Canonical Allele Identifier: CA1433507525

Gene: FGFR3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1805644C= , CM000666.2:g.1805644C=	GRCh38
NC_000004.11:g.1807371C= , CM000666.1:g.1807371C=	GRCh37
NC_000004.10:g.1777169C=	NCBI36
NG_012632.1:g.17333C= , LRG_1021:g.17333C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000340107.9:c.1626C=	ENSP00000339824.4:p.Asn542=
ENST00000260795.8:c.*676C=	ENSP00000260795.3:n.*676C=
ENST00000352904.6:c.1284C=	ENSP00000231803.1:p.Asn428=
ENST00000412135.7:c.1608C=	ENSP00000412903.3:p.Asn536=
ENST00000440486.8:c.1620C= MANE Select	ENSP00000414914.2:p.Asn540=
ENST00000481110.7:c.1623C=	ENSP00000420533.2:p.Asn541=
ENST00000260795.6:c.1620C=	ENSP00000260795.2:p.Asn540=
ENST00000340107.8:c.1626C=	ENSP00000339824.4:p.Asn542=
ENST00000352904.5:c.1284C=	ENSP00000231803.1:p.Asn428=
ENST00000412135.6:c.1284C=	ENSP00000412903.2:p.Asn428=
ENST00000440486.6:c.1620C=	ENSP00000414914.2:p.Asn540=
ENST00000469068.1:n.686C=
ENST00000481110.6:c.1623C=	ENSP00000420533.2:p.Asn541=
ENST00000613647.4:c.*676C=	ENSP00000479472.1:n.*676C=
NM_000142.4:c.1620C= , LRG_1021t1:c.1620C=	NP_000133.1:p.Asn540=
NM_001163213.1:c.1626C= , LRG_1021t2:c.1626C=	NP_001156685.1:p.Asn542=
NM_022965.3:c.1284C=	NP_075254.1:p.Asn428=
XM_006713868.1:c.1632C=	XP_006713931.1:p.Asn544=
XM_006713869.1:c.1632C=	XP_006713932.1:p.Asn544=
XM_006713870.1:c.1629C=	XP_006713933.1:p.Asn543=
XM_006713871.1:c.1626C=	XP_006713934.1:p.Asn542=
XM_006713872.1:c.1623C=	XP_006713935.1:p.Asn541=
XM_006713873.1:c.1620C=	XP_006713936.1:p.Asn540=
XM_011513420.1:c.1626C=	XP_011511722.1:p.Asn542=
XM_011513422.1:c.1623C=	XP_011511724.1:p.Asn541=
NM_001354809.1:c.1623C=	NP_001341738.1:p.Asn541=
NM_001354810.1:c.1623C=	NP_001341739.1:p.Asn541=
NR_148971.1:n.2027C=
NM_001354809.2:c.1623C=	NP_001341738.1:p.Asn541=
NM_001354810.2:c.1623C=	NP_001341739.1:p.Asn541=
NR_148971.2:n.2046C=
NM_000142.5:c.1620C= MANE Select	NP_000133.1:p.Asn540=
NM_001163213.2:c.1626C=	NP_001156685.1:p.Asn542=
NM_022965.4:c.1284C=	NP_075254.1:p.Asn428=