Canonical Allele Identifier: CA2810203

Gene: FGFR3

Linked Data

• ClinVar Variation Id: 1183225
• ClinVar RCV Id: RCV001541015
• dbSNP Id: rs4647926
• ExAC: 4:1806012 T / TG
• gnomAD v2: 4-1806012-T-TG
• gnomAD v3: 4-1804285-T-TG
• gnomAD v4: 4-1804285-T-TG
• MyVariant Identifiers: chr4:g.1806015_1806016insG (hg19) ; chr4:g.1806014_1806015insG (hg19) ; chr4:g.1806012_1806013insG (hg19) ; chr4:g.1804288_1804289insG (hg38) ; chr4:g.1804287_1804288insG (hg38) ; chr4:g.1804285_1804286insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1804296dup , CM000666.2:g.1804296dup	GRCh38
NC_000004.11:g.1806023dup , CM000666.1:g.1806023dup	GRCh37
NC_000004.10:g.1775821dup	NCBI36
NG_012632.1:g.15985dup , LRG_1021:g.15985dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000340107.9:c.1082-34dup	ENSP00000339824.4:n.1082-34dup
ENST00000260795.8:c.*132-34dup	ENSP00000260795.3:n.*132-34dup
ENST00000352904.6:c.931-528dup	ENSP00000231803.1:n.931-528dup
ENST00000412135.7:c.1064-34dup	ENSP00000412903.3:n.1064-34dup
ENST00000440486.8:c.1076-34dup MANE Select	ENSP00000414914.2:n.1076-34dup
ENST00000481110.7:c.1076-34dup	ENSP00000420533.2:n.1076-34dup
ENST00000643463.1:n.227-34dup
ENST00000260795.6:c.1076-34dup	ENSP00000260795.2:n.1076-34dup
ENST00000340107.8:c.1082-34dup	ENSP00000339824.4:n.1082-34dup
ENST00000352904.5:c.931-528dup	ENSP00000231803.1:n.931-528dup
ENST00000412135.6:c.931-528dup	ENSP00000412903.2:n.931-528dup
ENST00000440486.6:c.1076-34dup	ENSP00000414914.2:n.1076-34dup
ENST00000481110.6:c.1076-34dup	ENSP00000420533.2:n.1076-34dup
ENST00000613647.4:c.*132-34dup	ENSP00000479472.1:n.*132-34dup
NM_000142.4:c.1076-34dup , LRG_1021t1:c.1076-34dup	NP_000133.1:n.1076-34dup
NM_001163213.1:c.1082-34dup , LRG_1021t2:c.1082-34dup	NP_001156685.1:n.1082-34dup
NM_022965.3:c.931-528dup	NP_075254.1:n.931-528dup
XM_006713868.1:c.1082-34dup	XP_006713931.1:n.1082-34dup
XM_006713869.1:c.1082-34dup	XP_006713932.1:n.1082-34dup
XM_006713870.1:c.1082-34dup	XP_006713933.1:n.1082-34dup
XM_006713871.1:c.1082-34dup	XP_006713934.1:n.1082-34dup
XM_006713872.1:c.1076-34dup	XP_006713935.1:n.1076-34dup
XM_006713873.1:c.1076-34dup	XP_006713936.1:n.1076-34dup
XM_011513420.1:c.1076-34dup	XP_011511722.1:n.1076-34dup
XM_011513422.1:c.1076-34dup	XP_011511724.1:n.1076-34dup
NM_001354809.1:c.1076-34dup	NP_001341738.1:n.1076-34dup
NM_001354810.1:c.1076-34dup	NP_001341739.1:n.1076-34dup
NR_148971.1:n.1483-34dup
NM_001354809.2:c.1076-34dup	NP_001341738.1:n.1076-34dup
NM_001354810.2:c.1076-34dup	NP_001341739.1:n.1076-34dup
NR_148971.2:n.1502-34dup
NM_000142.5:c.1076-34dup MANE Select	NP_000133.1:n.1076-34dup
NM_001163213.2:c.1082-34dup	NP_001156685.1:n.1082-34dup
NM_022965.4:c.931-528dup	NP_075254.1:n.931-528dup