Canonical Allele Identifier: CA791739729

Gene: FGFR3

Linked Data

• dbSNP Id: rs1398059949
• gnomAD v3: 4-1805991-TGCTGGGAGCA-T
• gnomAD v4: 4-1805991-TGCTGGGAGCA-T
• MyVariant Identifiers: chr4:g.1807719_1807728del (hg19) ; chr4:g.1805992_1806001del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1805994_1806003del , CM000666.2:g.1805994_1806003del	GRCh38
NC_000004.11:g.1807721_1807730del , CM000666.1:g.1807721_1807730del	GRCh37
NC_000004.10:g.1777519_1777528del	NCBI36
NG_012632.1:g.17683_17692del , LRG_1021:g.17683_17692del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340107.9:c.1842+54_1843-48del	ENSP00000339824.4:n.1842+54_1843-48del
ENST00000260795.8:c.*892+54_*893-48del	ENSP00000260795.3:n.*892+54_*893-48del
ENST00000352904.6:c.1500+54_1501-48del	ENSP00000231803.1:n.1500+54_1501-48del
ENST00000412135.7:c.1824+54_1825-48del	ENSP00000412903.3:n.1824+54_1825-48del
ENST00000440486.8:c.1836+54_1837-48del MANE Select	ENSP00000414914.2:n.1836+54_1837-48del
ENST00000481110.7:c.1839+54_1840-48del	ENSP00000420533.2:n.1839+54_1840-48del
ENST00000260795.6:c.1836+54_1837-48del	ENSP00000260795.2:n.1836+54_1837-48del
ENST00000340107.8:c.1842+54_1843-48del	ENSP00000339824.4:n.1842+54_1843-48del
ENST00000352904.5:c.1500+54_1501-48del	ENSP00000231803.1:n.1500+54_1501-48del
ENST00000412135.6:c.1500+54_1501-48del	ENSP00000412903.2:n.1500+54_1501-48del
ENST00000440486.6:c.1836+54_1837-48del	ENSP00000414914.2:n.1836+54_1837-48del
ENST00000481110.6:c.1839+54_1840-48del	ENSP00000420533.2:n.1839+54_1840-48del
ENST00000613647.4:c.*892+54_*893-48del	ENSP00000479472.1:n.*892+54_*893-48del
NM_000142.4:c.1836+54_1837-48del , LRG_1021t1:c.1836+54_1837-48del	NP_000133.1:n.1836+54_1837-48del
NM_001163213.1:c.1842+54_1843-48del , LRG_1021t2:c.1842+54_1843-48del	NP_001156685.1:n.1842+54_1843-48del
NM_022965.3:c.1500+54_1501-48del	NP_075254.1:n.1500+54_1501-48del
XM_006713868.1:c.1848+54_1849-48del	XP_006713931.1:n.1848+54_1849-48del
XM_006713869.1:c.1848+54_1849-48del	XP_006713932.1:n.1848+54_1849-48del
XM_006713870.1:c.1845+54_1846-48del	XP_006713933.1:n.1845+54_1846-48del
XM_006713871.1:c.1842+54_1843-48del	XP_006713934.1:n.1842+54_1843-48del
XM_006713872.1:c.1839+54_1840-48del	XP_006713935.1:n.1839+54_1840-48del
XM_006713873.1:c.1836+54_1837-48del	XP_006713936.1:n.1836+54_1837-48del
XM_011513420.1:c.1842+54_1843-48del	XP_011511722.1:n.1842+54_1843-48del
XM_011513422.1:c.1839+54_1840-48del	XP_011511724.1:n.1839+54_1840-48del
NM_001354809.1:c.1839+54_1840-48del	NP_001341738.1:n.1839+54_1840-48del
NM_001354810.1:c.1839+54_1840-48del	NP_001341739.1:n.1839+54_1840-48del
NR_148971.1:n.2243+54_2244-48del
NM_001354809.2:c.1839+54_1840-48del	NP_001341738.1:n.1839+54_1840-48del
NM_001354810.2:c.1839+54_1840-48del	NP_001341739.1:n.1839+54_1840-48del
NR_148971.2:n.2262+54_2263-48del
NM_000142.5:c.1836+54_1837-48del MANE Select	NP_000133.1:n.1836+54_1837-48del
NM_001163213.2:c.1842+54_1843-48del	NP_001156685.1:n.1842+54_1843-48del
NM_022965.4:c.1500+54_1501-48del	NP_075254.1:n.1500+54_1501-48del