Canonical Allele Identifier: CA2697557052

Gene: FGFR3

Linked Data

• ClinVar Variation Id: 2721671
• ClinVar RCV Id: RCV003556556

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1804389_1804390delinsCG , CM000666.2:g.1804389_1804390delinsCG	GRCh38
NC_000004.11:g.1806116_1806117delinsCG , CM000666.1:g.1806116_1806117delinsCG	GRCh37
NC_000004.10:g.1775914_1775915delinsCG	NCBI36
NG_012632.1:g.16078_16079delinsCG , LRG_1021:g.16078_16079delinsCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000340107.9:c.1141_1142delinsCG	ENSP00000339824.4:p.Tyr381Arg
ENST00000260795.8:c.*191_*192delinsCG	ENSP00000260795.3:n.*191_*192delinsCG
ENST00000352904.6:c.931-435_931-434delinsCG	ENSP00000231803.1:n.931-435_931-434delinsCG
ENST00000412135.7:c.1123_1124delinsCG	ENSP00000412903.3:p.Tyr375Arg
ENST00000440486.8:c.1135_1136delinsCG MANE Select	ENSP00000414914.2:p.Tyr379Arg
ENST00000481110.7:c.1135_1136delinsCG	ENSP00000420533.2:p.Tyr379Arg
ENST00000643463.1:n.286_287delinsCG
ENST00000260795.6:c.1135_1136delinsCG	ENSP00000260795.2:p.Tyr379Arg
ENST00000340107.8:c.1141_1142delinsCG	ENSP00000339824.4:p.Tyr381Arg
ENST00000352904.5:c.931-435_931-434delinsCG	ENSP00000231803.1:n.931-435_931-434delinsCG
ENST00000412135.6:c.931-435_931-434delinsCG	ENSP00000412903.2:n.931-435_931-434delinsCG
ENST00000440486.6:c.1135_1136delinsCG	ENSP00000414914.2:p.Tyr379Arg
ENST00000481110.6:c.1135_1136delinsCG	ENSP00000420533.2:p.Tyr379Arg
ENST00000613647.4:c.*191_*192delinsCG	ENSP00000479472.1:n.*191_*192delinsCG
NM_000142.4:c.1135_1136delinsCG , LRG_1021t1:c.1135_1136delinsCG	NP_000133.1:p.Tyr379Arg
NM_001163213.1:c.1141_1142delinsCG , LRG_1021t2:c.1141_1142delinsCG	NP_001156685.1:p.Tyr381Arg
NM_022965.3:c.931-435_931-434delinsCG	NP_075254.1:n.931-435_931-434delinsCG
XM_006713868.1:c.1141_1142delinsCG	XP_006713931.1:p.Tyr381Arg
XM_006713869.1:c.1141_1142delinsCG	XP_006713932.1:p.Tyr381Arg
XM_006713870.1:c.1141_1142delinsCG	XP_006713933.1:p.Tyr381Arg
XM_006713871.1:c.1141_1142delinsCG	XP_006713934.1:p.Tyr381Arg
XM_006713872.1:c.1135_1136delinsCG	XP_006713935.1:p.Tyr379Arg
XM_006713873.1:c.1135_1136delinsCG	XP_006713936.1:p.Tyr379Arg
XM_011513420.1:c.1135_1136delinsCG	XP_011511722.1:p.Tyr379Arg
XM_011513422.1:c.1135_1136delinsCG	XP_011511724.1:p.Tyr379Arg
NM_001354809.1:c.1135_1136delinsCG	NP_001341738.1:p.Tyr379Arg
NM_001354810.1:c.1135_1136delinsCG	NP_001341739.1:p.Tyr379Arg
NR_148971.1:n.1542_1543delinsCG
NM_001354809.2:c.1135_1136delinsCG	NP_001341738.1:p.Tyr379Arg
NM_001354810.2:c.1135_1136delinsCG	NP_001341739.1:p.Tyr379Arg
NR_148971.2:n.1561_1562delinsCG
NM_000142.5:c.1135_1136delinsCG MANE Select	NP_000133.1:p.Tyr379Arg
NM_001163213.2:c.1141_1142delinsCG	NP_001156685.1:p.Tyr381Arg
NM_022965.4:c.931-435_931-434delinsCG	NP_075254.1:n.931-435_931-434delinsCG