Canonical Allele Identifier: CA2810247

Gene: FGFR3

Linked Data

• dbSNP Id: rs746028046
• ExAC: 4:1806039 A / ATTG
• gnomAD v2: 4-1806039-A-ATTG
• MyVariant Identifiers: chr4:g.1806039_1806040insTTG (hg19) ; chr4:g.1804312_1804313insTTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1804312_1804313insTTG , CM000666.2:g.1804312_1804313insTTG	GRCh38
NC_000004.11:g.1806039_1806040insTTG , CM000666.1:g.1806039_1806040insTTG	GRCh37
NC_000004.10:g.1775837_1775838insTTG	NCBI36
NG_012632.1:g.16001_16002insTTG , LRG_1021:g.16001_16002insTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340107.9:c.1082-18_1082-17insTTG	ENSP00000339824.4:n.1082-18_1082-17insTTG
ENST00000260795.8:c.*132-18_*132-17insTTG	ENSP00000260795.3:n.*132-18_*132-17insTTG
ENST00000352904.6:c.931-512_931-511insTTG	ENSP00000231803.1:n.931-512_931-511insTTG
ENST00000412135.7:c.1064-18_1064-17insTTG	ENSP00000412903.3:n.1064-18_1064-17insTTG
ENST00000440486.8:c.1076-18_1076-17insTTG MANE Select	ENSP00000414914.2:n.1076-18_1076-17insTTG
ENST00000481110.7:c.1076-18_1076-17insTTG	ENSP00000420533.2:n.1076-18_1076-17insTTG
ENST00000643463.1:n.227-18_227-17insTTG
ENST00000260795.6:c.1076-18_1076-17insTTG	ENSP00000260795.2:n.1076-18_1076-17insTTG
ENST00000340107.8:c.1082-18_1082-17insTTG	ENSP00000339824.4:n.1082-18_1082-17insTTG
ENST00000352904.5:c.931-512_931-511insTTG	ENSP00000231803.1:n.931-512_931-511insTTG
ENST00000412135.6:c.931-512_931-511insTTG	ENSP00000412903.2:n.931-512_931-511insTTG
ENST00000440486.6:c.1076-18_1076-17insTTG	ENSP00000414914.2:n.1076-18_1076-17insTTG
ENST00000481110.6:c.1076-18_1076-17insTTG	ENSP00000420533.2:n.1076-18_1076-17insTTG
ENST00000613647.4:c.*132-18_*132-17insTTG	ENSP00000479472.1:n.*132-18_*132-17insTTG
NM_000142.4:c.1076-18_1076-17insTTG , LRG_1021t1:c.1076-18_1076-17insTTG	NP_000133.1:n.1076-18_1076-17insTTG
NM_001163213.1:c.1082-18_1082-17insTTG , LRG_1021t2:c.1082-18_1082-17insTTG	NP_001156685.1:n.1082-18_1082-17insTTG
NM_022965.3:c.931-512_931-511insTTG	NP_075254.1:n.931-512_931-511insTTG
XM_006713868.1:c.1082-18_1082-17insTTG	XP_006713931.1:n.1082-18_1082-17insTTG
XM_006713869.1:c.1082-18_1082-17insTTG	XP_006713932.1:n.1082-18_1082-17insTTG
XM_006713870.1:c.1082-18_1082-17insTTG	XP_006713933.1:n.1082-18_1082-17insTTG
XM_006713871.1:c.1082-18_1082-17insTTG	XP_006713934.1:n.1082-18_1082-17insTTG
XM_006713872.1:c.1076-18_1076-17insTTG	XP_006713935.1:n.1076-18_1076-17insTTG
XM_006713873.1:c.1076-18_1076-17insTTG	XP_006713936.1:n.1076-18_1076-17insTTG
XM_011513420.1:c.1076-18_1076-17insTTG	XP_011511722.1:n.1076-18_1076-17insTTG
XM_011513422.1:c.1076-18_1076-17insTTG	XP_011511724.1:n.1076-18_1076-17insTTG
NM_001354809.1:c.1076-18_1076-17insTTG	NP_001341738.1:n.1076-18_1076-17insTTG
NM_001354810.1:c.1076-18_1076-17insTTG	NP_001341739.1:n.1076-18_1076-17insTTG
NR_148971.1:n.1483-18_1483-17insTTG
NM_001354809.2:c.1076-18_1076-17insTTG	NP_001341738.1:n.1076-18_1076-17insTTG
NM_001354810.2:c.1076-18_1076-17insTTG	NP_001341739.1:n.1076-18_1076-17insTTG
NR_148971.2:n.1502-18_1502-17insTTG
NM_000142.5:c.1076-18_1076-17insTTG MANE Select	NP_000133.1:n.1076-18_1076-17insTTG
NM_001163213.2:c.1082-18_1082-17insTTG	NP_001156685.1:n.1082-18_1082-17insTTG
NM_022965.4:c.931-512_931-511insTTG	NP_075254.1:n.931-512_931-511insTTG