Canonical Allele Identifier: CA2810196

Gene: FGFR3

Linked Data

• dbSNP Id: rs775273446
• ExAC: 4:1806010 C / CGT
• gnomAD v2: 4-1806010-C-CGT
• gnomAD v3: 4-1804283-C-CGT
• gnomAD v4: 4-1804283-C-CGT
• MyVariant Identifiers: chr4:g.1806011_1806012insTG (hg19) ; chr4:g.1806010_1806011insGT (hg19) ; chr4:g.1804284_1804285insTG (hg38) ; chr4:g.1804283_1804284insGT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1804285_1804286dup , CM000666.2:g.1804285_1804286dup	GRCh38
NC_000004.11:g.1806012_1806013dup , CM000666.1:g.1806012_1806013dup	GRCh37
NC_000004.10:g.1775810_1775811dup	NCBI36
NG_012632.1:g.15974_15975dup , LRG_1021:g.15974_15975dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340107.9:c.1082-45_1082-44dup	ENSP00000339824.4:n.1082-45_1082-44dup
ENST00000260795.8:c.*132-45_*132-44dup	ENSP00000260795.3:n.*132-45_*132-44dup
ENST00000352904.6:c.931-539_931-538dup	ENSP00000231803.1:n.931-539_931-538dup
ENST00000412135.7:c.1064-45_1064-44dup	ENSP00000412903.3:n.1064-45_1064-44dup
ENST00000440486.8:c.1076-45_1076-44dup MANE Select	ENSP00000414914.2:n.1076-45_1076-44dup
ENST00000481110.7:c.1076-45_1076-44dup	ENSP00000420533.2:n.1076-45_1076-44dup
ENST00000643463.1:n.227-45_227-44dup
ENST00000260795.6:c.1076-45_1076-44dup	ENSP00000260795.2:n.1076-45_1076-44dup
ENST00000340107.8:c.1082-45_1082-44dup	ENSP00000339824.4:n.1082-45_1082-44dup
ENST00000352904.5:c.931-539_931-538dup	ENSP00000231803.1:n.931-539_931-538dup
ENST00000412135.6:c.931-539_931-538dup	ENSP00000412903.2:n.931-539_931-538dup
ENST00000440486.6:c.1076-45_1076-44dup	ENSP00000414914.2:n.1076-45_1076-44dup
ENST00000481110.6:c.1076-45_1076-44dup	ENSP00000420533.2:n.1076-45_1076-44dup
ENST00000613647.4:c.*132-45_*132-44dup	ENSP00000479472.1:n.*132-45_*132-44dup
NM_000142.4:c.1076-45_1076-44dup , LRG_1021t1:c.1076-45_1076-44dup	NP_000133.1:n.1076-45_1076-44dup
NM_001163213.1:c.1082-45_1082-44dup , LRG_1021t2:c.1082-45_1082-44dup	NP_001156685.1:n.1082-45_1082-44dup
NM_022965.3:c.931-539_931-538dup	NP_075254.1:n.931-539_931-538dup
XM_006713868.1:c.1082-45_1082-44dup	XP_006713931.1:n.1082-45_1082-44dup
XM_006713869.1:c.1082-45_1082-44dup	XP_006713932.1:n.1082-45_1082-44dup
XM_006713870.1:c.1082-45_1082-44dup	XP_006713933.1:n.1082-45_1082-44dup
XM_006713871.1:c.1082-45_1082-44dup	XP_006713934.1:n.1082-45_1082-44dup
XM_006713872.1:c.1076-45_1076-44dup	XP_006713935.1:n.1076-45_1076-44dup
XM_006713873.1:c.1076-45_1076-44dup	XP_006713936.1:n.1076-45_1076-44dup
XM_011513420.1:c.1076-45_1076-44dup	XP_011511722.1:n.1076-45_1076-44dup
XM_011513422.1:c.1076-45_1076-44dup	XP_011511724.1:n.1076-45_1076-44dup
NM_001354809.1:c.1076-45_1076-44dup	NP_001341738.1:n.1076-45_1076-44dup
NM_001354810.1:c.1076-45_1076-44dup	NP_001341739.1:n.1076-45_1076-44dup
NR_148971.1:n.1483-45_1483-44dup
NM_001354809.2:c.1076-45_1076-44dup	NP_001341738.1:n.1076-45_1076-44dup
NM_001354810.2:c.1076-45_1076-44dup	NP_001341739.1:n.1076-45_1076-44dup
NR_148971.2:n.1502-45_1502-44dup
NM_000142.5:c.1076-45_1076-44dup MANE Select	NP_000133.1:n.1076-45_1076-44dup
NM_001163213.2:c.1082-45_1082-44dup	NP_001156685.1:n.1082-45_1082-44dup
NM_022965.4:c.931-539_931-538dup	NP_075254.1:n.931-539_931-538dup