Canonical Allele Identifier: CA1433507428

Gene: FGFR3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1805493_1805494delinsCA , CM000666.2:g.1805493_1805494delinsCA	GRCh38
NC_000004.11:g.1807220_1807221delinsCA , CM000666.1:g.1807220_1807221delinsCA	GRCh37
NC_000004.10:g.1777018_1777019delinsCA	NCBI36
NG_012632.1:g.17182_17183delinsCA , LRG_1021:g.17182_17183delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340107.9:c.1540+17_1540+18delinsCA	ENSP00000339824.4:n.1540+17_1540+18delinsCA
ENST00000260795.8:c.*590+17_*590+18delinsCA	ENSP00000260795.3:n.*590+17_*590+18delinsCA
ENST00000352904.6:c.1198+17_1198+18delinsCA	ENSP00000231803.1:n.1198+17_1198+18delinsCA
ENST00000412135.7:c.1522+17_1522+18delinsCA	ENSP00000412903.3:n.1522+17_1522+18delinsCA
ENST00000440486.8:c.1534+17_1534+18delinsCA MANE Select	ENSP00000414914.2:n.1534+17_1534+18delinsCA
ENST00000481110.7:c.1537+17_1537+18delinsCA	ENSP00000420533.2:n.1537+17_1537+18delinsCA
ENST00000260795.6:c.1534+17_1534+18delinsCA	ENSP00000260795.2:n.1534+17_1534+18delinsCA
ENST00000340107.8:c.1540+17_1540+18delinsCA	ENSP00000339824.4:n.1540+17_1540+18delinsCA
ENST00000352904.5:c.1198+17_1198+18delinsCA	ENSP00000231803.1:n.1198+17_1198+18delinsCA
ENST00000412135.6:c.1198+17_1198+18delinsCA	ENSP00000412903.2:n.1198+17_1198+18delinsCA
ENST00000440486.6:c.1534+17_1534+18delinsCA	ENSP00000414914.2:n.1534+17_1534+18delinsCA
ENST00000469068.1:n.600+17_600+18delinsCA
ENST00000481110.6:c.1537+17_1537+18delinsCA	ENSP00000420533.2:n.1537+17_1537+18delinsCA
ENST00000613647.4:c.*590+17_*590+18delinsCA	ENSP00000479472.1:n.*590+17_*590+18delinsCA
NM_000142.4:c.1534+17_1534+18delinsCA , LRG_1021t1:c.1534+17_1534+18delinsCA	NP_000133.1:n.1534+17_1534+18delinsCA
NM_001163213.1:c.1540+17_1540+18delinsCA , LRG_1021t2:c.1540+17_1540+18delinsCA	NP_001156685.1:n.1540+17_1540+18delinsCA
NM_022965.3:c.1198+17_1198+18delinsCA	NP_075254.1:n.1198+17_1198+18delinsCA
XM_006713868.1:c.1546+17_1546+18delinsCA	XP_006713931.1:n.1546+17_1546+18delinsCA
XM_006713869.1:c.1546+17_1546+18delinsCA	XP_006713932.1:n.1546+17_1546+18delinsCA
XM_006713870.1:c.1543+17_1543+18delinsCA	XP_006713933.1:n.1543+17_1543+18delinsCA
XM_006713871.1:c.1540+17_1540+18delinsCA	XP_006713934.1:n.1540+17_1540+18delinsCA
XM_006713872.1:c.1537+17_1537+18delinsCA	XP_006713935.1:n.1537+17_1537+18delinsCA
XM_006713873.1:c.1534+17_1534+18delinsCA	XP_006713936.1:n.1534+17_1534+18delinsCA
XM_011513420.1:c.1540+17_1540+18delinsCA	XP_011511722.1:n.1540+17_1540+18delinsCA
XM_011513422.1:c.1537+17_1537+18delinsCA	XP_011511724.1:n.1537+17_1537+18delinsCA
NM_001354809.1:c.1537+17_1537+18delinsCA	NP_001341738.1:n.1537+17_1537+18delinsCA
NM_001354810.1:c.1537+17_1537+18delinsCA	NP_001341739.1:n.1537+17_1537+18delinsCA
NR_148971.1:n.1941+17_1941+18delinsCA
NM_001354809.2:c.1537+17_1537+18delinsCA	NP_001341738.1:n.1537+17_1537+18delinsCA
NM_001354810.2:c.1537+17_1537+18delinsCA	NP_001341739.1:n.1537+17_1537+18delinsCA
NR_148971.2:n.1960+17_1960+18delinsCA
NM_000142.5:c.1534+17_1534+18delinsCA MANE Select	NP_000133.1:n.1534+17_1534+18delinsCA
NM_001163213.2:c.1540+17_1540+18delinsCA	NP_001156685.1:n.1540+17_1540+18delinsCA
NM_022965.4:c.1198+17_1198+18delinsCA	NP_075254.1:n.1198+17_1198+18delinsCA