:n.1082-42_1082-40delinsGGG
XM_006713869.1:c.1082-42_1082-40delinsGGG	XP_006713932.1:n.1082-42_1082-40delinsGGG
XM_006713870.1:c.1082-42_1082-40delinsGGG	XP_006713933.1:n.1082-42_1082-40delinsGGG
XM_006713871.1:c.1082-42_1082-40delinsGGG	XP_006713934.1:n.1082-42_1082-40delinsGGG
XM_006713872.1:c.1076-42_1076-40delinsGGG	XP_006713935.1:n.1076-42_1076-40delinsGGG
XM_006713873.1:c.1076-42_1076-40delinsGGG	XP_006713936.1:n.1076-42_1076-40delinsGGG
XM_011513420.1:c.1076-42_1076-40delinsGGG	XP_011511722.1:n.1076-42_1076-40delinsGGG
XM_011513422.1:c.1076-42_1076-40delinsGGG	XP_011511724.1:n.1076-42_1076-40delinsGGG
NM_001354809.1:c.1076-42_1076-40delinsGGG	NP_001341738.1:n.1076-42_1076-40delinsGGG
NM_001354810.1:c.1076-42_1076-40delinsGGG	NP_001341739.1:n.1076-42_1076-40delinsGGG
NR_148971.1:n.1483-42_1483-40delinsGGG
NM_001354809.2:c.1076-42_1076-40delinsGGG	NP_001341738.1:n.1076-42_1076-40delinsGGG
NM_001354810.2:c.1076-42_1076-40delinsGGG	NP_001341739.1:n.1076-42_1076-40delinsGGG
NR_148971.2:n.1502-42_1502-40delinsGGG
NM_000142.5:c.1076-42_1076-40delinsGGG MANE Select	NP_000133.1:n.1076-42_1076-40delinsGGG
NM_001163213.2:c.1082-42_1082-40delinsGGG	NP_001156685.1:n.1082-42_1082-40delinsGGG
NM_022965.4:c.931-536_931-534delinsGGG	NP_075254.1:n.931-536_931-534delinsGGG