Canonical Allele Identifier: CA549175901

Gene: FGFR3

Linked Data

• dbSNP Id: rs1560431129
• gnomAD v2: 4-1806126-GCTT-G
• gnomAD v4: 4-1804399-GCTT-G
• MyVariant Identifiers: chr4:g.1806127_1806129del (hg19) ; chr4:g.1804400_1804402del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1804404_1804406del , CM000666.2:g.1804404_1804406del	GRCh38
NC_000004.11:g.1806131_1806133del , CM000666.1:g.1806131_1806133del	GRCh37
NC_000004.10:g.1775929_1775931del	NCBI36
NG_012632.1:g.16093_16095del , LRG_1021:g.16093_16095del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340107.9:c.1156_1158del	ENSP00000339824.4:p.Phe386del
ENST00000260795.8:c.*206_*208del	ENSP00000260795.3:n.*206_*208del
ENST00000352904.6:c.931-420_931-418del	ENSP00000231803.1:n.931-420_931-418del
ENST00000412135.7:c.1138_1140del	ENSP00000412903.3:p.Phe380del
ENST00000440486.8:c.1150_1152del MANE Select	ENSP00000414914.2:p.Phe384del
ENST00000481110.7:c.1150_1152del	ENSP00000420533.2:p.Phe384del
ENST00000643463.1:n.301_303del
ENST00000260795.6:c.1150_1152del	ENSP00000260795.2:p.Phe384del
ENST00000340107.8:c.1156_1158del	ENSP00000339824.4:p.Phe386del
ENST00000352904.5:c.931-420_931-418del	ENSP00000231803.1:n.931-420_931-418del
ENST00000412135.6:c.931-420_931-418del	ENSP00000412903.2:n.931-420_931-418del
ENST00000440486.6:c.1150_1152del	ENSP00000414914.2:p.Phe384del
ENST00000481110.6:c.1150_1152del	ENSP00000420533.2:p.Phe384del
ENST00000613647.4:c.*206_*208del	ENSP00000479472.1:n.*206_*208del
NM_000142.4:c.1150_1152del , LRG_1021t1:c.1150_1152del	NP_000133.1:p.Phe384del
NM_001163213.1:c.1156_1158del , LRG_1021t2:c.1156_1158del	NP_001156685.1:p.Phe386del
NM_022965.3:c.931-420_931-418del	NP_075254.1:n.931-420_931-418del
XM_006713868.1:c.1156_1158del	XP_006713931.1:p.Phe386del
XM_006713869.1:c.1156_1158del	XP_006713932.1:p.Phe386del
XM_006713870.1:c.1156_1158del	XP_006713933.1:p.Phe386del
XM_006713871.1:c.1156_1158del	XP_006713934.1:p.Phe386del
XM_006713872.1:c.1150_1152del	XP_006713935.1:p.Phe384del
XM_006713873.1:c.1150_1152del	XP_006713936.1:p.Phe384del
XM_011513420.1:c.1150_1152del	XP_011511722.1:p.Phe384del
XM_011513422.1:c.1150_1152del	XP_011511724.1:p.Phe384del
NM_001354809.1:c.1150_1152del	NP_001341738.1:p.Phe384del
NM_001354810.1:c.1150_1152del	NP_001341739.1:p.Phe384del
NR_148971.1:n.1557_1559del
NM_001354809.2:c.1150_1152del	NP_001341738.1:p.Phe384del
NM_001354810.2:c.1150_1152del	NP_001341739.1:p.Phe384del
NR_148971.2:n.1576_1578del
NM_000142.5:c.1150_1152del MANE Select	NP_000133.1:p.Phe384del
NM_001163213.2:c.1156_1158del	NP_001156685.1:p.Phe386del
NM_022965.4:c.931-420_931-418del	NP_075254.1:n.931-420_931-418del