Canonical Allele Identifier: CA2669553879

Gene: FGFR3

Linked Data

• gnomAD v4: 4-1805288-TGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1805291_1805292del , CM000666.2:g.1805291_1805292del	GRCh38
NC_000004.11:g.1807018_1807019del , CM000666.1:g.1807018_1807019del	GRCh37
NC_000004.10:g.1776816_1776817del	NCBI36
NG_012632.1:g.16980_16981del , LRG_1021:g.16980_16981del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340107.9:c.1419-64_1419-63del	ENSP00000339824.4:n.1419-64_1419-63del
ENST00000260795.8:c.*469-64_*469-63del	ENSP00000260795.3:n.*469-64_*469-63del
ENST00000352904.6:c.1077-64_1077-63del	ENSP00000231803.1:n.1077-64_1077-63del
ENST00000412135.7:c.1401-64_1401-63del	ENSP00000412903.3:n.1401-64_1401-63del
ENST00000440486.8:c.1413-64_1413-63del MANE Select	ENSP00000414914.2:n.1413-64_1413-63del
ENST00000481110.7:c.1416-64_1416-63del	ENSP00000420533.2:n.1416-64_1416-63del
ENST00000260795.6:c.1413-64_1413-63del	ENSP00000260795.2:n.1413-64_1413-63del
ENST00000340107.8:c.1419-64_1419-63del	ENSP00000339824.4:n.1419-64_1419-63del
ENST00000352904.5:c.1077-64_1077-63del	ENSP00000231803.1:n.1077-64_1077-63del
ENST00000412135.6:c.1077-64_1077-63del	ENSP00000412903.2:n.1077-64_1077-63del
ENST00000440486.6:c.1413-64_1413-63del	ENSP00000414914.2:n.1413-64_1413-63del
ENST00000469068.1:n.479-64_479-63del
ENST00000481110.6:c.1416-64_1416-63del	ENSP00000420533.2:n.1416-64_1416-63del
ENST00000613647.4:c.*469-64_*469-63del	ENSP00000479472.1:n.*469-64_*469-63del
NM_000142.4:c.1413-64_1413-63del , LRG_1021t1:c.1413-64_1413-63del	NP_000133.1:n.1413-64_1413-63del
NM_001163213.1:c.1419-64_1419-63del , LRG_1021t2:c.1419-64_1419-63del	NP_001156685.1:n.1419-64_1419-63del
NM_022965.3:c.1077-64_1077-63del	NP_075254.1:n.1077-64_1077-63del
XM_006713868.1:c.1425-64_1425-63del	XP_006713931.1:n.1425-64_1425-63del
XM_006713869.1:c.1425-64_1425-63del	XP_006713932.1:n.1425-64_1425-63del
XM_006713870.1:c.1422-64_1422-63del	XP_006713933.1:n.1422-64_1422-63del
XM_006713871.1:c.1419-64_1419-63del	XP_006713934.1:n.1419-64_1419-63del
XM_006713872.1:c.1416-64_1416-63del	XP_006713935.1:n.1416-64_1416-63del
XM_006713873.1:c.1413-64_1413-63del	XP_006713936.1:n.1413-64_1413-63del
XM_011513420.1:c.1419-64_1419-63del	XP_011511722.1:n.1419-64_1419-63del
XM_011513422.1:c.1416-64_1416-63del	XP_011511724.1:n.1416-64_1416-63del
NM_001354809.1:c.1416-64_1416-63del	NP_001341738.1:n.1416-64_1416-63del
NM_001354810.1:c.1416-64_1416-63del	NP_001341739.1:n.1416-64_1416-63del
NR_148971.1:n.1820-64_1820-63del
NM_001354809.2:c.1416-64_1416-63del	NP_001341738.1:n.1416-64_1416-63del
NM_001354810.2:c.1416-64_1416-63del	NP_001341739.1:n.1416-64_1416-63del
NR_148971.2:n.1839-64_1839-63del
NM_000142.5:c.1413-64_1413-63del MANE Select	NP_000133.1:n.1413-64_1413-63del
NM_001163213.2:c.1419-64_1419-63del	NP_001156685.1:n.1419-64_1419-63del
NM_022965.4:c.1077-64_1077-63del	NP_075254.1:n.1077-64_1077-63del