Canonical Allele Identifier: CA1433507793

Gene: FGFR3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1806100A= , CM000666.2:g.1806100A=	GRCh38
NC_000004.11:g.1807827A= , CM000666.1:g.1807827A=	GRCh37
NC_000004.10:g.1777625A=	NCBI36
NG_012632.1:g.17789A= , LRG_1021:g.17789A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000340107.9:c.1892A=	ENSP00000339824.4:p.Asn631=
ENST00000260795.8:c.*942A=	ENSP00000260795.3:n.*942A=
ENST00000352904.6:c.1550A=	ENSP00000231803.1:p.Asn517=
ENST00000412135.7:c.1874A=	ENSP00000412903.3:p.Asn625=
ENST00000440486.8:c.1886A= MANE Select	ENSP00000414914.2:p.Asn629=
ENST00000481110.7:c.1889A=	ENSP00000420533.2:p.Asn630=
ENST00000260795.6:c.1886A=	ENSP00000260795.2:p.Asn629=
ENST00000340107.8:c.1892A=	ENSP00000339824.4:p.Asn631=
ENST00000352904.5:c.1550A=	ENSP00000231803.1:p.Asn517=
ENST00000412135.6:c.1550A=	ENSP00000412903.2:p.Asn517=
ENST00000440486.6:c.1886A=	ENSP00000414914.2:p.Asn629=
ENST00000481110.6:c.1889A=	ENSP00000420533.2:p.Asn630=
ENST00000613647.4:c.*942A=	ENSP00000479472.1:n.*942A=
NM_000142.4:c.1886A= , LRG_1021t1:c.1886A=	NP_000133.1:p.Asn629=
NM_001163213.1:c.1892A= , LRG_1021t2:c.1892A=	NP_001156685.1:p.Asn631=
NM_022965.3:c.1550A=	NP_075254.1:p.Asn517=
XM_006713868.1:c.1898A=	XP_006713931.1:p.Asn633=
XM_006713869.1:c.1898A=	XP_006713932.1:p.Asn633=
XM_006713870.1:c.1895A=	XP_006713933.1:p.Asn632=
XM_006713871.1:c.1892A=	XP_006713934.1:p.Asn631=
XM_006713872.1:c.1889A=	XP_006713935.1:p.Asn630=
XM_006713873.1:c.1886A=	XP_006713936.1:p.Asn629=
XM_011513420.1:c.1892A=	XP_011511722.1:p.Asn631=
XM_011513422.1:c.1889A=	XP_011511724.1:p.Asn630=
NM_001354809.1:c.1889A=	NP_001341738.1:p.Asn630=
NM_001354810.1:c.1889A=	NP_001341739.1:p.Asn630=
NR_148971.1:n.2293A=
NM_001354809.2:c.1889A=	NP_001341738.1:p.Asn630=
NM_001354810.2:c.1889A=	NP_001341739.1:p.Asn630=
NR_148971.2:n.2312A=
NM_000142.5:c.1886A= MANE Select	NP_000133.1:p.Asn629=
NM_001163213.2:c.1892A=	NP_001156685.1:p.Asn631=
NM_022965.4:c.1550A=	NP_075254.1:p.Asn517=