Canonical Allele Identifier: CA1433507385

Gene: FGFR3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1805432_1805437delinsACCGGG , CM000666.2:g.1805432_1805437delinsACCGGG	GRCh38
NC_000004.11:g.1807159_1807164delinsACCGGG , CM000666.1:g.1807159_1807164delinsACCGGG	GRCh37
NC_000004.10:g.1776957_1776962delinsACCGGG	NCBI36
NG_012632.1:g.17121_17126delinsACCGGG , LRG_1021:g.17121_17126delinsACCGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340107.9:c.1496_1501delinsACCGGG	ENSP00000339824.4:p.Asp499=
ENST00000260795.8:c.*546_*551delinsACCGGG	ENSP00000260795.3:n.*546_*551delinsACCGGG
ENST00000352904.6:c.1154_1159delinsACCGGG	ENSP00000231803.1:p.Asp385=
ENST00000412135.7:c.1478_1483delinsACCGGG	ENSP00000412903.3:p.Asp493=
ENST00000440486.8:c.1490_1495delinsACCGGG MANE Select	ENSP00000414914.2:p.Asp497=
ENST00000481110.7:c.1493_1498delinsACCGGG	ENSP00000420533.2:p.Asp498=
ENST00000260795.6:c.1490_1495delinsACCGGG	ENSP00000260795.2:p.Asp497=
ENST00000340107.8:c.1496_1501delinsACCGGG	ENSP00000339824.4:p.Asp499=
ENST00000352904.5:c.1154_1159delinsACCGGG	ENSP00000231803.1:p.Asp385=
ENST00000412135.6:c.1154_1159delinsACCGGG	ENSP00000412903.2:p.Asp385=
ENST00000440486.6:c.1490_1495delinsACCGGG	ENSP00000414914.2:p.Asp497=
ENST00000469068.1:n.556_561delinsACCGGG
ENST00000481110.6:c.1493_1498delinsACCGGG	ENSP00000420533.2:p.Asp498=
ENST00000613647.4:c.*546_*551delinsACCGGG	ENSP00000479472.1:n.*546_*551delinsACCGGG
NM_000142.4:c.1490_1495delinsACCGGG , LRG_1021t1:c.1490_1495delinsACCGGG	NP_000133.1:p.Asp497=
NM_001163213.1:c.1496_1501delinsACCGGG , LRG_1021t2:c.1496_1501delinsACCGGG	NP_001156685.1:p.Asp499=
NM_022965.3:c.1154_1159delinsACCGGG	NP_075254.1:p.Asp385=
XM_006713868.1:c.1502_1507delinsACCGGG	XP_006713931.1:p.Asp501=
XM_006713869.1:c.1502_1507delinsACCGGG	XP_006713932.1:p.Asp501=
XM_006713870.1:c.1499_1504delinsACCGGG	XP_006713933.1:p.Asp500=
XM_006713871.1:c.1496_1501delinsACCGGG	XP_006713934.1:p.Asp499=
XM_006713872.1:c.1493_1498delinsACCGGG	XP_006713935.1:p.Asp498=
XM_006713873.1:c.1490_1495delinsACCGGG	XP_006713936.1:p.Asp497=
XM_011513420.1:c.1496_1501delinsACCGGG	XP_011511722.1:p.Asp499=
XM_011513422.1:c.1493_1498delinsACCGGG	XP_011511724.1:p.Asp498=
NM_001354809.1:c.1493_1498delinsACCGGG	NP_001341738.1:p.Asp498=
NM_001354810.1:c.1493_1498delinsACCGGG	NP_001341739.1:p.Asp498=
NR_148971.1:n.1897_1902delinsACCGGG
NM_001354809.2:c.1493_1498delinsACCGGG	NP_001341738.1:p.Asp498=
NM_001354810.2:c.1493_1498delinsACCGGG	NP_001341739.1:p.Asp498=
NR_148971.2:n.1916_1921delinsACCGGG
NM_000142.5:c.1490_1495delinsACCGGG MANE Select	NP_000133.1:p.Asp497=
NM_001163213.2:c.1496_1501delinsACCGGG	NP_001156685.1:p.Asp499=
NM_022965.4:c.1154_1159delinsACCGGG	NP_075254.1:p.Asp385=