Canonical Allele Identifier: CA1433506640

Gene: FGFR3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1804283_1804284delinsCG , CM000666.2:g.1804283_1804284delinsCG	GRCh38
NC_000004.11:g.1806010_1806011delinsCG , CM000666.1:g.1806010_1806011delinsCG	GRCh37
NC_000004.10:g.1775808_1775809delinsCG	NCBI36
NG_012632.1:g.15972_15973delinsCG , LRG_1021:g.15972_15973delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340107.9:c.1082-47_1082-46delinsCG	ENSP00000339824.4:n.1082-47_1082-46delinsCG
ENST00000260795.8:c.*132-47_*132-46delinsCG	ENSP00000260795.3:n.*132-47_*132-46delinsCG
ENST00000352904.6:c.931-541_931-540delinsCG	ENSP00000231803.1:n.931-541_931-540delinsCG
ENST00000412135.7:c.1064-47_1064-46delinsCG	ENSP00000412903.3:n.1064-47_1064-46delinsCG
ENST00000440486.8:c.1076-47_1076-46delinsCG MANE Select	ENSP00000414914.2:n.1076-47_1076-46delinsCG
ENST00000481110.7:c.1076-47_1076-46delinsCG	ENSP00000420533.2:n.1076-47_1076-46delinsCG
ENST00000643463.1:n.227-47_227-46delinsCG
ENST00000260795.6:c.1076-47_1076-46delinsCG	ENSP00000260795.2:n.1076-47_1076-46delinsCG
ENST00000340107.8:c.1082-47_1082-46delinsCG	ENSP00000339824.4:n.1082-47_1082-46delinsCG
ENST00000352904.5:c.931-541_931-540delinsCG	ENSP00000231803.1:n.931-541_931-540delinsCG
ENST00000412135.6:c.931-541_931-540delinsCG	ENSP00000412903.2:n.931-541_931-540delinsCG
ENST00000440486.6:c.1076-47_1076-46delinsCG	ENSP00000414914.2:n.1076-47_1076-46delinsCG
ENST00000481110.6:c.1076-47_1076-46delinsCG	ENSP00000420533.2:n.1076-47_1076-46delinsCG
ENST00000613647.4:c.*132-47_*132-46delinsCG	ENSP00000479472.1:n.*132-47_*132-46delinsCG
NM_000142.4:c.1076-47_1076-46delinsCG , LRG_1021t1:c.1076-47_1076-46delinsCG	NP_000133.1:n.1076-47_1076-46delinsCG
NM_001163213.1:c.1082-47_1082-46delinsCG , LRG_1021t2:c.1082-47_1082-46delinsCG	NP_001156685.1:n.1082-47_1082-46delinsCG
NM_022965.3:c.931-541_931-540delinsCG	NP_075254.1:n.931-541_931-540delinsCG
XM_006713868.1:c.1082-47_1082-46delinsCG	XP_006713931.1:n.1082-47_1082-46delinsCG
XM_006713869.1:c.1082-47_1082-46delinsCG	XP_006713932.1:n.1082-47_1082-46delinsCG
XM_006713870.1:c.1082-47_1082-46delinsCG	XP_006713933.1:n.1082-47_1082-46delinsCG
XM_006713871.1:c.1082-47_1082-46delinsCG	XP_006713934.1:n.1082-47_1082-46delinsCG
XM_006713872.1:c.1076-47_1076-46delinsCG	XP_006713935.1:n.1076-47_1076-46delinsCG
XM_006713873.1:c.1076-47_1076-46delinsCG	XP_006713936.1:n.1076-47_1076-46delinsCG
XM_011513420.1:c.1076-47_1076-46delinsCG	XP_011511722.1:n.1076-47_1076-46delinsCG
XM_011513422.1:c.1076-47_1076-46delinsCG	XP_011511724.1:n.1076-47_1076-46delinsCG
NM_001354809.1:c.1076-47_1076-46delinsCG	NP_001341738.1:n.1076-47_1076-46delinsCG
NM_001354810.1:c.1076-47_1076-46delinsCG	NP_001341739.1:n.1076-47_1076-46delinsCG
NR_148971.1:n.1483-47_1483-46delinsCG
NM_001354809.2:c.1076-47_1076-46delinsCG	NP_001341738.1:n.1076-47_1076-46delinsCG
NM_001354810.2:c.1076-47_1076-46delinsCG	NP_001341739.1:n.1076-47_1076-46delinsCG
NR_148971.2:n.1502-47_1502-46delinsCG
NM_000142.5:c.1076-47_1076-46delinsCG MANE Select	NP_000133.1:n.1076-47_1076-46delinsCG
NM_001163213.2:c.1082-47_1082-46delinsCG	NP_001156685.1:n.1082-47_1082-46delinsCG
NM_022965.4:c.931-541_931-540delinsCG	NP_075254.1:n.931-541_931-540delinsCG