Canonical Allele Identifier: CA2669552521

Gene: FGFR3

Linked Data

• gnomAD v4: 4-1804295-G-GGT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1804296_1804297insTG , CM000666.2:g.1804296_1804297insTG	GRCh38
NC_000004.11:g.1806023_1806024insTG , CM000666.1:g.1806023_1806024insTG	GRCh37
NC_000004.10:g.1775821_1775822insTG	NCBI36
NG_012632.1:g.15985_15986insTG , LRG_1021:g.15985_15986insTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000340107.9:c.1082-34_1082-33insTG	ENSP00000339824.4:n.1082-34_1082-33insTG
ENST00000260795.8:c.*132-34_*132-33insTG	ENSP00000260795.3:n.*132-34_*132-33insTG
ENST00000352904.6:c.931-528_931-527insTG	ENSP00000231803.1:n.931-528_931-527insTG
ENST00000412135.7:c.1064-34_1064-33insTG	ENSP00000412903.3:n.1064-34_1064-33insTG
ENST00000440486.8:c.1076-34_1076-33insTG MANE Select	ENSP00000414914.2:n.1076-34_1076-33insTG
ENST00000481110.7:c.1076-34_1076-33insTG	ENSP00000420533.2:n.1076-34_1076-33insTG
ENST00000643463.1:n.227-34_227-33insTG
ENST00000260795.6:c.1076-34_1076-33insTG	ENSP00000260795.2:n.1076-34_1076-33insTG
ENST00000340107.8:c.1082-34_1082-33insTG	ENSP00000339824.4:n.1082-34_1082-33insTG
ENST00000352904.5:c.931-528_931-527insTG	ENSP00000231803.1:n.931-528_931-527insTG
ENST00000412135.6:c.931-528_931-527insTG	ENSP00000412903.2:n.931-528_931-527insTG
ENST00000440486.6:c.1076-34_1076-33insTG	ENSP00000414914.2:n.1076-34_1076-33insTG
ENST00000481110.6:c.1076-34_1076-33insTG	ENSP00000420533.2:n.1076-34_1076-33insTG
ENST00000613647.4:c.*132-34_*132-33insTG	ENSP00000479472.1:n.*132-34_*132-33insTG
NM_000142.4:c.1076-34_1076-33insTG , LRG_1021t1:c.1076-34_1076-33insTG	NP_000133.1:n.1076-34_1076-33insTG
NM_001163213.1:c.1082-34_1082-33insTG , LRG_1021t2:c.1082-34_1082-33insTG	NP_001156685.1:n.1082-34_1082-33insTG
NM_022965.3:c.931-528_931-527insTG	NP_075254.1:n.931-528_931-527insTG
XM_006713868.1:c.1082-34_1082-33insTG	XP_006713931.1:n.1082-34_1082-33insTG
XM_006713869.1:c.1082-34_1082-33insTG	XP_006713932.1:n.1082-34_1082-33insTG
XM_006713870.1:c.1082-34_1082-33insTG	XP_006713933.1:n.1082-34_1082-33insTG
XM_006713871.1:c.1082-34_1082-33insTG	XP_006713934.1:n.1082-34_1082-33insTG
XM_006713872.1:c.1076-34_1076-33insTG	XP_006713935.1:n.1076-34_1076-33insTG
XM_006713873.1:c.1076-34_1076-33insTG	XP_006713936.1:n.1076-34_1076-33insTG
XM_011513420.1:c.1076-34_1076-33insTG	XP_011511722.1:n.1076-34_1076-33insTG
XM_011513422.1:c.1076-34_1076-33insTG	XP_011511724.1:n.1076-34_1076-33insTG
NM_001354809.1:c.1076-34_1076-33insTG	NP_001341738.1:n.1076-34_1076-33insTG
NM_001354810.1:c.1076-34_1076-33insTG	NP_001341739.1:n.1076-34_1076-33insTG
NR_148971.1:n.1483-34_1483-33insTG
NM_001354809.2:c.1076-34_1076-33insTG	NP_001341738.1:n.1076-34_1076-33insTG
NM_001354810.2:c.1076-34_1076-33insTG	NP_001341739.1:n.1076-34_1076-33insTG
NR_148971.2:n.1502-34_1502-33insTG
NM_000142.5:c.1076-34_1076-33insTG MANE Select	NP_000133.1:n.1076-34_1076-33insTG
NM_001163213.2:c.1082-34_1082-33insTG	NP_001156685.1:n.1082-34_1082-33insTG
NM_022965.4:c.931-528_931-527insTG	NP_075254.1:n.931-528_931-527insTG