Canonical Allele Identifier: CA1433507614

Gene: FGFR3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1805780C= , CM000666.2:g.1805780C=	GRCh38
NC_000004.11:g.1807507C= , CM000666.1:g.1807507C=	GRCh37
NC_000004.10:g.1777305C=	NCBI36
NG_012632.1:g.17469C= , LRG_1021:g.17469C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340107.9:c.1682C=	ENSP00000339824.4:p.Ala561=
ENST00000260795.8:c.*732C=	ENSP00000260795.3:n.*732C=
ENST00000352904.6:c.1340C=	ENSP00000231803.1:p.Ala447=
ENST00000412135.7:c.1664C=	ENSP00000412903.3:p.Ala555=
ENST00000440486.8:c.1676C= MANE Select	ENSP00000414914.2:p.Ala559=
ENST00000481110.7:c.1679C=	ENSP00000420533.2:p.Ala560=
ENST00000260795.6:c.1676C=	ENSP00000260795.2:p.Ala559=
ENST00000340107.8:c.1682C=	ENSP00000339824.4:p.Ala561=
ENST00000352904.5:c.1340C=	ENSP00000231803.1:p.Ala447=
ENST00000412135.6:c.1340C=	ENSP00000412903.2:p.Ala447=
ENST00000440486.6:c.1676C=	ENSP00000414914.2:p.Ala559=
ENST00000469068.1:n.742C=
ENST00000481110.6:c.1679C=	ENSP00000420533.2:p.Ala560=
ENST00000613647.4:c.*732C=	ENSP00000479472.1:n.*732C=
NM_000142.4:c.1676C= , LRG_1021t1:c.1676C=	NP_000133.1:p.Ala559=
NM_001163213.1:c.1682C= , LRG_1021t2:c.1682C=	NP_001156685.1:p.Ala561=
NM_022965.3:c.1340C=	NP_075254.1:p.Ala447=
XM_006713868.1:c.1688C=	XP_006713931.1:p.Ala563=
XM_006713869.1:c.1688C=	XP_006713932.1:p.Ala563=
XM_006713870.1:c.1685C=	XP_006713933.1:p.Ala562=
XM_006713871.1:c.1682C=	XP_006713934.1:p.Ala561=
XM_006713872.1:c.1679C=	XP_006713935.1:p.Ala560=
XM_006713873.1:c.1676C=	XP_006713936.1:p.Ala559=
XM_011513420.1:c.1682C=	XP_011511722.1:p.Ala561=
XM_011513422.1:c.1679C=	XP_011511724.1:p.Ala560=
NM_001354809.1:c.1679C=	NP_001341738.1:p.Ala560=
NM_001354810.1:c.1679C=	NP_001341739.1:p.Ala560=
NR_148971.1:n.2083C=
NM_001354809.2:c.1679C=	NP_001341738.1:p.Ala560=
NM_001354810.2:c.1679C=	NP_001341739.1:p.Ala560=
NR_148971.2:n.2102C=
NM_000142.5:c.1676C= MANE Select	NP_000133.1:p.Ala559=
NM_001163213.2:c.1682C=	NP_001156685.1:p.Ala561=
NM_022965.4:c.1340C=	NP_075254.1:p.Ala447=