Canonical Allele Identifier: CA1433507389

Gene: FGFR3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1805437G= , CM000666.2:g.1805437G=	GRCh38
NC_000004.11:g.1807164G= , CM000666.1:g.1807164G=	GRCh37
NC_000004.10:g.1776962G=	NCBI36
NG_012632.1:g.17126G= , LRG_1021:g.17126G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340107.9:c.1501G=	ENSP00000339824.4:p.Ala501=
ENST00000260795.8:c.*551G=	ENSP00000260795.3:n.*551G=
ENST00000352904.6:c.1159G=	ENSP00000231803.1:p.Ala387=
ENST00000412135.7:c.1483G=	ENSP00000412903.3:p.Ala495=
ENST00000440486.8:c.1495G= MANE Select	ENSP00000414914.2:p.Ala499=
ENST00000481110.7:c.1498G=	ENSP00000420533.2:p.Ala500=
ENST00000260795.6:c.1495G=	ENSP00000260795.2:p.Ala499=
ENST00000340107.8:c.1501G=	ENSP00000339824.4:p.Ala501=
ENST00000352904.5:c.1159G=	ENSP00000231803.1:p.Ala387=
ENST00000412135.6:c.1159G=	ENSP00000412903.2:p.Ala387=
ENST00000440486.6:c.1495G=	ENSP00000414914.2:p.Ala499=
ENST00000469068.1:n.561G=
ENST00000481110.6:c.1498G=	ENSP00000420533.2:p.Ala500=
ENST00000613647.4:c.*551G=	ENSP00000479472.1:n.*551G=
NM_000142.4:c.1495G= , LRG_1021t1:c.1495G=	NP_000133.1:p.Ala499=
NM_001163213.1:c.1501G= , LRG_1021t2:c.1501G=	NP_001156685.1:p.Ala501=
NM_022965.3:c.1159G=	NP_075254.1:p.Ala387=
XM_006713868.1:c.1507G=	XP_006713931.1:p.Ala503=
XM_006713869.1:c.1507G=	XP_006713932.1:p.Ala503=
XM_006713870.1:c.1504G=	XP_006713933.1:p.Ala502=
XM_006713871.1:c.1501G=	XP_006713934.1:p.Ala501=
XM_006713872.1:c.1498G=	XP_006713935.1:p.Ala500=
XM_006713873.1:c.1495G=	XP_006713936.1:p.Ala499=
XM_011513420.1:c.1501G=	XP_011511722.1:p.Ala501=
XM_011513422.1:c.1498G=	XP_011511724.1:p.Ala500=
NM_001354809.1:c.1498G=	NP_001341738.1:p.Ala500=
NM_001354810.1:c.1498G=	NP_001341739.1:p.Ala500=
NR_148971.1:n.1902G=
NM_001354809.2:c.1498G=	NP_001341738.1:p.Ala500=
NM_001354810.2:c.1498G=	NP_001341739.1:p.Ala500=
NR_148971.2:n.1921G=
NM_000142.5:c.1495G= MANE Select	NP_000133.1:p.Ala499=
NM_001163213.2:c.1501G=	NP_001156685.1:p.Ala501=
NM_022965.4:c.1159G=	NP_075254.1:p.Ala387=