Canonical Allele Identifier: CA1433507398

Gene: FGFR3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1805449G= , CM000666.2:g.1805449G=	GRCh38
NC_000004.11:g.1807176G= , CM000666.1:g.1807176G=	GRCh37
NC_000004.10:g.1776974G=	NCBI36
NG_012632.1:g.17138G= , LRG_1021:g.17138G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340107.9:c.1513G=	ENSP00000339824.4:p.Val505=
ENST00000260795.8:c.*563G=	ENSP00000260795.3:n.*563G=
ENST00000352904.6:c.1171G=	ENSP00000231803.1:p.Val391=
ENST00000412135.7:c.1495G=	ENSP00000412903.3:p.Val499=
ENST00000440486.8:c.1507G= MANE Select	ENSP00000414914.2:p.Val503=
ENST00000481110.7:c.1510G=	ENSP00000420533.2:p.Val504=
ENST00000260795.6:c.1507G=	ENSP00000260795.2:p.Val503=
ENST00000340107.8:c.1513G=	ENSP00000339824.4:p.Val505=
ENST00000352904.5:c.1171G=	ENSP00000231803.1:p.Val391=
ENST00000412135.6:c.1171G=	ENSP00000412903.2:p.Val391=
ENST00000440486.6:c.1507G=	ENSP00000414914.2:p.Val503=
ENST00000469068.1:n.573G=
ENST00000481110.6:c.1510G=	ENSP00000420533.2:p.Val504=
ENST00000613647.4:c.*563G=	ENSP00000479472.1:n.*563G=
NM_000142.4:c.1507G= , LRG_1021t1:c.1507G=	NP_000133.1:p.Val503=
NM_001163213.1:c.1513G= , LRG_1021t2:c.1513G=	NP_001156685.1:p.Val505=
NM_022965.3:c.1171G=	NP_075254.1:p.Val391=
XM_006713868.1:c.1519G=	XP_006713931.1:p.Val507=
XM_006713869.1:c.1519G=	XP_006713932.1:p.Val507=
XM_006713870.1:c.1516G=	XP_006713933.1:p.Val506=
XM_006713871.1:c.1513G=	XP_006713934.1:p.Val505=
XM_006713872.1:c.1510G=	XP_006713935.1:p.Val504=
XM_006713873.1:c.1507G=	XP_006713936.1:p.Val503=
XM_011513420.1:c.1513G=	XP_011511722.1:p.Val505=
XM_011513422.1:c.1510G=	XP_011511724.1:p.Val504=
NM_001354809.1:c.1510G=	NP_001341738.1:p.Val504=
NM_001354810.1:c.1510G=	NP_001341739.1:p.Val504=
NR_148971.1:n.1914G=
NM_001354809.2:c.1510G=	NP_001341738.1:p.Val504=
NM_001354810.2:c.1510G=	NP_001341739.1:p.Val504=
NR_148971.2:n.1933G=
NM_000142.5:c.1507G= MANE Select	NP_000133.1:p.Val503=
NM_001163213.2:c.1513G=	NP_001156685.1:p.Val505=
NM_022965.4:c.1171G=	NP_075254.1:p.Val391=