Canonical Allele Identifier: CA1058523018

Gene: FGFR3

Linked Data

• dbSNP Id: rs1720462018
• gnomAD v3: 4-1795958-ACCCACCC-A
• gnomAD v4: 4-1795958-ACCCACCC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1795963_1795969del , CM000666.2:g.1795963_1795969del	GRCh38
NC_000004.11:g.1797690_1797696del , CM000666.1:g.1797690_1797696del	GRCh37
NC_000004.10:g.1767488_1767494del	NCBI36
NG_012632.1:g.7652_7658del , LRG_1021:g.7652_7658del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340107.9:c.109+1920_109+1926del	ENSP00000339824.4:n.109+1920_109+1926del
ENST00000260795.8:c.109+1920_109+1926del	ENSP00000260795.3:n.109+1920_109+1926del
ENST00000352904.6:c.109+1920_109+1926del	ENSP00000231803.1:n.109+1920_109+1926del
ENST00000412135.7:c.109+1920_109+1926del	ENSP00000412903.3:n.109+1920_109+1926del
ENST00000440486.8:c.109+1920_109+1926del MANE Select	ENSP00000414914.2:n.109+1920_109+1926del
ENST00000481110.7:c.109+1920_109+1926del	ENSP00000420533.2:n.109+1920_109+1926del
ENST00000260795.6:c.109+1920_109+1926del	ENSP00000260795.2:n.109+1920_109+1926del
ENST00000340107.8:c.109+1920_109+1926del	ENSP00000339824.4:n.109+1920_109+1926del
ENST00000352904.5:c.109+1920_109+1926del	ENSP00000231803.1:n.109+1920_109+1926del
ENST00000412135.6:c.109+1920_109+1926del	ENSP00000412903.2:n.109+1920_109+1926del
ENST00000440486.6:c.109+1920_109+1926del	ENSP00000414914.2:n.109+1920_109+1926del
ENST00000481110.6:c.109+1920_109+1926del	ENSP00000420533.2:n.109+1920_109+1926del
ENST00000613647.4:c.109+1920_109+1926del	ENSP00000479472.1:n.109+1920_109+1926del
NM_000142.4:c.109+1920_109+1926del , LRG_1021t1:c.109+1920_109+1926del	NP_000133.1:n.109+1920_109+1926del
NM_001163213.1:c.109+1920_109+1926del , LRG_1021t2:c.109+1920_109+1926del	NP_001156685.1:n.109+1920_109+1926del
NM_022965.3:c.109+1920_109+1926del	NP_075254.1:n.109+1920_109+1926del
XM_006713868.1:c.109+1920_109+1926del	XP_006713931.1:n.109+1920_109+1926del
XM_006713869.1:c.109+1920_109+1926del	XP_006713932.1:n.109+1920_109+1926del
XM_006713870.1:c.109+1920_109+1926del	XP_006713933.1:n.109+1920_109+1926del
XM_006713871.1:c.109+1920_109+1926del	XP_006713934.1:n.109+1920_109+1926del
XM_006713872.1:c.109+1920_109+1926del	XP_006713935.1:n.109+1920_109+1926del
XM_006713873.1:c.109+1920_109+1926del	XP_006713936.1:n.109+1920_109+1926del
XM_011513420.1:c.109+1920_109+1926del	XP_011511722.1:n.109+1920_109+1926del
XM_011513422.1:c.109+1920_109+1926del	XP_011511724.1:n.109+1920_109+1926del
NM_001354809.1:c.109+1920_109+1926del	NP_001341738.1:n.109+1920_109+1926del
NM_001354810.1:c.109+1920_109+1926del	NP_001341739.1:n.109+1920_109+1926del
NR_148971.1:n.365+1920_365+1926del
NM_001354809.2:c.109+1920_109+1926del	NP_001341738.1:n.109+1920_109+1926del
NM_001354810.2:c.109+1920_109+1926del	NP_001341739.1:n.109+1920_109+1926del
NR_148971.2:n.384+1920_384+1926del
NM_000142.5:c.109+1920_109+1926del MANE Select	NP_000133.1:n.109+1920_109+1926del
NM_001163213.2:c.109+1920_109+1926del	NP_001156685.1:n.109+1920_109+1926del
NM_022965.4:c.109+1920_109+1926del	NP_075254.1:n.109+1920_109+1926del