Canonical Allele Identifier: CA2669553806

Gene: FGFR3

Linked Data

• gnomAD v4: 4-1805215-A-AGGCTGTAGG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1805218_1805226dup , CM000666.2:g.1805218_1805226dup	GRCh38
NC_000004.11:g.1806945_1806953dup , CM000666.1:g.1806945_1806953dup	GRCh37
NC_000004.10:g.1776743_1776751dup	NCBI36
NG_012632.1:g.16907_16915dup , LRG_1021:g.16907_16915dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340107.9:c.1419-137_1419-129dup	ENSP00000339824.4:n.1419-137_1419-129dup
ENST00000260795.8:c.*469-137_*469-129dup	ENSP00000260795.3:n.*469-137_*469-129dup
ENST00000352904.6:c.1077-137_1077-129dup	ENSP00000231803.1:n.1077-137_1077-129dup
ENST00000412135.7:c.1401-137_1401-129dup	ENSP00000412903.3:n.1401-137_1401-129dup
ENST00000440486.8:c.1413-137_1413-129dup MANE Select	ENSP00000414914.2:n.1413-137_1413-129dup
ENST00000481110.7:c.1416-137_1416-129dup	ENSP00000420533.2:n.1416-137_1416-129dup
ENST00000260795.6:c.1413-137_1413-129dup	ENSP00000260795.2:n.1413-137_1413-129dup
ENST00000340107.8:c.1419-137_1419-129dup	ENSP00000339824.4:n.1419-137_1419-129dup
ENST00000352904.5:c.1077-137_1077-129dup	ENSP00000231803.1:n.1077-137_1077-129dup
ENST00000412135.6:c.1077-137_1077-129dup	ENSP00000412903.2:n.1077-137_1077-129dup
ENST00000440486.6:c.1413-137_1413-129dup	ENSP00000414914.2:n.1413-137_1413-129dup
ENST00000469068.1:n.479-137_479-129dup
ENST00000481110.6:c.1416-137_1416-129dup	ENSP00000420533.2:n.1416-137_1416-129dup
ENST00000613647.4:c.*469-137_*469-129dup	ENSP00000479472.1:n.*469-137_*469-129dup
NM_000142.4:c.1413-137_1413-129dup , LRG_1021t1:c.1413-137_1413-129dup	NP_000133.1:n.1413-137_1413-129dup
NM_001163213.1:c.1419-137_1419-129dup , LRG_1021t2:c.1419-137_1419-129dup	NP_001156685.1:n.1419-137_1419-129dup
NM_022965.3:c.1077-137_1077-129dup	NP_075254.1:n.1077-137_1077-129dup
XM_006713868.1:c.1425-137_1425-129dup	XP_006713931.1:n.1425-137_1425-129dup
XM_006713869.1:c.1425-137_1425-129dup	XP_006713932.1:n.1425-137_1425-129dup
XM_006713870.1:c.1422-137_1422-129dup	XP_006713933.1:n.1422-137_1422-129dup
XM_006713871.1:c.1419-137_1419-129dup	XP_006713934.1:n.1419-137_1419-129dup
XM_006713872.1:c.1416-137_1416-129dup	XP_006713935.1:n.1416-137_1416-129dup
XM_006713873.1:c.1413-137_1413-129dup	XP_006713936.1:n.1413-137_1413-129dup
XM_011513420.1:c.1419-137_1419-129dup	XP_011511722.1:n.1419-137_1419-129dup
XM_011513422.1:c.1416-137_1416-129dup	XP_011511724.1:n.1416-137_1416-129dup
NM_001354809.1:c.1416-137_1416-129dup	NP_001341738.1:n.1416-137_1416-129dup
NM_001354810.1:c.1416-137_1416-129dup	NP_001341739.1:n.1416-137_1416-129dup
NR_148971.1:n.1820-137_1820-129dup
NM_001354809.2:c.1416-137_1416-129dup	NP_001341738.1:n.1416-137_1416-129dup
NM_001354810.2:c.1416-137_1416-129dup	NP_001341739.1:n.1416-137_1416-129dup
NR_148971.2:n.1839-137_1839-129dup
NM_000142.5:c.1413-137_1413-129dup MANE Select	NP_000133.1:n.1413-137_1413-129dup
NM_001163213.2:c.1419-137_1419-129dup	NP_001156685.1:n.1419-137_1419-129dup
NM_022965.4:c.1077-137_1077-129dup	NP_075254.1:n.1077-137_1077-129dup