Canonical Allele Identifier: CA1433506307

Gene: FGFR3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1803744A= , CM000666.2:g.1803744A=	GRCh38
NC_000004.11:g.1805471A= , CM000666.1:g.1805471A=	GRCh37
NC_000004.10:g.1775269A=	NCBI36
NG_012632.1:g.15433A= , LRG_1021:g.15433A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340107.9:c.1082-586A=	ENSP00000339824.4:n.1082-586A=
ENST00000260795.8:c.*39A=	ENSP00000260795.3:n.*39A=
ENST00000352904.6:c.931-1080A=	ENSP00000231803.1:n.931-1080A=
ENST00000412135.7:c.971A=	ENSP00000412903.3:p.Asn324=
ENST00000440486.8:c.983A= MANE Select	ENSP00000414914.2:p.Asn328=
ENST00000481110.7:c.983A=	ENSP00000420533.2:p.Asn328=
ENST00000643463.1:n.227-586A=
ENST00000260795.6:c.983A=	ENSP00000260795.2:p.Asn328=
ENST00000340107.8:c.1082-586A=	ENSP00000339824.4:n.1082-586A=
ENST00000352904.5:c.931-1080A=	ENSP00000231803.1:n.931-1080A=
ENST00000412135.6:c.931-1080A=	ENSP00000412903.2:n.931-1080A=
ENST00000440486.6:c.983A=	ENSP00000414914.2:p.Asn328=
ENST00000481110.6:c.983A=	ENSP00000420533.2:p.Asn328=
ENST00000613647.4:c.*39A=	ENSP00000479472.1:n.*39A=
NM_000142.4:c.983A= , LRG_1021t1:c.983A=	NP_000133.1:p.Asn328=
NM_001163213.1:c.1082-586A= , LRG_1021t2:c.1082-586A=	NP_001156685.1:n.1082-586A=
NM_022965.3:c.931-1080A=	NP_075254.1:n.931-1080A=
XM_006713868.1:c.1082-586A=	XP_006713931.1:n.1082-586A=
XM_006713869.1:c.1082-586A=	XP_006713932.1:n.1082-586A=
XM_006713870.1:c.1082-586A=	XP_006713933.1:n.1082-586A=
XM_006713871.1:c.1082-586A=	XP_006713934.1:n.1082-586A=
XM_006713872.1:c.983A=	XP_006713935.1:p.Asn328=
XM_006713873.1:c.983A=	XP_006713936.1:p.Asn328=
XM_011513420.1:c.983A=	XP_011511722.1:p.Asn328=
XM_011513422.1:c.983A=	XP_011511724.1:p.Asn328=
NM_001354809.1:c.983A=	NP_001341738.1:p.Asn328=
NM_001354810.1:c.983A=	NP_001341739.1:p.Asn328=
NR_148971.1:n.1390A=
NM_001354809.2:c.983A=	NP_001341738.1:p.Asn328=
NM_001354810.2:c.983A=	NP_001341739.1:p.Asn328=
NR_148971.2:n.1409A=
NM_000142.5:c.983A= MANE Select	NP_000133.1:p.Asn328=
NM_001163213.2:c.1082-586A=	NP_001156685.1:n.1082-586A=
NM_022965.4:c.931-1080A=	NP_075254.1:n.931-1080A=