Canonical Allele Identifier: CA791736218

Gene: FGFR3

Linked Data

• dbSNP Id: rs1553846871
• MyVariant Identifiers: chr4:g.1806010_1806011insTT (hg19) ; chr4:g.1804283_1804284insTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1804283_1804284insTT , CM000666.2:g.1804283_1804284insTT	GRCh38
NC_000004.11:g.1806010_1806011insTT , CM000666.1:g.1806010_1806011insTT	GRCh37
NC_000004.10:g.1775808_1775809insTT	NCBI36
NG_012632.1:g.15972_15973insTT , LRG_1021:g.15972_15973insTT

Transcript Alleles

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