Canonical Allele Identifier: CA2669563780

Gene: FGFR3

Linked Data

• gnomAD v4: 4-1803677-GCTCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1803682_1803685del , CM000666.2:g.1803682_1803685del	GRCh38
NC_000004.11:g.1805409_1805412del , CM000666.1:g.1805409_1805412del	GRCh37
NC_000004.10:g.1775207_1775210del	NCBI36
NG_012632.1:g.15371_15374del , LRG_1021:g.15371_15374del

Transcript Alleles

HGVS	Amino-acid change
ENST00000340107.9:c.1081+618_1081+621del	ENSP00000339824.4:n.1081+618_1081+621del
ENST00000260795.8:c.1082-10_1082-7del	ENSP00000260795.3:n.1082-10_1082-7del
ENST00000352904.6:c.931-1142_931-1139del	ENSP00000231803.1:n.931-1142_931-1139del
ENST00000412135.7:c.919-10_919-7del	ENSP00000412903.3:n.919-10_919-7del
ENST00000440486.8:c.931-10_931-7del MANE Select	ENSP00000414914.2:n.931-10_931-7del
ENST00000481110.7:c.931-10_931-7del	ENSP00000420533.2:n.931-10_931-7del
ENST00000643463.1:n.226+618_226+621del
ENST00000260795.6:c.931-10_931-7del	ENSP00000260795.2:n.931-10_931-7del
ENST00000340107.8:c.1081+618_1081+621del	ENSP00000339824.4:n.1081+618_1081+621del
ENST00000352904.5:c.931-1142_931-1139del	ENSP00000231803.1:n.931-1142_931-1139del
ENST00000412135.6:c.931-1142_931-1139del	ENSP00000412903.2:n.931-1142_931-1139del
ENST00000440486.6:c.931-10_931-7del	ENSP00000414914.2:n.931-10_931-7del
ENST00000481110.6:c.931-10_931-7del	ENSP00000420533.2:n.931-10_931-7del
ENST00000507588.1:c.289-10_289-7del	ENSP00000427289.1:n.289-10_289-7del
ENST00000613647.4:c.1082-10_1082-7del	ENSP00000479472.1:n.1082-10_1082-7del
NM_000142.4:c.931-10_931-7del , LRG_1021t1:c.931-10_931-7del	NP_000133.1:n.931-10_931-7del
NM_001163213.1:c.1081+618_1081+621del , LRG_1021t2:c.1081+618_1081+621del	NP_001156685.1:n.1081+618_1081+621del
NM_022965.3:c.931-1142_931-1139del	NP_075254.1:n.931-1142_931-1139del
XM_006713868.1:c.1081+618_1081+621del	XP_006713931.1:n.1081+618_1081+621del
XM_006713869.1:c.1081+618_1081+621del	XP_006713932.1:n.1081+618_1081+621del
XM_006713870.1:c.1081+618_1081+621del	XP_006713933.1:n.1081+618_1081+621del
XM_006713871.1:c.1081+618_1081+621del	XP_006713934.1:n.1081+618_1081+621del
XM_006713872.1:c.931-10_931-7del	XP_006713935.1:n.931-10_931-7del
XM_006713873.1:c.931-10_931-7del	XP_006713936.1:n.931-10_931-7del
XM_011513420.1:c.931-10_931-7del	XP_011511722.1:n.931-10_931-7del
XM_011513422.1:c.931-10_931-7del	XP_011511724.1:n.931-10_931-7del
NM_001354809.1:c.931-10_931-7del	NP_001341738.1:n.931-10_931-7del
NM_001354810.1:c.931-10_931-7del	NP_001341739.1:n.931-10_931-7del
NR_148971.1:n.1338-10_1338-7del
NM_001354809.2:c.931-10_931-7del	NP_001341738.1:n.931-10_931-7del
NM_001354810.2:c.931-10_931-7del	NP_001341739.1:n.931-10_931-7del
NR_148971.2:n.1357-10_1357-7del
NM_000142.5:c.931-10_931-7del MANE Select	NP_000133.1:n.931-10_931-7del
NM_001163213.2:c.1081+618_1081+621del	NP_001156685.1:n.1081+618_1081+621del
NM_022965.4:c.931-1142_931-1139del	NP_075254.1:n.931-1142_931-1139del