Canonical Allele Identifier: CA355987995

Gene: FGFR3

Linked Data - Expert Curation

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1807261G>C , CM000666.2:g.1807261G>C	GRCh38
NC_000004.11:g.1808988G>C , CM000666.1:g.1808988G>C	GRCh37
NC_000004.10:g.1778786G>C	NCBI36
NG_012632.1:g.18950G>C , LRG_1021:g.18950G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340107.9:c.2426G>C	ENSP00000339824.4:p.Ter809Ser
ENST00000260795.8:c.*1476G>C	ENSP00000260795.3:n.*1476G>C
ENST00000352904.6:c.2084G>C	ENSP00000231803.1:p.Ter695Ser
ENST00000412135.7:c.2408G>C	ENSP00000412903.3:p.Ter803Ser
ENST00000440486.8:c.2420G>C MANE Select	ENSP00000414914.2:p.Ter807Ser
ENST00000481110.7:c.2352G>C	ENSP00000420533.2:p.Val784=
ENST00000260795.6:c.2420G>C	ENSP00000260795.2:p.Ter807Ser
ENST00000340107.8:c.2426G>C	ENSP00000339824.4:p.Ter809Ser
ENST00000352904.5:c.2084G>C	ENSP00000231803.1:p.Ter695Ser
ENST00000412135.6:c.2084G>C	ENSP00000412903.2:p.Ter695Ser
ENST00000440486.6:c.2420G>C	ENSP00000414914.2:p.Ter807Ser
ENST00000481110.6:c.2352G>C	ENSP00000420533.2:p.Val784=
ENST00000613647.4:c.*1476G>C	ENSP00000479472.1:n.*1476G>C
NM_000142.4:c.2420G>C , LRG_1021t1:c.2420G>C	NP_000133.1:p.Ter807Ser
NM_001163213.1:c.2426G>C , LRG_1021t2:c.2426G>C	NP_001156685.1:p.Ter809Ser
NM_022965.3:c.2084G>C	NP_075254.1:p.Ter695Ser
XM_006713868.1:c.2435G>C	XP_006713931.1:p.Ter812Ser
XM_006713869.1:c.2432G>C	XP_006713932.1:p.Ter811Ser
XM_006713870.1:c.2432G>C	XP_006713933.1:p.Ter811Ser
XM_006713871.1:c.2429G>C	XP_006713934.1:p.Ter810Ser
XM_006713872.1:c.2423G>C	XP_006713935.1:p.Ter808Ser
XM_006713873.1:c.2423G>C	XP_006713936.1:p.Ter808Ser
XM_011513420.1:c.2429G>C	XP_011511722.1:p.Ter810Ser
XM_011513422.1:c.2426G>C	XP_011511724.1:p.Ter809Ser
NM_001354809.1:c.2423G>C	NP_001341738.1:p.Ter808Ser
NM_001354810.1:c.2352G>C	NP_001341739.1:p.Val784=
NR_148971.1:n.2827G>C
NM_001354809.2:c.2423G>C	NP_001341738.1:p.Ter808Ser
NM_001354810.2:c.2352G>C	NP_001341739.1:p.Val784=
NR_148971.2:n.2846G>C
NM_000142.5:c.2420G>C MANE Select	NP_000133.1:p.Ter807Ser
NM_001163213.2:c.2426G>C	NP_001156685.1:p.Ter809Ser
NM_022965.4:c.2084G>C	NP_075254.1:p.Ter695Ser