Canonical Allele Identifier: CA2578018386

Gene: FGFR3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1805982del , CM000666.2:g.1805982del	GRCh38
NC_000004.11:g.1807709del , CM000666.1:g.1807709del	GRCh37
NC_000004.10:g.1777507del	NCBI36
NG_012632.1:g.17671del , LRG_1021:g.17671del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340107.9:c.1842+42del	ENSP00000339824.4:n.1842+42del
ENST00000260795.8:c.*892+42del	ENSP00000260795.3:n.*892+42del
ENST00000352904.6:c.1500+42del	ENSP00000231803.1:n.1500+42del
ENST00000412135.7:c.1824+42del	ENSP00000412903.3:n.1824+42del
ENST00000440486.8:c.1836+42del MANE Select	ENSP00000414914.2:n.1836+42del
ENST00000481110.7:c.1839+42del	ENSP00000420533.2:n.1839+42del
ENST00000260795.6:c.1836+42del	ENSP00000260795.2:n.1836+42del
ENST00000340107.8:c.1842+42del	ENSP00000339824.4:n.1842+42del
ENST00000352904.5:c.1500+42del	ENSP00000231803.1:n.1500+42del
ENST00000412135.6:c.1500+42del	ENSP00000412903.2:n.1500+42del
ENST00000440486.6:c.1836+42del	ENSP00000414914.2:n.1836+42del
ENST00000481110.6:c.1839+42del	ENSP00000420533.2:n.1839+42del
ENST00000613647.4:c.*892+42del	ENSP00000479472.1:n.*892+42del
NM_000142.4:c.1836+42del , LRG_1021t1:c.1836+42del	NP_000133.1:n.1836+42del
NM_001163213.1:c.1842+42del , LRG_1021t2:c.1842+42del	NP_001156685.1:n.1842+42del
NM_022965.3:c.1500+42del	NP_075254.1:n.1500+42del
XM_006713868.1:c.1848+42del	XP_006713931.1:n.1848+42del
XM_006713869.1:c.1848+42del	XP_006713932.1:n.1848+42del
XM_006713870.1:c.1845+42del	XP_006713933.1:n.1845+42del
XM_006713871.1:c.1842+42del	XP_006713934.1:n.1842+42del
XM_006713872.1:c.1839+42del	XP_006713935.1:n.1839+42del
XM_006713873.1:c.1836+42del	XP_006713936.1:n.1836+42del
XM_011513420.1:c.1842+42del	XP_011511722.1:n.1842+42del
XM_011513422.1:c.1839+42del	XP_011511724.1:n.1839+42del
NM_001354809.1:c.1839+42del	NP_001341738.1:n.1839+42del
NM_001354810.1:c.1839+42del	NP_001341739.1:n.1839+42del
NR_148971.1:n.2243+42del
NM_001354809.2:c.1839+42del	NP_001341738.1:n.1839+42del
NM_001354810.2:c.1839+42del	NP_001341739.1:n.1839+42del
NR_148971.2:n.2262+42del
NM_000142.5:c.1836+42del MANE Select	NP_000133.1:n.1836+42del
NM_001163213.2:c.1842+42del	NP_001156685.1:n.1842+42del
NM_022965.4:c.1500+42del	NP_075254.1:n.1500+42del