Canonical Allele Identifier: CA645526890

Gene: FGFR3

Linked Data

• COSMIC: COSM5500995

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1803694_1803695insA , CM000666.2:g.1803694_1803695insA	GRCh38
NC_000004.11:g.1805421_1805422insA , CM000666.1:g.1805421_1805422insA	GRCh37
NC_000004.10:g.1775219_1775220insA	NCBI36
NG_012632.1:g.15383_15384insA , LRG_1021:g.15383_15384insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340107.9:c.1081+630_1081+631insA	ENSP00000339824.4:n.1081+630_1081+631insA
ENST00000260795.8:c.1084_1085insA	ENSP00000260795.3:p.Gly362GlufsTer11
ENST00000352904.6:c.931-1130_931-1129insA	ENSP00000231803.1:n.931-1130_931-1129insA
ENST00000412135.7:c.921_922insA	ENSP00000412903.3:p.Ala308SerfsTer4
ENST00000440486.8:c.933_934insA MANE Select	ENSP00000414914.2:p.Ala312SerfsTer4
ENST00000481110.7:c.933_934insA	ENSP00000420533.2:p.Ala312SerfsTer4
ENST00000643463.1:n.226+630_226+631insA
ENST00000260795.6:c.933_934insA	ENSP00000260795.2:p.Ala312SerfsTer4
ENST00000340107.8:c.1081+630_1081+631insA	ENSP00000339824.4:n.1081+630_1081+631insA
ENST00000352904.5:c.931-1130_931-1129insA	ENSP00000231803.1:n.931-1130_931-1129insA
ENST00000412135.6:c.931-1130_931-1129insA	ENSP00000412903.2:n.931-1130_931-1129insA
ENST00000440486.6:c.933_934insA	ENSP00000414914.2:p.Ala312SerfsTer4
ENST00000481110.6:c.933_934insA	ENSP00000420533.2:p.Ala312SerfsTer4
ENST00000507588.1:c.291_292insA	ENSP00000427289.1:p.Ala98SerfsTer4
ENST00000613647.4:c.1084_1085insA	ENSP00000479472.1:p.Gly362GlufsTer11
NM_000142.4:c.933_934insA , LRG_1021t1:c.933_934insA	NP_000133.1:p.Ala312SerfsTer4
NM_001163213.1:c.1081+630_1081+631insA , LRG_1021t2:c.1081+630_1081+631insA	NP_001156685.1:n.1081+630_1081+631insA
NM_022965.3:c.931-1130_931-1129insA	NP_075254.1:n.931-1130_931-1129insA
XM_006713868.1:c.1081+630_1081+631insA	XP_006713931.1:n.1081+630_1081+631insA
XM_006713869.1:c.1081+630_1081+631insA	XP_006713932.1:n.1081+630_1081+631insA
XM_006713870.1:c.1081+630_1081+631insA	XP_006713933.1:n.1081+630_1081+631insA
XM_006713871.1:c.1081+630_1081+631insA	XP_006713934.1:n.1081+630_1081+631insA
XM_006713872.1:c.933_934insA	XP_006713935.1:p.Ala312SerfsTer4
XM_006713873.1:c.933_934insA	XP_006713936.1:p.Ala312SerfsTer4
XM_011513420.1:c.933_934insA	XP_011511722.1:p.Ala312SerfsTer4
XM_011513422.1:c.933_934insA	XP_011511724.1:p.Ala312SerfsTer4
NM_001354809.1:c.933_934insA	NP_001341738.1:p.Ala312SerfsTer4
NM_001354810.1:c.933_934insA	NP_001341739.1:p.Ala312SerfsTer4
NR_148971.1:n.1340_1341insA
NM_001354809.2:c.933_934insA	NP_001341738.1:p.Ala312SerfsTer4
NM_001354810.2:c.933_934insA	NP_001341739.1:p.Ala312SerfsTer4
NR_148971.2:n.1359_1360insA
NM_000142.5:c.933_934insA MANE Select	NP_000133.1:p.Ala312SerfsTer4
NM_001163213.2:c.1081+630_1081+631insA	NP_001156685.1:n.1081+630_1081+631insA
NM_022965.4:c.931-1130_931-1129insA	NP_075254.1:n.931-1130_931-1129insA