Canonical Allele Identifier: CA1433507373

Gene: FGFR3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1805397G= , CM000666.2:g.1805397G=	GRCh38
NC_000004.11:g.1807124G= , CM000666.1:g.1807124G=	GRCh37
NC_000004.10:g.1776922G=	NCBI36
NG_012632.1:g.17086G= , LRG_1021:g.17086G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340107.9:c.1461G=	ENSP00000339824.4:p.Gln487=
ENST00000260795.8:c.*511G=	ENSP00000260795.3:n.*511G=
ENST00000352904.6:c.1119G=	ENSP00000231803.1:p.Gln373=
ENST00000412135.7:c.1443G=	ENSP00000412903.3:p.Gln481=
ENST00000440486.8:c.1455G= MANE Select	ENSP00000414914.2:p.Gln485=
ENST00000481110.7:c.1458G=	ENSP00000420533.2:p.Gln486=
ENST00000260795.6:c.1455G=	ENSP00000260795.2:p.Gln485=
ENST00000340107.8:c.1461G=	ENSP00000339824.4:p.Gln487=
ENST00000352904.5:c.1119G=	ENSP00000231803.1:p.Gln373=
ENST00000412135.6:c.1119G=	ENSP00000412903.2:p.Gln373=
ENST00000440486.6:c.1455G=	ENSP00000414914.2:p.Gln485=
ENST00000469068.1:n.521G=
ENST00000481110.6:c.1458G=	ENSP00000420533.2:p.Gln486=
ENST00000613647.4:c.*511G=	ENSP00000479472.1:n.*511G=
NM_000142.4:c.1455G= , LRG_1021t1:c.1455G=	NP_000133.1:p.Gln485=
NM_001163213.1:c.1461G= , LRG_1021t2:c.1461G=	NP_001156685.1:p.Gln487=
NM_022965.3:c.1119G=	NP_075254.1:p.Gln373=
XM_006713868.1:c.1467G=	XP_006713931.1:p.Gln489=
XM_006713869.1:c.1467G=	XP_006713932.1:p.Gln489=
XM_006713870.1:c.1464G=	XP_006713933.1:p.Gln488=
XM_006713871.1:c.1461G=	XP_006713934.1:p.Gln487=
XM_006713872.1:c.1458G=	XP_006713935.1:p.Gln486=
XM_006713873.1:c.1455G=	XP_006713936.1:p.Gln485=
XM_011513420.1:c.1461G=	XP_011511722.1:p.Gln487=
XM_011513422.1:c.1458G=	XP_011511724.1:p.Gln486=
NM_001354809.1:c.1458G=	NP_001341738.1:p.Gln486=
NM_001354810.1:c.1458G=	NP_001341739.1:p.Gln486=
NR_148971.1:n.1862G=
NM_001354809.2:c.1458G=	NP_001341738.1:p.Gln486=
NM_001354810.2:c.1458G=	NP_001341739.1:p.Gln486=
NR_148971.2:n.1881G=
NM_000142.5:c.1455G= MANE Select	NP_000133.1:p.Gln485=
NM_001163213.2:c.1461G=	NP_001156685.1:p.Gln487=
NM_022965.4:c.1119G=	NP_075254.1:p.Gln373=