Canonical Allele Identifier: CA2669553159

Gene: FGFR3

Linked Data

• gnomAD v4: 4-1804647-G-GTC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1804651_1804652dup , CM000666.2:g.1804651_1804652dup	GRCh38
NC_000004.11:g.1806378_1806379dup , CM000666.1:g.1806378_1806379dup	GRCh37
NC_000004.10:g.1776176_1776177dup	NCBI36
NG_012632.1:g.16340_16341dup , LRG_1021:g.16340_16341dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340107.9:c.1272+131_1272+132dup	ENSP00000339824.4:n.1272+131_1272+132dup
ENST00000260795.8:c.*322+131_*322+132dup	ENSP00000260795.3:n.*322+131_*322+132dup
ENST00000352904.6:c.931-173_931-172dup	ENSP00000231803.1:n.931-173_931-172dup
ENST00000412135.7:c.1254+131_1254+132dup	ENSP00000412903.3:n.1254+131_1254+132dup
ENST00000440486.8:c.1266+131_1266+132dup MANE Select	ENSP00000414914.2:n.1266+131_1266+132dup
ENST00000481110.7:c.1266+131_1266+132dup	ENSP00000420533.2:n.1266+131_1266+132dup
ENST00000260795.6:c.1266+131_1266+132dup	ENSP00000260795.2:n.1266+131_1266+132dup
ENST00000340107.8:c.1272+131_1272+132dup	ENSP00000339824.4:n.1272+131_1272+132dup
ENST00000352904.5:c.931-173_931-172dup	ENSP00000231803.1:n.931-173_931-172dup
ENST00000412135.6:c.931-173_931-172dup	ENSP00000412903.2:n.931-173_931-172dup
ENST00000440486.6:c.1266+131_1266+132dup	ENSP00000414914.2:n.1266+131_1266+132dup
ENST00000469068.1:n.160_161dup
ENST00000481110.6:c.1266+131_1266+132dup	ENSP00000420533.2:n.1266+131_1266+132dup
ENST00000613647.4:c.*322+131_*322+132dup	ENSP00000479472.1:n.*322+131_*322+132dup
NM_000142.4:c.1266+131_1266+132dup , LRG_1021t1:c.1266+131_1266+132dup	NP_000133.1:n.1266+131_1266+132dup
NM_001163213.1:c.1272+131_1272+132dup , LRG_1021t2:c.1272+131_1272+132dup	NP_001156685.1:n.1272+131_1272+132dup
NM_022965.3:c.931-173_931-172dup	NP_075254.1:n.931-173_931-172dup
XM_006713868.1:c.1278+125_1278+126dup	XP_006713931.1:n.1278+125_1278+126dup
XM_006713869.1:c.1278+125_1278+126dup	XP_006713932.1:n.1278+125_1278+126dup
XM_006713870.1:c.1272+131_1272+132dup	XP_006713933.1:n.1272+131_1272+132dup
XM_006713871.1:c.1272+131_1272+132dup	XP_006713934.1:n.1272+131_1272+132dup
XM_006713872.1:c.1266+131_1266+132dup	XP_006713935.1:n.1266+131_1266+132dup
XM_006713873.1:c.1266+131_1266+132dup	XP_006713936.1:n.1266+131_1266+132dup
XM_011513420.1:c.1272+125_1272+126dup	XP_011511722.1:n.1272+125_1272+126dup
XM_011513422.1:c.1266+131_1266+132dup	XP_011511724.1:n.1266+131_1266+132dup
NM_001354809.1:c.1266+131_1266+132dup	NP_001341738.1:n.1266+131_1266+132dup
NM_001354810.1:c.1266+131_1266+132dup	NP_001341739.1:n.1266+131_1266+132dup
NR_148971.1:n.1673+131_1673+132dup
NM_001354809.2:c.1266+131_1266+132dup	NP_001341738.1:n.1266+131_1266+132dup
NM_001354810.2:c.1266+131_1266+132dup	NP_001341739.1:n.1266+131_1266+132dup
NR_148971.2:n.1692+131_1692+132dup
NM_000142.5:c.1266+131_1266+132dup MANE Select	NP_000133.1:n.1266+131_1266+132dup
NM_001163213.2:c.1272+131_1272+132dup	NP_001156685.1:n.1272+131_1272+132dup
NM_022965.4:c.931-173_931-172dup	NP_075254.1:n.931-173_931-172dup