Canonical Allele Identifier: CA355978035

Gene: FGFR3

Linked Data

• ClinVar Variation Id: 1698186
• ClinVar RCV Id: RCV002269609
• dbSNP Id: rs1560426864
• gnomAD v3: 4-1803699-G-A
• gnomAD v4: 4-1803699-G-A
• MyVariant Identifiers: chr4:g.1805426G>A (hg19) ; chr4:g.1803699G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1803699G>A , CM000666.2:g.1803699G>A	GRCh38
NC_000004.11:g.1805426G>A , CM000666.1:g.1805426G>A	GRCh37
NC_000004.10:g.1775224G>A	NCBI36
NG_012632.1:g.15388G>A , LRG_1021:g.15388G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340107.9:c.1082-631G>A	ENSP00000339824.4:n.1082-631G>A
ENST00000260795.8:c.1089G>A	ENSP00000260795.3:p.Gly363=
ENST00000352904.6:c.931-1125G>A	ENSP00000231803.1:n.931-1125G>A
ENST00000412135.7:c.926G>A	ENSP00000412903.3:p.Gly309Asp
ENST00000440486.8:c.938G>A MANE Select	ENSP00000414914.2:p.Gly313Asp
ENST00000481110.7:c.938G>A	ENSP00000420533.2:p.Gly313Asp
ENST00000643463.1:n.227-631G>A
ENST00000260795.6:c.938G>A	ENSP00000260795.2:p.Gly313Asp
ENST00000340107.8:c.1082-631G>A	ENSP00000339824.4:n.1082-631G>A
ENST00000352904.5:c.931-1125G>A	ENSP00000231803.1:n.931-1125G>A
ENST00000412135.6:c.931-1125G>A	ENSP00000412903.2:n.931-1125G>A
ENST00000440486.6:c.938G>A	ENSP00000414914.2:p.Gly313Asp
ENST00000481110.6:c.938G>A	ENSP00000420533.2:p.Gly313Asp
ENST00000507588.1:c.296G>A	ENSP00000427289.1:p.Gly99Asp
ENST00000613647.4:c.1089G>A	ENSP00000479472.1:p.Gly363=
NM_000142.4:c.938G>A , LRG_1021t1:c.938G>A	NP_000133.1:p.Gly313Asp
NM_001163213.1:c.1082-631G>A , LRG_1021t2:c.1082-631G>A	NP_001156685.1:n.1082-631G>A
NM_022965.3:c.931-1125G>A	NP_075254.1:n.931-1125G>A
XM_006713868.1:c.1082-631G>A	XP_006713931.1:n.1082-631G>A
XM_006713869.1:c.1082-631G>A	XP_006713932.1:n.1082-631G>A
XM_006713870.1:c.1082-631G>A	XP_006713933.1:n.1082-631G>A
XM_006713871.1:c.1082-631G>A	XP_006713934.1:n.1082-631G>A
XM_006713872.1:c.938G>A	XP_006713935.1:p.Gly313Asp
XM_006713873.1:c.938G>A	XP_006713936.1:p.Gly313Asp
XM_011513420.1:c.938G>A	XP_011511722.1:p.Gly313Asp
XM_011513422.1:c.938G>A	XP_011511724.1:p.Gly313Asp
NM_001354809.1:c.938G>A	NP_001341738.1:p.Gly313Asp
NM_001354810.1:c.938G>A	NP_001341739.1:p.Gly313Asp
NR_148971.1:n.1345G>A
NM_001354809.2:c.938G>A	NP_001341738.1:p.Gly313Asp
NM_001354810.2:c.938G>A	NP_001341739.1:p.Gly313Asp
NR_148971.2:n.1364G>A
NM_000142.5:c.938G>A MANE Select	NP_000133.1:p.Gly313Asp
NM_001163213.2:c.1082-631G>A	NP_001156685.1:n.1082-631G>A
NM_022965.4:c.931-1125G>A	NP_075254.1:n.931-1125G>A