Canonical Allele Identifier: CA2578018383

Gene: FGFR3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1805960_1805979del , CM000666.2:g.1805960_1805979del	GRCh38
NC_000004.11:g.1807687_1807706del , CM000666.1:g.1807687_1807706del	GRCh37
NC_000004.10:g.1777485_1777504del	NCBI36
NG_012632.1:g.17649_17668del , LRG_1021:g.17649_17668del

Transcript Alleles

HGVS	Amino-acid change
ENST00000340107.9:c.1842+20_1842+39del	ENSP00000339824.4:n.1842+20_1842+39del
ENST00000260795.8:c.*892+20_*892+39del	ENSP00000260795.3:n.*892+20_*892+39del
ENST00000352904.6:c.1500+20_1500+39del	ENSP00000231803.1:n.1500+20_1500+39del
ENST00000412135.7:c.1824+20_1824+39del	ENSP00000412903.3:n.1824+20_1824+39del
ENST00000440486.8:c.1836+20_1836+39del MANE Select	ENSP00000414914.2:n.1836+20_1836+39del
ENST00000481110.7:c.1839+20_1839+39del	ENSP00000420533.2:n.1839+20_1839+39del
ENST00000260795.6:c.1836+20_1836+39del	ENSP00000260795.2:n.1836+20_1836+39del
ENST00000340107.8:c.1842+20_1842+39del	ENSP00000339824.4:n.1842+20_1842+39del
ENST00000352904.5:c.1500+20_1500+39del	ENSP00000231803.1:n.1500+20_1500+39del
ENST00000412135.6:c.1500+20_1500+39del	ENSP00000412903.2:n.1500+20_1500+39del
ENST00000440486.6:c.1836+20_1836+39del	ENSP00000414914.2:n.1836+20_1836+39del
ENST00000481110.6:c.1839+20_1839+39del	ENSP00000420533.2:n.1839+20_1839+39del
ENST00000613647.4:c.*892+20_*892+39del	ENSP00000479472.1:n.*892+20_*892+39del
NM_000142.4:c.1836+20_1836+39del , LRG_1021t1:c.1836+20_1836+39del	NP_000133.1:n.1836+20_1836+39del
NM_001163213.1:c.1842+20_1842+39del , LRG_1021t2:c.1842+20_1842+39del	NP_001156685.1:n.1842+20_1842+39del
NM_022965.3:c.1500+20_1500+39del	NP_075254.1:n.1500+20_1500+39del
XM_006713868.1:c.1848+20_1848+39del	XP_006713931.1:n.1848+20_1848+39del
XM_006713869.1:c.1848+20_1848+39del	XP_006713932.1:n.1848+20_1848+39del
XM_006713870.1:c.1845+20_1845+39del	XP_006713933.1:n.1845+20_1845+39del
XM_006713871.1:c.1842+20_1842+39del	XP_006713934.1:n.1842+20_1842+39del
XM_006713872.1:c.1839+20_1839+39del	XP_006713935.1:n.1839+20_1839+39del
XM_006713873.1:c.1836+20_1836+39del	XP_006713936.1:n.1836+20_1836+39del
XM_011513420.1:c.1842+20_1842+39del	XP_011511722.1:n.1842+20_1842+39del
XM_011513422.1:c.1839+20_1839+39del	XP_011511724.1:n.1839+20_1839+39del
NM_001354809.1:c.1839+20_1839+39del	NP_001341738.1:n.1839+20_1839+39del
NM_001354810.1:c.1839+20_1839+39del	NP_001341739.1:n.1839+20_1839+39del
NR_148971.1:n.2243+20_2243+39del
NM_001354809.2:c.1839+20_1839+39del	NP_001341738.1:n.1839+20_1839+39del
NM_001354810.2:c.1839+20_1839+39del	NP_001341739.1:n.1839+20_1839+39del
NR_148971.2:n.2262+20_2262+39del
NM_000142.5:c.1836+20_1836+39del MANE Select	NP_000133.1:n.1836+20_1836+39del
NM_001163213.2:c.1842+20_1842+39del	NP_001156685.1:n.1842+20_1842+39del
NM_022965.4:c.1500+20_1500+39del	NP_075254.1:n.1500+20_1500+39del